We thank Timothy F. Sharbel (IPK Gatersleben) for providing Boechera divaricarpa seeds and Sharon Kessler (University of Oklahoma) for critical reading and proofreading. Work on cell type-specific transcriptome analyses to study gametophyte development and apomixis in UG&#180;s laboratory is supported by the University of Z&#252;rich, by a fellowship of the "Deutsche Forschungsgemeinschaft" and the Marie Curie project IDEAGENA to AS, by grants from the "Staatssekretariat f&#252;r Bildung und Forschung" in the framework of COST action FA0903 (to UG and AS) and the Swiss National Foundation (to UG).

Note: This protocol describes tissue preparation, laser assisted microdissection, and RNA extraction for transcriptional profiling. Always use gloves throughout all steps of the protocol. Study and consider the safety instructions for each chemical used. In particular, keep in mind that Xylol is harmful and can penetrate gloves and that methanol is toxic. For all instruments used, please refer to user manuals accordingly.
1. Removal of RNAse Activity from Glassware and Other Equipment
<ol>
	<li>Prior to use, wrap any glassware&#160; in aluminum foil prior to baking for ~ 8 hr at 180 &#176;C to ensure RNAse free quality.</li>
	<li>Treat any metal surfaces (e.g., pair of tweezers) as well as the work bench and the heating plate with an appropriate RNAse decontamination solution. Afterwards, wash the surfaces with RNAse-free water to remove the decontamination solution. Subsequently, clean the surfaces further with 70% EtOH.</li>
	<li>Use all plastic consumables (e.g., tubes) brand-new without any pretreatment. If available, use plastic consumables that are certified to be RNAse free.</li>
</ol>
2. Tissue Fixation
<ol>
	<li>Prepare 10 ml of farmer&#39;s fixative (3:1; v/v ethanol:acetic acid) in a fresh 15 ml tube on ice. (Always prepare fresh Farmer&#39;s fixative before use). As an alternative, the non-crosslinking fixative ethanol:acetic acid (5:1; v/v) can be used 18.</li>
	<li>Use a fine pair of tweezers to collect buds at the developmental stage of interest. Immediately submerge buds in the ice-cold fixative. Use 10 ml of fixative for the fixation of ~ 20 buds or flowers from Arabidopsis or Boechera. Note: When using plant species with larger flowers it is recommended to dissect the flowers with a razor blade to generate smaller pieces prior to fixation.
	<ol>
		<li>In order to obtain mature gametophytes, emasculate the 2 - 3 largest flower buds of the inflorescence 2 days prior to harvest.</li>
	</ol>
	</li>
	<li>Fill the bottom of an exsiccator with ice. Open the tubes containing the samples, e.g., flowers, and place them on ice, either by directly putting them into the ice in a way that they cannot fall over or by using an appropriate holder. Vacuum infiltrate for 15 min prior to release of the vacuum.
	<ol>
		<li>Repeat the vacuum infiltration once for 15 min.</li>
	</ol>
	</li>
	<li>Release the vacuum and store overnight (~ 12 hr) on ice. Cover the ice bucket with a lid or aluminum foil and store the bucket in a 4 &#176;C room or refrigerator in order to prevent the ice from thawing. Note: Prolonging the fixation time is not recommended.</li>
</ol>
3. Tissue Embedding, Thin Sectioning, and Mounting on Slides for LAM
<ol>
	<li>Tissue embedding.
	<ol>
		<li>Exchange the fixative to 70% ethanol prepared with pure ethanol and RNAse free water. Leave the samples on ice until further processing. Start embedding of the samples the same day. In case no tissue-processing machine is available, proceed to manual embedding as described elsewhere 9,11 and continue with step 3.1.11.</li>
		<li>Gently transfer the samples to tissue embedding cassettes with a pair of tweezers. Firmly close the cassettes. CRITICAL STEP: Avoid even partial drying of the sample during this step. Avoid squeezing of samples with the tweezers. 
		Note: To label the cassettes a pencil should be used, ideally by writing on the inclined surface of the cassette.</li>
		<li>Store the embedding cassette loaded with the buds or flowers in 70% ethanol until all material is transferred to cassettes and the embedding machine can be loaded. For this purpose, use a glass staining trough filled with 70% ethanol.</li>
		<li>Remove the basket of the tissue processor from the retort of the machine and transfer the embedding cassettes to the basket with the inclined surfaces facing the top and in the same direction. CRITICAL STEP: Perform this quickly to prevent any drying of the tissues. If processing many embedding cassettes at once, place the basket into an appropriate RNAse free container filled with 70% ethanol prior to loading the samples.</li>
		<li>Put the lid on the basket and put the basket back into the retort. Close the retort. 
		Note: The tissue processor automatically dehydrates the samples, changes the solvent to Xylol, and does the infiltration with melted paraffin wax. Typically, this is done overnight.</li>
		<li>Start the program of the tissue processor. Recommended standard settings are 1 hr 70% EtOH, three times 1 hr 90% EtOH, three times 1 hr 100% EtOH, two times 1 hr 100% Xylol, one time 1 hr 15 min 100% Xylol at room temperature, followed by infiltration with paraffin wax two times for 1 hr and one time for 3 hr at 56 &#176;C 11. 
		Note: To ensure that the blocking station is ready with the wax melted, switch the machine on several hours before start or use the timer function to select the approximate starting time. 
		Note: In case the tissue cannot be processed immediately afterwards, longer incubation times in paraffin wax at 56 &#176;C are possible instead of the 3 hr at 56 &#176;C. Refer to the user manual of the instrument. Typically, the cassettes with tissues will automatically remain in melted wax until the &#34;empty retort&#34; command is approved. If the wax is not melted when starting the tissue processor, the retort is filled with 70% ethanol and the program remains on hold until ready to start.</li>
		<li>Empty the retort and immediately transfer the samples to a paraffin wax bath at 56 &#176;C in a blocking station. Remove the lid from the basket and cover the paraffin bath of the blocking station with its lid.</li>
		<li>Pile as many fresh balancing trays on the surface of the blocking station heated to 56 &#176;C as there are cassettes in the basket. 
		Note: An ethanol-resistant permanent marker can be used to label the bottom of the balancing trays. Acetone-resistant permanent markers are not recommended.</li>
