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1
The Drosophila meiotic recombination gene mei-9 encodes a homologue of the yeast excision repair protein Rad1.果蝇减数分裂重组基因mei-9编码酵母切除修复蛋白Rad1的同源物。
Genetics. 1995 Oct;141(2):619-27. doi: 10.1093/genetics/141.2.619.
2
Positional cloning of the Drosophila melanogaster mei-9 gene, the putative homolog of the Saccharomyces cerevisiae RAD1 gene.黑腹果蝇mei-9基因的定位克隆,该基因被认为是酿酒酵母RAD1基因的同源基因。
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3
ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.ERCC4(XPF)编码一种具有真核生物重组同源物的人类核苷酸切除修复蛋白。
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Nucleotide excision repair endonuclease genes in Drosophila melanogaster.黑腹果蝇中的核苷酸切除修复内切核酸酶基因。
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mei-W68 in Drosophila melanogaster encodes a Spo11 homolog: evidence that the mechanism for initiating meiotic recombination is conserved.黑腹果蝇中的mei-W68编码一种Spo11同源物:启动减数分裂重组的机制具有保守性的证据。
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Characterization of the roles of the Saccharomyces cerevisiae RAD54 gene and a homologue of RAD54, RDH54/TID1, in mitosis and meiosis.酿酒酵母RAD54基因及RAD54同源物RDH54/TID1在有丝分裂和减数分裂中的作用表征。
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Yeast DNA recombination and repair proteins Rad1 and Rad10 constitute a complex in vivo mediated by localized hydrophobic domains.酵母DNA重组与修复蛋白Rad1和Rad10在体内由局部疏水结构域介导形成一个复合体。
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8
RAD1 and RAD10, but not other excision repair genes, are required for double-strand break-induced recombination in Saccharomyces cerevisiae.酿酒酵母中,双链断裂诱导的重组需要RAD1和RAD10基因,但不需要其他切除修复基因。
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MUS81 encodes a novel helix-hairpin-helix protein involved in the response to UV- and methylation-induced DNA damage in Saccharomyces cerevisiae.MUS81编码一种新型的螺旋-发夹-螺旋蛋白,该蛋白参与酿酒酵母对紫外线和甲基化诱导的DNA损伤的反应。
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Genetic evidence for different RAD52-dependent intrachromosomal recombination pathways in Saccharomyces cerevisiae.酿酒酵母中不同的RAD52依赖性染色体内重组途径的遗传证据。
Curr Genet. 1995 Mar;27(4):298-305. doi: 10.1007/BF00352096.

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The XPF-ERCC1 Complex Is Essential for Genome Stability and Is Involved in the Mechanism of Gene Targeting in .XPF-ERCC1复合物对基因组稳定性至关重要,并参与了……中的基因靶向机制。
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Meiotic MCM Proteins Promote and Inhibit Crossovers During Meiotic Recombination.减数分裂期 MCM 蛋白在减数分裂重组过程中促进和抑制交叉。
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Molecular Evolution at a Meiosis Gene Mediates Species Differences in the Rate and Patterning of Recombination.分子进化在减数分裂基因中介导了物种间重组率和模式的差异。
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本文引用的文献

