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pubmed-article:21501635pubmed:abstractTextRAD51 and RAD54, members of the RAD52 epistasis group, play key roles in homologous recombination (HR). The efficiency of homologous recombination (HR) can be increased by over-expression of either of them. A vector that allows co-expression of RAD51 and RAD54 was constructed to investigate interactions between the two proteins during extra-chromosomal HR. The efficiency of extra-chromosomal HR evaluated by GFP extra-chromosomal HR was enhanced (110-245%) in different transfected Human sarcoma (HT-1080) cell colonies. We observed that RAD51 clearly promotes extra-chromosomal HR; however, the actions of RAD54 in extra-chromosomal HR were weak. Our data suggest that RAD51 may function as a universal factor during HR, whereas RAD54 mainly functions in other types of HR (gene targeting or intra-chromosomal HR), which involves interaction with chromosomal DNA.lld:pubmed
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pubmed-article:21501635pubmed:authorpubmed-author:YuShengliSlld:pubmed
pubmed-article:21501635pubmed:copyrightInfoPublished by Elsevier B.V.lld:pubmed
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pubmed-article:21501635pubmed:articleTitleOver-expression of RAD51 or RAD54 but not RAD51/4 enhances extra-chromosomal homologous recombination in the human sarcoma (HT-1080) cell line.lld:pubmed
pubmed-article:21501635pubmed:affiliationState Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing, People's Republic of China. victory811111@126.comlld:pubmed
pubmed-article:21501635pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21501635pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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