		<li>Using the blocking station, fill a pre-warmed fresh plastic balancing tray with melted paraffin wax at 56 &#176;C. Lift the lid of the paraffin bath, pick up one cassette only at a time and transfer the samples from the cassettes to the liquid paraffin wax at 56 &#176;C in the balancing tray using a pair of tweezers. 
		CRITICAL STEP: Avoid any hardening of the wax surrounding the sample while handling the cassette by working quickly.
		<ol>
			<li>Position all samples according to the needs using a preparation needle before hardening of the wax. Typically, several flowers are arranged in a balancing tray individually spaced about 1 cm in each direction.</li>
			<li>Repeat step 3.1.9 until all samples are transferred.</li>
		</ol>
		</li>
		<li>Place the basket back to the tissue processor and clean the retort using an appropriate program (refer to user manual).</li>
		<li>Switch off tissue processor and blocking station. Continue with step 3.1.13.</li>
		<li>In case no tissue infiltration machine and no embedding station is available, use a heating oven to melt paraffin wax at 56 &#176;C. On the bench, fill the melted wax in plastic balancing trays, transfer the samples to the wax, and use preparation needles to position the samples.</li>
		<li>Allow the paraffin wax to harden at room temperature for ~ 1 - 3 hr before storing the samples at 4 &#176;C. Samples can subsequently be processed freshly or stored for up to several months.</li>
	</ol>
	</li>
	<li>Preparation of thin sections and slides for LAM.
	<ol>
		<li>On a light table illuminating the wax block from below, remove the paraffin wax with the samples from the surrounding plastic trays. Dissect out a squared wax block containing the tissue, e.g., a bud or flower, using an RNAse free razor blade. To this aim, always orient the samples towards the top of the wax block (also see Figure 1).
		<ol>
			<li>Prepare wax blocks of all samples that should be used for LAM at a time.</li>
		</ol>
		</li>
		<li>Mount the blocks to process embedding cassettes filled with hardened paraffin wax: melt a small piece or droplet of paraffin wax on the tip of an appropriate spatula using an Ethanol lamp and use the hot wax to fix the block on the support (with the embedded tissues on top).
		<ol>
			<li>Allow the wax to harden for at least 20 min at 4 &#176;C.</li>
		</ol>
		</li>
		<li>Remove surplus wax surrounding the sample with a razor blade on the light table. Make sure to keep a square surface with parallel edges (see Figure 1).</li>
		<li>Set the heating plate to 42 &#176;C.</li>
		<li>Safely mount the samples to the microtome and prepare 6 - 10 &#181;m thick sections. Refer to the manufacturer&#39;s instructions for using the microtome. Note: While thinner sections will often give better structural resolution, larger amount of RNA of higher quality can be obtained with thicker sections. For the cells of Boechera mature gametophytes we use 7 &#181;m as the default. Moving rather slowly with the samples over the microtome knife often results in better histology.</li>
		<li>Always transfer the paraffin ribbons at a length of approximately 10 - 15 cm into a plastic box with a black cardboard at the bottom before positioning them in LAM slides.</li>
		<li>If possible, pre-select the parts of the paraffin strips containing the cell- or tissue types of interest, e.g., ovules, under a dissecting-scope and discard the rest.</li>
	</ol>
	</li>
	<li>Preparation of the slides for LAM.
	<ol>
		<li>Place the required amount of metal-framed slides (typically 5 - 10) with the flat surface on top on the heating plate.</li>
		<li>Pipet ~ 1 - 2 ml of RNAse free water on the plastic part of the slide. Using a razor blade, cut the paraffin ribbons in short pieces of about 4 - 5 cm long enough to span the plastic windows. Use a pair of tweezers and a preparation needle to ideally place the paraffin strips parallel to each other on the plastic windows of the slides. Carefully lift the slide at one end to remove the water and place the slides back.
		<ol>
			<li>Alternatively, place the heating plate under a chemical hood. Apply a small volume of methanol to the plastic part of the slide just sufficient to wet the surface (this can cause a slight corrugation of the slides). Place the paraffin strips on the slides. 
			Note: For reasons of toxicity, avoid use of methanol if possible. However, the use of methanol at this step does improve the RNA quality in case the quality achieved by mounting on water is not sufficient. It is worthwhile testing these alternatives at the start of a new project, as the RNA quality achieved varies with cell type and species under investigation.</li>
		</ol>
		</li>
		<li>Dry the slides overnight on the heating plate at 42 &#176;C for ~ 12 hr. Cover the heating plate with a plastic lid that does not touch the slides. Ensure that the plastic lid does not prevent the exchange of air. To this aim the lid can be placed on pipet boxes or similar to be lifted.
		<ol>
			<li>Alternatively, reduce the drying time to a minimum of two hours or until the tissue appears totally dry. The reduction of time from slicing to collection may improve RNA quality.</li>
		</ol>
		</li>
		<li>Under a chemical hood, de-wax the slides 2 times for 10 min in Xylol using appropriate slide holders. Make sure to fully submerge the plastic part of each slide only but to allow removal of the slide by touching the broader end of the metal frame that is kept dry.</li>
		<li>Allow the slides to dry for ~ 10 min under the chemical hood prior to LAM. 
		Note: Slides not immediately processed can be placed back on the heating plate at 42 &#176;C with the tissue facing up for up to a few hours. This will prevent any humidity from compromising RNA quality until further processing.</li>
	</ol>
	</li>
</ol>
4. Laser-assisted Microdissection (LAM)
Note: The procedure for LAM will vary with the instrument used. Certain details of this protocol are adapted to a specific instrument and the technology of collecting the samples on a cap making use of electrostatic forces. In addition, details might vary even between different versions of the software. Please refer to manufacturer&#39;s instructions and user handbooks for a detailed description and specific instructions on instrument and software.
<ol>
	<li>Switch on the devices for LAM (computer, microscope, laser control box).</li>
	<li>Start the program steering the microscope and laser.</li>
	<li>Switch on the laser by pressing the corresponding button on the control box.</li>
	<li>Place a cap (0.5 ml, without diffusor) into the cap holder and position it in the instrument.</li>
