Literature DB >> 14769965

Chromatin immunoprecipitation to investigate protein-DNA interactions during genetic recombination.

Tamara Goldfarb1, Eric Alani.   

Abstract

Chromatin immunoprecipitation is a technique that allows one to examine the in vivo localization of proteins to DNA. This technique is well suited for studying genetic recombination since it can provide both a temporal and spatial assessment of the dynamic association of proteins with DNA in both wild-type and mutant backgrounds. To perform this procedure, cells undergoing a synchronous recombination event are treated with a crosslinking agent. Following cell lysis and shearing of the DNA, immunoprecipitation is used to isolate the protein of interest, along with any DNA that is crosslinked to the protein. Polymerase chain reaction (PCR) is then used to determine the relative amounts of DNA associated with the protein of interest throughout the recombination event. This in vivo chemical crosslinking technique can be used to localize proteins to both double-strand breaks and recombination intermediates.

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Year:  2004        PMID: 14769965     DOI: 10.1385/1-59259-761-0:223

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  Mcm10 mediates the interaction between DNA replication and silencing machineries.

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Journal:  Genetics       Date:  2008-12-08       Impact factor: 4.562

2.  Tethering recombination initiation proteins in Saccharomyces cerevisiae promotes double strand break formation.

Authors:  Demelza R Koehn; Stuart J Haring; Jaime M Williams; Robert E Malone
Journal:  Genetics       Date:  2009-03-30       Impact factor: 4.562

3.  Mutants defective in Rad1-Rad10-Slx4 exhibit a unique pattern of viability during mating-type switching in Saccharomyces cerevisiae.

Authors:  Amy M Lyndaker; Tamara Goldfarb; Eric Alani
Journal:  Genetics       Date:  2008-06-24       Impact factor: 4.562

4.  Phosphoinositide [PI(3,5)P2] lipid-dependent regulation of the general transcriptional regulator Tup1.

Authors:  Bong-Kwan Han; Scott D Emr
Journal:  Genes Dev       Date:  2011-05-01       Impact factor: 11.361

5.  Distinct requirements within the Msh3 nucleotide binding pocket for mismatch and double-strand break repair.

Authors:  Charanya Kumar; Gregory M Williams; Brett Havens; Michelle K Dinicola; Jennifer A Surtees
Journal:  J Mol Biol       Date:  2013-02-28       Impact factor: 5.469

Review 6.  A tale of tails: insights into the coordination of 3' end processing during homologous recombination.

Authors:  Amy M Lyndaker; Eric Alani
Journal:  Bioessays       Date:  2009-03       Impact factor: 4.345

7.  The phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2)-dependent Tup1 conversion (PIPTC) regulates metabolic reprogramming from glycolysis to gluconeogenesis.

Authors:  Bong-Kwan Han; Scott D Emr
Journal:  J Biol Chem       Date:  2013-06-03       Impact factor: 5.157

  7 in total

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