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秀丽隐杆线虫生殖系中的基因转换和末端连接修复双链断裂。

Gene conversion and end-joining-repair double-strand breaks in the Caenorhabditis elegans germline.

作者信息

Robert Valérie J, Davis M Wayne, Jorgensen Erik M, Bessereau Jean-Louis

机构信息

Ecole Normale Supérieure, Biologie Cellulaire de la Synapse, Paris, France.

出版信息

Genetics. 2008 Sep;180(1):673-9. doi: 10.1534/genetics.108.089698. Epub 2008 Aug 30.

DOI:10.1534/genetics.108.089698
PMID:18757928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2535717/
Abstract

Excision of a Mos1 transposon in the germline of Caenorhabditis elegans generates a double-strand break in the chromosome. We demonstrate that breaks are most prominently repaired by gene conversion from the homolog, but also rarely by nonhomologous end-joining. In some cases, gene conversion events are resolved by crossing over. Surprisingly, expression of the transposase using an intestine-specific promoter can induce repair, raising the possibility that activation of transposase expression in somatic cells can lead to transposition of Mos1 in the germline.

摘要

切除秀丽隐杆线虫生殖系中的Mos1转座子会在染色体上产生双链断裂。我们证明,断裂最主要通过同源基因转换进行修复,但也很少通过非同源末端连接进行修复。在某些情况下,基因转换事件通过交叉得以解决。令人惊讶的是,使用肠道特异性启动子表达转座酶可诱导修复,这增加了体细胞中转座酶表达激活可能导致生殖系中Mos1转座的可能性。

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本文引用的文献

1
Environmental RNA interference.环境RNA干扰
Trends Genet. 2008 Jun;24(6):297-305. doi: 10.1016/j.tig.2008.03.007. Epub 2008 Apr 29.
2
C. elegans germ cells switch between distinct modes of double-strand break repair during meiotic prophase progression.秀丽隐杆线虫生殖细胞在减数分裂前期进程中,双链断裂修复的不同模式之间进行转换。
PLoS Genet. 2007 Nov;3(11):e191. doi: 10.1371/journal.pgen.0030191.
3
Gene conversion: mechanisms, evolution and human disease.基因转换:机制、进化与人类疾病
Nat Rev Genet. 2007 Oct;8(10):762-75. doi: 10.1038/nrg2193. Epub 2007 Sep 11.
4
Branching out: meiotic recombination and its regulation.拓展:减数分裂重组及其调控
Trends Cell Biol. 2007 Sep;17(9):448-55. doi: 10.1016/j.tcb.2007.07.007. Epub 2007 Aug 24.
5
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6
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7
Differential usage of non-homologous end-joining and homologous recombination in double strand break repair.双链断裂修复中同源末端连接和同源重组的差异使用
DNA Repair (Amst). 2006 Sep 8;5(9-10):1021-9. doi: 10.1016/j.dnarep.2006.05.022. Epub 2006 Jun 27.
8
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9
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10
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DNA Repair (Amst). 2005 Jun 8;4(6):639-48. doi: 10.1016/j.dnarep.2004.12.005. Epub 2005 Jan 23.