	<li>Support the LAM slide with a glass slide for microscopy. Ensure that the flat surface of the slide with the tissue attached faces the glass slide.</li>
	<li>Place the slide in the instrument with the glass slide underneath.</li>
	<li>Select the 4X Objective. In the program, select to move the cap to the &#34;up&#34; position and proceed to make a scan of the slide.</li>
	<li>Search through the slide and identify the structures of interest. Pinpoint and save their positions on the slide to be able to move back to the exact position for the cutting step.</li>
	<li>Select the appropriate objective (e.g. 40X or 60X).</li>
	<li>If needed, adjust laser speed, focus, and laser power, and also calibrate the stage movement by referring to the user manual of the instrument. Once an account is set up for the specific tissue of interest, the settings can be reused.</li>
	<li>Verify the laser position by a single shot by pressing the &#34;laser shot&#34; button of the program, ideally in a part of the membrane without tissue.
	<ol>
		<li>If required, calibrate the laser position by following the manufacturer&#39;s instructions for the instrument.</li>
	</ol>
	</li>
	<li>Verify the calibration of the objective by moving an obvious structure to all four corners of the software window on the monitor, keeping the right mouse button pressed. Check that the position of the hand with respect to the obvious structure is the same in all four corners. Otherwise calibrate the objectives following the software manual.</li>
	<li>With the cap in the &#39;down&#39; position, use the &#39;hand-pen&#39; tool to mark the borders of the cell type or tissue of interest, e.g., the egg cell. Dissect the cell of interest with the laser by pressing &#39;cut&#39;. Note: Often, sectioning needs to be repeated if the border around the cell was not entirely dissected at once. In this case, it is recommended to set the software to automatically do two repeats of the section as a standard.</li>
	<li>Lift the cap and move to the next saved position with the structure of interest. Repeat step 4.13 of the procedure to dissect the next cell sections until all cells of interest from one slide are collected. Make sure the cap is positioned in a way that the new section sticks to an empty position on the cap. 
	Note: It is recommended to isolate larger pieces of tissues (e.g., sections of whole flowers or parts of it) from each slide after the isolation of single cell sections on a fresh cap. These can be used for RNA quality control.</li>
	<li>Remove the slide and continue with the next slide by repeating steps 4.4 - 4.9 and 4.13 to 4.14.</li>
	<li>Repeat step 4.15 and related steps until the cell types of interest from all slides have been isolated. Note: It is not recommended to harvest for longer than ~ 4 - 5 hr on the same cap.</li>
	<li>Visually inspect the cap surface after LAM to exclude unspecific contaminations of the sample. While the non-dissected tissues are protected with the foil, dust can stick to the surface due to electrostatic adhesion.
	<ol>
		<li>To visually inspect the cap, remove the slide from the instrument. Place the cap holder in the &#39;down&#39; position and inspect the surface with the 4X objective.</li>
		<li>In case small pieces of dust are visible, remove them with a small (2 &#181;l) pipette tip. Alternatively, mount the slide back on the instrument, place the cap on a free part of the slide (no tissues), and completely destroy the contamination using the laser.</li>
	</ol>
	</li>
	<li>Close caps and freeze the dry sections at -80 &#176;C until further use. If required, samples can be stored for up to several weeks. However, proceeding quickly at this step is recommended.</li>
</ol>
5. RNA Isolation and Quality Control
Note: RNA can be isolated by any method suitable for small amounts of RNA. In this protocol the use of an RNA isolation kit specified for small amounts of RNA is described. Follow the manufacturer&#39;s instructions.
<ol>
	<li>Use the tubes with the sample attached to the cap either directly or after removal from -80 &#176;C.
	<ol>
		<li>Open the tubes and carefully pipet 11 &#181;l of extraction buffer to the wall of each tube using filter tips. Change tips between samples.</li>
		<li>Close the lid and shake the extraction buffer down to the cap of the tube.</li>
		<li>Place the tubes with the cap down in a heating oven preheated to 42 &#176;C. Incubate for 30 min following the manufacturer&#39;s instructions.</li>
	</ol>
	</li>
	<li>Follow the manufacturer&#39;s instructions for column preparation and collecting the extract at the bottom of the tubes.
	<ol>
		<li>If material from more than one cap needs to be combined into one sample, proceed with steps 5.1.1 - 5.1.2 individually for each tube/cap.</li>
		<li>Afterwards, pool the extracts for one sample in one tube and measure the amount of pooled extract with a pipette prior to addition of an equivalent amount of EtOH (see manufacturer&#39;s instructions).</li>
		<li>Ensure that the amount of EtOH added before loading the column is equal to the volume of the pooled extract.</li>
		<li>After RNA precipitation with EtOH, proceed quickly to the loading of the columns following manufacturer&#39;s instructions. Continue the protocol with the 100 x g centrifugation step.</li>
		<li>After the contents of each collecting tube have been passed through the column, perform a 16,000 x g centrifugation step for 30 sec to remove the flow-through following manufacturer&#39;s instructions.</li>
		<li>Continue with RNA extraction and purification following manufacturer&#39;s instructions.</li>
		<li>After loading of the elution buffer to the column allow the column to incubate for 1 min. Continue to load the tubes into the centrifuge following the instructions in the manufacturer&#39;s instructions. Note: An additional centrifugation step for 1 min at 100 x g prior to elution as indicated in the protocol can increase the efficiency of elution.</li>
	</ol>
	</li>
	<li>Extract RNA from the controls (larger tissue sections) for RNA quality control following steps 5.1 to 5.2.7 of this protocol.</li>
	<li>For RNA quality control load 1 &#181;l undiluted total RNA of each control sample on the Bioanalyzer using an RNA Pico Chip following the manufacturer&#39;s instructions. 
	Note: The extracted RNA can be used for linear amplification and transcriptome analysis using microarrays or RNA-Seq 7,11,13,14. Ideally, the quality control should indicate an RNA Integrity Number (RIN) of at least 7. A number of suppliers provide suitable kits for amplification, suitable examples are given in 9.</li>
</ol>

