JoVE Logo

Zaloguj się

7.16 : Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.

The recognition sites for Cre recombinase called LoxP sites are around 34 basepairs in length. LoxP sites contain 13 bp palindromic sequences, meaning that the nucleotide sequence reads the same in both 5’ to 3’ and 3’ to 5’ directions. Site-specific recombination mediated by Cre recombinases is one of the most popular methods used in the creation of transgenic mice with acquired mutations. Using thermostable variants of Cre recombinase with tissue specific promoters allows for spatial control over Cre recombinase's expression and action. For instance, placing a kidney-specific Cadherin promoter upstream of the Cre gene allows the enzyme to be expressed only in renal tissues. For temporal control of Cre recombinase activity, the enzyme gene is fused with a ligand binding domain so that the enzyme is expressed only in the specific ligand’s presence.

A major limitation in using site-specific recombination as a genome editing tool is that the recombination target site or sites must be first inserted or must be present by chance. If a genomic site congruent with the enzyme recognition site can be preselected, the recombinases can be used with “made-to-order” target specificity. Recent studies have used mutagenesis and gene shuffling to design Flp variants that can functionally recognize sites with combinatorial mutations. The results are promising for future iterations of gene shuffling that can yield more specific Flp variants and can be used commercially as a molecular tool for engineering large genomes.

Tagi

Conservative Site specific RecombinationPhase VariationGenetic ExchangeSite specific RecombinasesDNA SectionsSequence HomologySymmetric SequencesSerine RecombinaseTyrosine RecombinaseEnzyme MechanismsSynaptic ComplexCrossover SitesStrand ExchangeCovalent BondingHolliday Junction IntermediateCleaved DNA Strands

Z rozdziału 7:

article

Now Playing

7.16 : Conservative Site-specific Recombination and Phase Variation

DNA Repair and Recombination

5.9K Wyświetleń

article

7.1 : Przegląd naprawy DNA

DNA Repair and Recombination

29.7K Wyświetleń

article

7.2 : Naprawa wycięcia podstawy

DNA Repair and Recombination

21.8K Wyświetleń

article

7.3 : Naprawa wycięcia podstawy z długą łatą

DNA Repair and Recombination

6.9K Wyświetleń

article

7.4 : Naprawa przez wycinanie nukleotydów

DNA Repair and Recombination

11.1K Wyświetleń

article

7.5 : Translezja DNA Polimerazy

DNA Repair and Recombination

9.7K Wyświetleń

article

7.6 : Naprawianie pęknięć dwużyłowych

DNA Repair and Recombination

11.9K Wyświetleń

article

7.7 : Uszkodzenie DNA może zatrzymać cykl komórkowy

DNA Repair and Recombination

9.0K Wyświetleń

article

7.8 : Rekombinacja homologiczna

DNA Repair and Recombination

49.9K Wyświetleń

article

7.9 : Ponowne uruchamianie zablokowanych widełek replikacji

DNA Repair and Recombination

5.7K Wyświetleń

article

7.10 : Konwersja genów

DNA Repair and Recombination

9.6K Wyświetleń

article

7.11 : Przegląd transpozycji i rekombinacji

DNA Repair and Recombination

15.1K Wyświetleń

article

7.12 : Transpozony tylko DNA

DNA Repair and Recombination

14.3K Wyświetleń

article

7.13 : Retrowirusy

DNA Repair and Recombination

12.1K Wyświetleń

article

7.14 : Retrotranspozony LTR

DNA Repair and Recombination

17.3K Wyświetleń

See More

JoVE Logo

Prywatność

Warunki Korzystania

Zasady

Badania

Edukacja

O JoVE

Copyright © 2025 MyJoVE Corporation. Wszelkie prawa zastrzeżone