Recombineering: Difference between revisions

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http://recombineering.ncifcrf.gov/
http://web.ncifcrf.gov/research/brb/recombineeringInformation.aspx




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This process is then adapted to E-coli strain DH10B, a Bacteria Artificial Chromosome (BAC)strain. This results in the original recombineering E-coli strain designated DY380 as well as other versions modified to include different selection mechanisms.
This process is then adapted to E-coli strain DH10B, a Bacteria Artificial Chromosome (BAC)strain. This results in the original recombineering E-coli strain designated DY380 as well as other versions modified to include different selection mechanisms.
[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11352566 Lee 2001. A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA]
[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11352566 Lee 2001. A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA]
For additional information on protocols, strains, and recombineering agents being developed by the Court lab at NCI-Frederick please check their website: http://redrecombineering.ncifcrf.gov/





Latest revision as of 09:56, 1 February 2012

Protocols

Resources

Recombineering is a method where E-coli undergoes recombination between linear DNA, introduced through electroporation, with circularized DNA already present within the cell.


http://web.ncifcrf.gov/research/brb/recombineeringInformation.aspx


[math]\displaystyle{ \lambda }[/math] phage exo, bet, and gam genes are integrated into E-coli to demonstrate phage promoted homologous recombination. Murphy 1998 [math]\displaystyle{ \lambda }[/math] Red-Promoted Gene Replacement


To acheive control over phage recombination gene activity, temperature sensitive [math]\displaystyle{ \lambda }[/math] repressor (cI857) was introduced. Yu 2000 An efficient recombination system for chromosome engineering in Escherichia coli


Court Lab.

This process is then adapted to E-coli strain DH10B, a Bacteria Artificial Chromosome (BAC)strain. This results in the original recombineering E-coli strain designated DY380 as well as other versions modified to include different selection mechanisms. Lee 2001. A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

For additional information on protocols, strains, and recombineering agents being developed by the Court lab at NCI-Frederick please check their website: http://redrecombineering.ncifcrf.gov/


Church Lab.

Methods for generating precise deletions and insertions in the genome of wild-type Escherichia coli: application to open reading frame characterization-



All about the [math]\displaystyle{ \lambda }[/math] phage recombination proteins, exonuclease, [math]\displaystyle{ \beta }[/math], and [math]\displaystyle{ \gamma }[/math]!!


An Exonuclease Induced by phage [math]\displaystyle{ \lambda }[/math]. Little 1967

Roles of Exonuclease and [math]\displaystyle{ \beta }[/math] protein of phage [math]\displaystyle{ \lambda }[/math] in recombination. Carter 1971


[math]\displaystyle{ \beta }[/math] protein of phage [math]\displaystyle{ \lambda }[/math] promotes renaturation of DNA. Kmiec 1981

Pairing activities of [math]\displaystyle{ \beta }[/math] protein in phage [math]\displaystyle{ \lambda }[/math]. Muniyappa 1986


How [math]\displaystyle{ \gamma }[/math] protein specified by phage [math]\displaystyle{ \lambda }[/math] affects recBC enzyme in E. Coli. Karu 1975

[math]\displaystyle{ \gamma }[/math] protein of phage [math]\displaystyle{ \lambda }[/math] inhibits recombination activites of RecBCD enzyme. Murphy 1991