<ol>
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The authors have nothing to disclose.

The Protocol is Suitable for Different Cell and Tissue Types
LAM combined with transcriptome analyses by microarrays or RNA-Seq is a valuable tool to gain insights into the specific patterns of gene activity regulating developmental or physiological processes 7-11,13,14. However, the suitability of this method for any given cell type is critically dependent on structural issues. The cell needs to be clearly visible and unambiguously identifiable in the dry sections ...

In transcriptional studies done at the tissue level, the transcriptomes of highly specialized but rare cell types are often masked by the more abundant surrounding cells. An example for such highly specialized cell types are the cells of the female reproductive lineage (germline) in plants. The female germline is specified within developing ovules, the precursors of seeds inside the gynoecium of the flower 1,2. The megaspore mother cell (MMC) is the first cell of the female germline. It undergoes meiosis to form a tetrad of reduced megaspores. Typically, only one of these megaspores survives and divides mitotically without cytokinesis, i.e., in a syncytium. These mitoses are followed by cellularization to form the mature gametophyte, which typically consists of four cell types: three antipodals, two synergid cells, the egg, and the central cell. The egg and central cells are the female gametes that get fertilized by two sperm cells during double fertilization to give rise to the embryo and endosperm of the developing seed 1,2. In the sexual model system Arabidopsis thaliana, only ~ 50 seeds develop per flower while about 50 - 80 seeds develop per flower in the closely related genus Boechera. Thus, the female germline consists of only a few highly specialized cell types, making it an excellent model to study developmental processes, such as cell specification and differentiation.
Moreover, insights into the gene regulatory processes governing plant reproduction can be of applied value. In plants, both sexual and asexual reproduction through seeds (apomixis) can occur. While sexual reproduction generates genetic diversity in a population, apomixis leads to the formation of clonal offspring that is genetically identical to the mother plant. Therefore, apomixis has great potential for applications in agriculture and seed production, as even complex maternal genotypes can be maintained unaltered over several generations 3,4,5. Because apomixis does not naturally occur in any major crop species, the engineering of apomixis in crops is of great interest 3,4,5. However, this long-term goal is difficult to achieve because the underlying genetic and molecular basis of apomixis is not understood in sufficient detail 6.
To gain insights into the transcriptional basis governing apomictic reproduction, cell type-specific transcriptional profiling using laser-assisted microdissection (LAM) and next generation sequencing (NGS) represents a very powerful approach 7,8. LAM has first been established for animal and biomedical research. In the past few years LAM has also been applied to plant biology 6,9,10. In contrast to other methods allowing profiling of individual cell and tissue types, LAM does not require the generation of marker lines 6,9,10. Therefore, it can be applied to any cell or tissue type without prior molecular knowledge. Another advantage of LAM is that it can be applied to any cell type as long as the cell can be recognized in dry sections based on position and/or structural features. LAM has the additional advantage that fixed tissues are used, which prevents changes of the transcriptional profile during processing.
The tissue of interest, e.g., floral tissue, is fixed in a non-crosslinking fixative prior to embedding in paraffin wax. Embedding in paraffin wax can be done manually, following established protocols 9,11. However, the use of an automated tissue processor for dehydration and infiltration with the wax generally results in higher reproducibility in terms of the conservation of RNA quality and tissue morphology. The alternative strategy of embedding tissues in resin has also been successfully used for cell type-specific analyses by LAM 8. However, the use of an automated tissue processor for embedding in wax is very time efficient, as many samples can be processed at once requiring a minimum of hands-on time. While typically no significant loss of RNA quality occurs during fixation and embedding, the preparation of thin sections with the microtome and, in particular, the mounting on the frameslides used for LAM remains a critical step for preservation of RNA quality. This has previously been noted and the use of a tape transfer system has been described to result in better RNA quality at this step 12. However, this adds an additional time-consuming step during preparation of the slides and also requires special equipment. The optimized protocol described below reproducibly produces RNA that is of sufficient quality for transcriptional profiling with GeneCHIPs and Next Generation Sequencing (NGS) approaches 7,11,13,14. In addition, with the laser microdissection microscope used, a high purity of the isolated cell types is routinely produced 7,11,13,14.
The genus Boechera is an excellent model system for studying the key steps of apomictic reproduction. In Boechera, a variety of different sexual and apomictic accessions have been identified and can be used for comparative analyses 15,16,17. In a comparison of cell type-specific transcriptomes of cells from the female germline from sexual Arabidopsis and apomictic Boechera, we identified genes and pathways that are differentially expressed, thereby identifying new aspects of the regulatory processes governing apomixis 7. In addition, this study verified the suitability of LAM for cell type-specific transcriptional analyses of small and rare cell types. We have already used this protocol for the analysis of different cell types in a variety of plant species, but species- and tissue-specific modifications to the protocol may be required in certain cases.