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The Role of Radiation (rad) Genes in Meiotic Recombination in Yeast.辐射(rad)基因在酵母减数分裂重组中的作用。
Genetics. 1980 Jan;94(1):51-68. doi: 10.1093/genetics/94.1.51.
2
Effects of the RAD52 Gene on Recombination in SACCHAROMYCES CEREVISIAE.RAD52 基因对酿酒酵母重组的影响。
Genetics. 1980 Jan;94(1):31-50. doi: 10.1093/genetics/94.1.31.
3
The Utilization during Mitotic Cell Division of Loci Controlling Meiotic Recombination and Disjunction in DROSOPHILA MELANOGASTER.有丝分裂细胞分裂过程中控制减数分裂重组和分离的位点在黑腹果蝇中的利用。
Genetics. 1978 Nov;90(3):531-78. doi: 10.1093/genetics/90.3.531.
4
Yeast DNA repair and recombination proteins Rad1 and Rad10 constitute a single-stranded-DNA endonuclease.酵母DNA修复和重组蛋白Rad1和Rad10构成一种单链DNA内切核酸酶。
Nature. 1993 Apr 29;362(6423):860-2. doi: 10.1038/362860a0.
5
Physical detection of heteroduplexes during meiotic recombination in the yeast Saccharomyces cerevisiae.酿酒酵母减数分裂重组过程中异源双链体的物理检测。
Mol Cell Biol. 1993 Apr;13(4):2324-31. doi: 10.1128/mcb.13.4.2324-2331.1993.
6
Timing of molecular events in meiosis in Saccharomyces cerevisiae: stable heteroduplex DNA is formed late in meiotic prophase.酿酒酵母减数分裂中分子事件的时间安排:稳定的异源双链DNA在减数分裂前期后期形成。
Mol Cell Biol. 1993 Jan;13(1):373-82. doi: 10.1128/mcb.13.1.373-382.1993.
7
Identification of joint molecules that form frequently between homologs but rarely between sister chromatids during yeast meiosis.鉴定在酵母减数分裂过程中同源染色体之间频繁形成但姐妹染色单体之间很少形成的联合分子。
Cell. 1994 Jan 14;76(1):51-63. doi: 10.1016/0092-8674(94)90172-4.
8
It was a very good year for DNA repair.对DNA修复来说,这是非常不错的一年。
Cell. 1994 Jan 14;76(1):1-4. doi: 10.1016/0092-8674(94)90165-1.
9
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.一种涉及ERCC1以及ERCC4、ERCC11和着色性干皮病F组互补活性的修复酶复合物的证据。
EMBO J. 1993 Sep;12(9):3693-701. doi: 10.1002/j.1460-2075.1993.tb06044.x.
10
Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.体外共校正ERCC1、ERCC4和着色性干皮病F组的DNA修复缺陷。
EMBO J. 1993 Sep;12(9):3685-92. doi: 10.1002/j.1460-2075.1993.tb06043.x.

果蝇减数分裂重组基因mei-9编码酵母切除修复蛋白Rad1的同源物。

The Drosophila meiotic recombination gene mei-9 encodes a homologue of the yeast excision repair protein Rad1.

作者信息

Sekelsky J J, McKim K S, Chin G M, Hawley R S

机构信息

Section of Molecular and Cellular Biology, University of California, Davis 95616, USA.

出版信息

Genetics. 1995 Oct;141(2):619-27. doi: 10.1093/genetics/141.2.619.

DOI:10.1093/genetics/141.2.619
PMID:8647398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1206761/
Abstract

Meiotic recombination and DNA repair are mediated by overlapping sets of genes. In the yeast Saccharomyces cerevisiae, many genes required to repair DNA double-strand breaks are also required for meiotic recombination. In contrast, mutations in genes required for nucleotide excision repair (NER) have no detectable effects on meiotic recombination in S. cerevisiae. The Drosophila melanogaster mei-9 gene is unique among known recombination genes in that it is required for both meiotic recombination and NER. We have analyzed the mei-9 gene at the molecular level and found that it encodes a homologue of the S. cerevisiae excision repair protein Rad1, the probable homologue of mammalian XPF/ERCC4. Hence, the predominant process of meiotic recombination in Drosophila proceeds through a pathway that is at least partially distinct from that of S. cerevisiae, in that it requires an NER protein. The biochemical properties of the Rad1 protein allow us to explain the observation that mei-9 mutants suppress reciprocal exchange without suppressing the frequency of gene conversion.

摘要

减数分裂重组和DNA修复由重叠的基因集介导。在酿酒酵母中,修复DNA双链断裂所需的许多基因也是减数分裂重组所必需的。相比之下,核苷酸切除修复(NER)所需基因的突变对酿酒酵母的减数分裂重组没有可检测到的影响。黑腹果蝇的mei-9基因在已知的重组基因中是独特的,因为它对于减数分裂重组和NER都是必需的。我们已经在分子水平上分析了mei-9基因,发现它编码酿酒酵母切除修复蛋白Rad1的同源物,可能是哺乳动物XPF/ERCC4的同源物。因此,果蝇减数分裂重组的主要过程通过至少部分不同于酿酒酵母的途径进行,因为它需要一种NER蛋白。Rad1蛋白的生化特性使我们能够解释mei-9突变体抑制相互交换而不抑制基因转换频率的观察结果。