<table>
	<tbody>
		<tr>
			<td>Ethanol</td>
			<td>VWR</td>
			<td>1,009,861,000</td>
			<td>absolute EMPROVE Ph Eur,BP,USP</td>
		</tr>
		<tr>
			<td>15 ml falcon centrifuge tubes</td>
			<td>VWR</td>
			<td>62406-200</td>
			<td></td>
		</tr>
		<tr>
			<td>2100 Bioanalyzer</td>
			<td>Agilent</td>
			<td>G2939AA</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetic Acid</td>
			<td>Applichem</td>
			<td>A3686,2500</td>
			<td>100% Molecular biology grade</td>
		</tr>
		<tr>
			<td>Ambion Nuclease free water</td>
			<td>life technologies</td>
			<td>AM9932</td>
			<td></td>
		</tr>
		<tr>
			<td>ASP200 S</td>
			<td>Leica</td>
			<td>14048043624</td>
			<td>tissue processor&#160;</td>
		</tr>
		<tr>
			<td>black cardboard</td>
			<td></td>
			<td></td>
			<td>can be purchased in special paper shops</td>
		</tr>
		<tr>
			<td>DNA- and RNAse-free Frame Slides</td>
			<td>Micro Dissect GmbH</td>
			<td></td>
			<td>1,4 &#181;m PET-membrane; can also be purchased from Leica</td>
		</tr>
		<tr>
			<td>Dumond Forceps</td>
			<td>Actimed</td>
			<td>0208-5SPSF-PS</td>
			<td></td>
		</tr>
		<tr>
			<td>ethanol lamp</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>exsiccator</td>
			<td>Sigma-Aldrich</td>
			<td>Z354074-1EA</td>
			<td>Nalgene Vaccuum Dessicator or similar equipment</td>
		</tr>
		<tr>
			<td>filter tips 10&#160; &#181;l&#160;</td>
			<td>Axon Lab AG</td>
			<td>AL60010</td>
			<td>can be replaced by similar tips</td>
		</tr>
		<tr>
			<td>filter tips 1000&#160; &#181;l&#160;</td>
			<td>Axon Lab AG</td>
			<td>AL60010</td>
			<td>can be replaced by similar tips</td>
		</tr>
		<tr>
			<td>filter tips 20&#160; &#181;l&#160;</td>
			<td>Axon Lab AG</td>
			<td>AL60020</td>
			<td>can be replaced by similar tips</td>
		</tr>
		<tr>
			<td>filter tips 200&#160; &#181;l&#160;</td>
			<td>Axon Lab AG</td>
			<td>AL60200</td>
			<td>can be replaced by similar tips</td>
		</tr>
		<tr>
			<td>forceps precision</td>
			<td>VWE</td>
			<td>232-1221</td>
			<td></td>
		</tr>
		<tr>
			<td>glass slide holder</td>
			<td>Huber &#38; Co.AG</td>
			<td>10.0540.01</td>
			<td>F&#228;rbek&#228;sten nach Hellendahl</td>
		</tr>
		<tr>
			<td>glass staining trough</td>
			<td>Huber &#38; Co.AG</td>
			<td>10.0570.01</td>
			<td>F&#228;rbekasten</td>
		</tr>
		<tr>
			<td>Heated Paraffin Embedding Module Leica</td>
			<td>Leica</td>
			<td>Leica EG 1150 H</td>
			<td>blocking station, similar devises are suitable</td>
		</tr>
		<tr>
			<td>Heating and Drying Table</td>
			<td>Medax</td>
			<td>15501</td>
			<td>other models and/or suppliers are suitable</td>
		</tr>
		<tr>
			<td>ice bucket</td>
			<td>VWR ice bucket with lid&#160;</td>
			<td>10146-184</td>
			<td>similar buckets equally suitable</td>
		</tr>
		<tr>
			<td>light table</td>
			<td>UVP An Analytical Jena Company</td>
			<td>TW-26&#160;</td>
			<td>white light transluminator</td>
		</tr>
		<tr>
			<td>microscope slide</td>
			<td>Thermo Scientific</td>
			<td>10143562CE</td>
			<td>cut edges</td>
		</tr>
		<tr>
			<td>microtome blade</td>
			<td>Thermo Scientific</td>
			<td>FEAHS35</td>
			<td>S35 microtome blade disposable</td>
		</tr>
		<tr>
			<td>MMI Cell Cut Plus Instrument</td>
			<td>MMI (Molecular Machines and Industries)</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Non-stick, RNAse free Microfuge tubes, 2ml</td>
			<td>life technologies</td>
			<td>AM12475</td>
			<td></td>
		</tr>
		<tr>
			<td>Paraplast X-TRA</td>
			<td>Roth</td>
			<td>X882.2</td>
			<td>for histology</td>
		</tr>
		<tr>
			<td>PicoPure RNA Isolation Kit</td>
			<td>life technologies</td>
			<td>KIT0204</td>
			<td>Arcturus PicoPure RNA Isolation Kit</td>
		</tr>
		<tr>
			<td>plastic balancing trays</td>
			<td>Semadeni AG</td>
			<td>2513</td>
			<td></td>
		</tr>
		<tr>
			<td>plastic box</td>
			<td>Semadeni AG</td>
			<td>2971</td>
			<td>Plastikdose PS</td>
		</tr>
		<tr>
			<td>plastic lid for heating plate</td>
			<td></td>
			<td></td>
			<td>homemade</td>
		</tr>
		<tr>
			<td>preparation needle</td>
			<td>VWR</td>
			<td>631-7159</td>
			<td></td>
		</tr>
		<tr>
			<td>RNA 6000 Pico Kit</td>
			<td>Agilent</td>
			<td>5067-1513</td>
			<td></td>
		</tr>
		<tr>
			<td>RNAse free microfuge tubes</td>
			<td>life technologies</td>
			<td>AM12400</td>
			<td></td>
		</tr>
		<tr>
			<td>RNAse ZAP Decontamination Solution</td>
			<td>life technologies</td>
			<td>AM9780</td>
			<td></td>
		</tr>
		<tr>
			<td>Semi-automated Rotary Microtome&#160;</td>
			<td>Leica</td>
			<td>RM2245</td>
			<td>similar devises are equally suitable</td>
		</tr>
		<tr>
			<td>Tissue Loc&#160; Histo Screen Cassettes</td>
			<td>Thermo Scientific</td>
			<td>C-1000_AQ</td>
			<td>similar cassettes of other suppliers are suitable</td>
		</tr>
		<tr>
			<td>Tubes with adhesive lid, without diffusor 500 &#181;l&#160;</td>
			<td>MMI (Molecular Machines and Industries)</td>
			<td>50204</td>
			<td></td>
		</tr>
		<tr>
			<td>Xylol (Isomere) ROTIPURAN</td>
			<td>VWR</td>
			<td>4436.2</td>
			<td>min. 99 %, p.a.,ACS, ISO SP</td>
		</tr>
		<tr>
			<td>process embedding cassettes</td>
			<td>Leica</td>
			<td>14039440000</td>
			<td>Leica Jet Cassette I without lid</td>
		</tr>
		<tr>
			<td>Universal Oven</td>
			<td>Memmert</td>
			<td>UF55</td>
			<td>other models and/or suppliers are suitable</td>
		</tr>
	</tbody>
</table>

laser-assisted microdissection (lam) as a tool for transcriptional profiling of individual cell types

The understanding of developmental processes at the molecular level requires insights into transcriptional regulation, and thus the transcriptome, at the level of individual cell types. While the methods described here are generally applicable to a wide range of species and cell types, our research focuses on plant reproduction. Plant cultivation and seed production is of crucial importance for human and animal nutrition. A detailed understanding of the regulatory networks that govern the formation of the reproductive lineage (germline) and ultimately of seeds is a precondition for the targeted manipulation of plant reproduction. In particular, the engineering of apomixis (asexual reproduction through seeds) into crop plants promises great improvements, as it leads to the formation of clonal seeds that are genetically identical to the mother plant. Consequently, the cell types of the female germline are of major importance for the understanding and engineering of apomixis. However, as the corresponding cells are deeply embedded within the floral tissues, they are very difficult to access for experimental analyses, including cell-type specific transcriptomics. To overcome this limitation, sections of individual cells can be isolated by laser-assisted microdissection (LAM). While LAM in combination with transcriptional profiling allows the identification of genes and pathways active in any cell type with high specificity, establishing a suitable protocol can be challenging. Specifically, the quality of RNA obtained after LAM can be compromised, especially when small, single cells are targeted. To circumvent this problem, we have established a workflow for LAM that reproducibly results in high RNA quality that is well suitable for transcriptomics, as exemplified here by the isolation of cells of the female germline in apomictic Boechera. In this protocol, procedures are described for tissue preparation and LAM, also with regard to RNA extraction and quality control.

Sample Preparation and LAM are done in Consecutive Steps
A number of consecutive steps are required to prepare RNA for transcriptional analysis from selected cell types by LAM (Figure 1). This starts with the harvest of the flowers and immediate fixation to ensure that the RNA population remains unchanged after harvest. The tissue is embedded, sectioned, and mounted on slides. This allows the is...

Watch this Scientific Journal Video about Laser-assisted Microdissection LAM as a Tool for Transcriptional Profiling of Individual Cell Types at JoVE.com

Laser-assisted Microdissection LAM as a Tool for Transcriptional Profiling of Individual Cell Types

Here we present a protocol for laser-assisted microdissection of specific plant cell types for transcriptional profiling. While the protocol is suitable for different species and cell types, the focus is on highly inaccessible cells of the female germline important for sexual and apomictic reproduction in the crucifer genus Boechera.

Laser-assisted Microdissection (LAM) as a Tool for Transcriptional Profiling of Individual Cell Types

The understanding of developmental processes at the molecular level requires insights into transcriptional regulation, and thus the transcriptome, at the ...

laser-assisted-microdissection-lam-as-tool-for-transcriptional

Universidad de Cartagena UDEC

Research

JoVE Journal

Biology

9.2K Views.  University of Zürich & Zürich-Basel Plant Science Center. Here we present a protocol for laser-assisted microdissection of specific plant cell types for transcriptional profiling. While the protocol is suitable for different species and cell types, the focus is on highly inaccessible cells of the female germline important for sexual and apomictic reproduction in the crucifer genus Boechera. 

Video: Laser-assisted Microdissection LAM as a Tool for Transcriptional Profiling of Individual Cell Types

Laser Capture Microdissection of Mammalian Tissue

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or formalin-fixed, paraffin-embedded tissue sections. LMD techniques rely on a thermo labile membrane placed either on top of, or underneath, the tissue section. In one method, focused laser energy is used to melt the membrane onto the underlying cells, which can then be lifted out of the tissue section. In the other, the laser energy vaporizes the foil along a path "drawn" on the tissue, allowing the selected cells to fall into a collection device. Each technique allows the selection of cells with a minimum resolution of several microns. DNA, RNA, protein, and lipid samples may be isolated and analyzed from micro-dissected samples. In this video, we demonstrate the use of the Leica AS-LMD laser microdissection instrument in seven segments, including an introduction to the principles of LMD, initializing the instrument for use, general considerations for sample preparation, mounting the specimen and setting up capture tubes, aligning the microscope, adjusting the capture controls, and capturing tissue specimens. Laser-capture micro-dissection enables the investigator to isolate samples of pure cell populations as small as a few cell-equivalents. This allows the analysis of cells of interest that are free of neighboring contaminants, which may confound experimental results.

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or ...

Single Cell Transcriptional Profiling of Adult Mouse Cardiomyocytes

While numerous studies have examined gene expression changes from homogenates of heart tissue, this prevents studying the inherent stochastic variation between cells within a tissue. Isolation of pure cardiomyocyte populations through a collagenase perfusion of mouse hearts facilitates the generation of single cell microarrays for whole transcriptome gene expression, or qPCR of specific targets using nanofluidic arrays. We describe here a procedure to examine single cell gene expression profiles of cardiomyocytes isolated from the heart. This paradigm allows for the evaluation of metrics of interest which are not reliant on the mean (for example variance between cells within a tissue) which is not possible when using conventional whole tissue workflows for the evaluation of gene expression (Figure 1). We have achieved robust amplification of the single cell transcriptome yielding micrograms of double stranded cDNA that facilitates the use of microarrays on individual cells. In the procedure we describe the use of NimbleGen arrays which were selected for their ease of use and ability to customize their design. Alternatively, a reverse transcriptase - specific target amplification (RT-STA) reaction, allows for qPCR of hundreds of targets by nanofluidic PCR. Using either of these approaches, it is possible to examine the variability of expression between cells, as well as examining expression profiles of rare cell types from within a tissue. Overall, the single cell gene expression approach allows for the generation of data that can potentially identify idiosyncratic expression profiles that are typically averaged out when examining expression of millions of cells from typical homogenates generated from whole tissues.

Single cell expression profiling allows the detailed gene expression analysis of individual cells. We describe methods for the isolation of cardiomyocytes, and preparing the resulting lysates for either whole transcriptome microarray or qPCR of specific targets.

While numerous studies have examined gene expression changes from homogenates of heart tissue, this prevents studying the inherent stochastic variation ...

Electroantennographic Bioassay as a Screening Tool for Host Plant Volatiles

Plant volatiles play an important role in plant-insect interactions. Herbivorous insects use plant volatiles, known as kairomones, to locate their host plant.1,2 When a host plant is an important agronomic commodity feeding damage by insect pests can inflict serious economic losses to growers. Accordingly, kairomones can be used as attractants to lure or confuse these insects and, thus, offer an environmentally friendly alternative to pesticides for insect control.3 Unfortunately, plants can emit a vast number volatiles with varying compositions and ratios of emissions dependent upon the phenology of the commodity or the time of day. This makes identification of biologically active components or blends of volatile components an arduous process. To help identify the bioactive components of host plant volatile emissions we employ the laboratory-based screening bioassay electroantennography (EAG). EAG is an effective tool to evaluate and record electrophysiologically the olfactory responses of an insect via their antennal receptors. The EAG screening process can help reduce the number of volatiles tested to identify promising bioactive components. However, EAG bioassays only provide information about activation of receptors. It does not provide information about the type of insect behavior the compound elicits; which could be as an attractant, repellent or other type of behavioral response. Volatiles eliciting a significant response by EAG, relative to an appropriate positive control, are typically taken on to further testing of behavioral responses of the insect pest. The experimental design presented will detail the methodology employed to screen almond-based host plant volatiles4,5 by measurement of the electrophysiological antennal responses of an adult insect pest navel orangeworm (Amyelois transitella) to single components and simple blends of components via EAG bioassay. The method utilizes two excised antennae placed across a "fork" electrode holder. The protocol demonstrated here presents a rapid, high-throughput standardized method for screening volatiles. Each volatile is at a set, constant amount as to standardize the stimulus level and thus allow antennal responses to be indicative of the relative chemoreceptivity. The negative control helps eliminate the electrophysiological response to both residual solvent and mechanical force of the puff. The positive control (in this instance acetophenone) is a single compound that has elicited a consistent response from male and female navel orangeworm (NOW) moth. An additional semiochemical standard that provides consistent response and is used for bioassay studies with the male NOW moth is (Z,Z)-11,13-hexdecadienal, an aldehyde component from the female-produced sex pheromone.6-8

A method to rapidly screen host plant volatiles by measurement of the electrophysiological response of adult navel orangeworm (Amyelois transitella) antennae to single components and blends via electroantennographic analysis is demonstrated.

Plant volatiles play an important role in plant-insect interactions. Herbivorous insects use plant volatiles, known as kairomones, to locate their host ...

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

Extensive research has provided ample evidences suggesting that protein folding in the cell is a co-translational process1-5. However, the exact pathway that polypeptide chain follows during co-translational folding to achieve its functional form is still an enigma. In order to understand this process and to determine the exact conformation of the co-translational folding intermediates, it is essential to develop techniques that allow the isolation of RNCs carrying nascent chains of predetermined sizes to allow their further structural analysis.
SecM (secretion monitor) is a 170 amino acid E. coli protein that regulates expression of the downstream SecA (secretion driving) ATPase in the secM-secA operon6. Nakatogawa and Ito originally found that a 17 amino acid long sequence (150-FSTPVWISQAQGIRAGP-166) in the C-terminal region of the SecM protein is sufficient and necessary to cause stalling of SecM elongation at Gly165, thereby producing peptidyl-glycyl-tRNA stably bound to the ribosomal P-site7-9. More importantly, it was found that this 17 amino acid long sequence can be fused to the C-terminus of virtually any full-length and/or truncated protein thus allowing the production of RNCs carrying nascent chains of predetermined sizes7. Thus, when fused or inserted into the target protein, SecM stalling sequence produces arrest of the polypeptide chain elongation and generates stable RNCs both in vivo in E. coli cells and in vitro in a cell-free system. Sucrose gradient centrifugation is further utilized to isolate RNCs.
The isolated RNCs can be used to analyze structural and functional features of the co-translational folding intermediates. Recently, this technique has been successfully used to gain insights into the structure of several ribosome bound nascent chains10,11. Here we describe the isolation of bovine Gamma-B Crystallin RNCs fused to SecM and generated in an in vitro translation system.

We describe here a technique that is now routinely used to isolate stably bound ribosome nascent chain complexes (RNCs). This technique takes advantage of the discovery that a 17 amino acid long SecM "arrest sequence" can halt translation elongation in a prokaryotic (E. coli) system, when inserted into (or fused to the C-terminus) of virtually any protein.

Extensive research has provided ample evidences suggesting that protein folding in the cell is a co-translational process1-5. However, the exact pathway ...

Glycan Profiling of Plant Cell Wall Polymers using Microarrays

Plant cell walls are complex matrixes of heterogeneous glycans which play an important role in the physiology and development of plants and provide the raw materials for human societies (e.g. wood, paper, textile and biofuel industries)1,2. However, understanding the biosynthesis and function of these components remains challenging.
Cell wall glycans are chemically and conformationally diverse due to the complexity of their building blocks, the glycosyl residues. These form linkages at multiple positions and differ in ring structure, isomeric or anomeric configuration, and in addition, are substituted with an array of non-sugar residues. Glycan composition varies in different cell and/or tissue types or even sub-domains of a single cell wall3. Furthermore, their composition is also modified during development1, or in response to environmental cues4.
In excess of 2,000 genes have Plant cell walls are complex matrixes of heterogeneous glycans been predicted to be involved in cell wall glycan biosynthesis and modification in Arabidopsis5. However, relatively few of the biosynthetic genes have been functionally characterized 4,5. Reverse genetics approaches are difficult because the genes are often differentially expressed, often at low levels, between cell types6. Also, mutant studies are often hindered by gene redundancy or compensatory mechanisms to ensure appropriate cell wall function is maintained7. Thus novel approaches are needed to rapidly characterise the diverse range of glycan structures and to facilitate functional genomics approaches to understanding cell wall biosynthesis and modification.
Monoclonal antibodies (mAbs)8,9 have emerged as an important tool for determining glycan structure and distribution in plants. These recognise distinct epitopes present within major classes of plant cell wall glycans, including pectins, xyloglucans, xylans, mannans, glucans and arabinogalactans. Recently their use has been extended to large-scale screening experiments to determine the relative abundance of glycans in a broad range of plant and tissue types simultaneously9,10,11.
Here we present a microarray-based glycan screening method called Comprehensive Microarray Polymer Profiling (CoMPP) (Figures 1 &amp; 2)10,11 that enables multiple samples (100 sec) to be screened using a miniaturised microarray platform with reduced reagent and sample volumes. The spot signals on the microarray can be formally quantified to give semi-quantitative data about glycan epitope occurrence. This approach is well suited to tracking glycan changes in complex biological systems12 and providing a global overview of cell wall composition particularly when prior knowledge of this is unavailable.

A technique called Comprehensive Microarray Polymer Profiling (CoMPP) for the characterisation of plant cell wall glycans is described. This method combines the specificity of monoclonal antibodies directed to defined glycan-epitopes with a miniature microarray analytical platform allowing screening of glycan occurrence in a broad range of biological contexts.

Plant cell walls are complex matrixes of heterogeneous glycans which play an important role in the physiology and development of plants and provide the ...

Isolation and Culture of Individual Myofibers and their Satellite Cells from Adult Skeletal Muscle

Muscle regeneration in the adult is performed by resident stem cells called satellite cells. Satellite cells are defined by their position between the basal lamina and the sarcolemma of each myofiber. Current knowledge of their behavior heavily relies on the use of the single myofiber isolation protocol. In 1985, Bischoff described a protocol to isolate single live fibers from the Flexor Digitorum Brevis (FDB) of adult rats with the goal to create an in vitro system in which the physical association between the myofiber and its stem cells is preserved 1. In 1995, Rosenblattmodified the Bischoff protocol such that myofibers are singly picked and handled separately after collagenase digestion instead of being isolated by gravity sedimentation 2, 3. The Rosenblatt or Bischoff protocol has since been adapted to different muscles, age or conditions 3-6. The single myofiber isolation technique is an indispensable tool due its unique advantages. First, in the single myofiber protocol, satellite cells are maintained beneath the basal lamina. This is a unique feature of the protocol as other techniques such as Fluorescence Activated Cell Sorting require chemical and mechanical tissue dissociation 7. Although the myofiber culture system cannot substitute for in vivo studies, it does offer an excellent platform to address relevant biological properties of muscle stem cells. Single myofibers can be cultured in standard plating conditions or in floating conditions. Satellite cells on floating myofibers are subjected to virtually no other influence than the myofiber environment. Substrate stiffness and coating have been shown to influence satellite cells' ability to regenerate muscles 8, 9 so being able to control each of these factors independently allows discrimination between niche-dependent and -independent responses. Different concentrations of serum have also been shown to have an effect on the transition from quiescence to activation. To preserve the quiescence state of its associated satellite cells, fibers should be kept in low serum medium 1-3. This is particularly useful when studying genes involved in the quiescence state. In serum rich medium, satellite cells quickly activate, proliferate, migrate and differentiate, thus mimicking the in vivo regenerative process 1-3. The system can be used to perform a variety of assays such as the testing of chemical inhibitors; ectopic expression of genes by virus delivery; oligonucleotide based gene knock-down or live imaging. This video article describes the protocol currently used in our laboratory to isolate single myofibers from the Extensor Digitorum Longus (EDL) muscle of adult mice (6-8 weeks old).

Isolation and culture of myofibers is the gold standard in vitro system to study the transition of satellite cells through quiescence, activation and differentiation. Importantly, the single myofiber culture system preserves the myofiber/stem cell association, which is an essential component of the muscle stem cell niche.

Muscle  regeneration in the adult is performed by resident stem cells called satellite  cells. Satellite cells are defined by  their position between the ...

Profiling Individual Human Embryonic Stem Cells by Quantitative RT-PCR

Heterogeneity of stem cell population hampers detailed understanding of stem cell biology, such as their differentiation propensity toward different lineages. A single cell transcriptome assay can be a new approach for dissecting individual variation. We have developed the single cell qRT-PCR method, and confirmed that this method works well in several gene expression profiles. In single cell level, each human embryonic stem cell, sorted by OCT4::EGFP positive cells, has high expression in OCT4, but a different level of NANOG expression. Our single cell gene expression assay should be useful to interrogate population heterogeneities.

Single cell gene expression assay is needed for understanding stem cell heterogeneities.

Heterogeneity of stem cell population hampers detailed understanding of stem cell biology, such as their differentiation propensity toward different ...

Strategies for Tracking Anastasis, A Cell Survival Phenomenon that Reverses Apoptosis

Anastasis (Greek for &#8220;rising to life&#8221;) refers to the recovery of dying cells. Before these cells recover, they have passed through important checkpoints of apoptosis, including mitochondrial fragmentation, release of mitochondrial cytochrome c into the cytosol, activation of caspases, chromatin condensation, DNA damage, nuclear fragmentation, plasma membrane blebbing, cell shrinkage, cell surface exposure of phosphatidylserine, and formation of apoptotic bodies. Anastasis can occur when apoptotic stimuli are removed prior to death, thereby allowing dying cells to reverse apoptosis and potentially other death mechanisms. Therefore, anastasis appears to involve physiological healing processes that could also sustain damaged cells inappropriately. The functions and mechanisms of anastasis are still unclear, hampered in part by the limited tools for detecting past events after the recovery of apparently healthy cells. Strategies to detect anastasis will enable studies of the physiological mechanisms, the hazards of undead cells in disease pathology, and potential therapeutics to modulate anastasis. Here, we describe effective strategies using live cell microscopy and a mammalian caspase biosensor&#160;for identifying and tracking anastasis in mammalian cells.

The term anastasis refers to the phenomenon in which dying cells reverse a cell suicide process at a late stage, repair themselves, and ultimately survive. Here we demonstrate protocols for detecting and tracking cells that undergo anastasis.

Anastasis (Greek for &#8220;rising to life&#8221;) refers to the recovery of dying cells. Before these cells recover, they have passed through important ...

Cellular Redox Profiling Using High-content Microscopy

Reactive oxygen species (ROS) regulate essential cellular processes including gene expression, migration, differentiation and proliferation. However, excessive ROS levels induce a state of oxidative stress, which is accompanied by irreversible oxidative damage to DNA, lipids and proteins. Thus, quantification of ROS provides a direct proxy for cellular health condition. Since mitochondria are among the major cellular sources and targets of ROS, joint analysis of mitochondrial function and ROS production in the same cells is crucial for better understanding the interconnection in pathophysiological conditions. Therefore, a high-content microscopy-based strategy was developed for simultaneous quantification of intracellular ROS levels, mitochondrial membrane potential (&#916;&#936;m) and mitochondrial morphology. It is based on automated widefield fluorescence microscopy and image analysis of living adherent cells, grown in multi-well plates, and stained with the cell-permeable fluorescent reporter molecules CM-H2DCFDA (ROS) and TMRM (&#916;&#936;m and mitochondrial morphology). In contrast with fluorimetry or flow-cytometry, this strategy allows quantification of subcellular parameters at the level of the individual cell with high spatiotemporal resolution, both before and after experimental stimulation. Importantly, the image-based nature of the method allows extracting morphological parameters in addition to signal intensities. The combined feature set is used for explorative and statistical multivariate data analysis to detect differences between subpopulations, cell types and/or treatments. Here, a detailed description of the assay is provided, along with an example experiment that proves its potential for unambiguous discrimination between cellular states after chemical perturbation.

This paper presents a high-content microscopy workflow for simultaneous quantification of intracellular ROS levels, as well as mitochondrial membrane potential and morphology &#8211; jointly referred to as mitochondrial morphofunction &#8211; in living adherent cells using the cell-permeant fluorescent reporter molecules 5-(and-6)-chloromethyl-2&#39;,7&#39;-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2DCFDA) and tetramethylrhodamine methylester (TMRM).

Reactive oxygen species (ROS) regulate essential cellular processes including gene expression, migration, differentiation and proliferation. However, ...

TChIP-Seq: Cell-Type-Specific Epigenome Profiling

Epigenetic regulation plays central roles in gene expression. Since histone modification was discovered in the 1960s, its physiological and pathological functions have been extensively studied. Indeed, the advent of next-generation deep sequencing and chromatin immunoprecipitation (ChIP) via specific histone modification antibodies has revolutionized our view of epigenetic regulation across the genome. Conversely, tissues typically consist of diverse cell types, and their complex mixture poses analytic challenges to investigating the epigenome in a particular cell type. To address the cell type-specific chromatin state in a genome-wide manner, we recently developed tandem chromatin immunoprecipitation sequencing (tChIP-Seq), which is based on the selective purification of chromatin by tagged core histone proteins from cell types of interest, followed by ChIP-Seq. The goal of this protocol is the introduction of best practices of tChIP-Seq. This technique provides a versatile tool for tissue-specific epigenome investigation in diverse histone modifications and model organisms.

We describe a step-by-step protocol for tandem chromatin immunoprecipitation sequencing (tChIP-Seq) that enables the analysis of cell-type-specific genome-wide histone modification.

Epigenetic regulation plays central roles in gene expression. Since histone modification was discovered in the 1960s, its physiological and pathological ...