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酵母重组修复基因RAD51的核苷酸序列与转录调控

Nucleotide sequence and transcriptional regulation of the yeast recombinational repair gene RAD51.

作者信息

Basile G, Aker M, Mortimer R K

机构信息

Department of Molecular and Cellular Biology, University of California, Berkeley.

出版信息

Mol Cell Biol. 1992 Jul;12(7):3235-46. doi: 10.1128/mcb.12.7.3235-3246.1992.

DOI:10.1128/mcb.12.7.3235-3246.1992
PMID:1620128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC364538/
Abstract

The RAD51 gene of Saccharomyces cerevisiae is required both for recombination and for the repair of DNA damage caused by X rays. Here we report the sequence and transcriptional regulation of this gene. The RAD51 protein shares significant homology (approximately 50%) over a 70-amino-acid with the RAD57 protein (J.A. Kans and R.K. Mortimer, Gene 105:139-140, 1991), the product of another yeast recombinational repair gene, and also moderate (approximately 27%), but potentially significant, homology with the bacterial RecA protein. The homologies cover a region that encodes a putative nucleotide binding site of the RAD51 protein. Sequences upstream of the coding region for RAD51 protein share homology with the damage response sequence element of RAD54, an upstream activating sequence required for damage regulation of the RAD54 transcript, and also contain two sites for restriction enzyme MluI; the presence of MluI restriction sites has been associated with cell cycle regulation. A 1.6-kb transcript corresponding to RAD51 was observed, and levels of this transcript increased rapidly after exposure to relatively low doses of X-rays. Additionally, RAD51 transcript levels were found to that of a group of genes involved primarily in DNA synthesis and replication which are thought to be coordinately cell cycle regulated. Cells arrested in early G1 were still capable of increasing levels of RAD51 transcript after irradiation, indicating that increased RAD51 transcript levels after X-ray exposure are not solely due to an X-ray-induced cessation of the cell cycle at a period when the level of RAD51 expression is normally high.

摘要

酿酒酵母的RAD51基因对于重组以及修复由X射线引起的DNA损伤都是必需的。在此我们报告该基因的序列和转录调控。RAD51蛋白在一段70个氨基酸的区域内与RAD57蛋白(J.A. 坎斯和R.K. 莫蒂默,《基因》105:139 - 140, 1991)具有显著同源性(约50%),RAD57蛋白是酵母另一个重组修复基因的产物,并且与细菌RecA蛋白也有适度(约27%)但可能显著的同源性。这些同源性覆盖了编码RAD51蛋白一个推定核苷酸结合位点的区域。RAD51蛋白编码区上游的序列与RAD54的损伤反应序列元件具有同源性,RAD54的损伤反应序列元件是RAD54转录本损伤调控所需的上游激活序列,并且还包含两个限制性内切酶MluI的位点;MluI限制性位点的存在与细胞周期调控有关。观察到一个与RAD51相对应的1.6 kb转录本,并且在暴露于相对低剂量的X射线后,该转录本的水平迅速增加。此外,发现RAD51转录本水平与一组主要参与DNA合成和复制的基因的转录本水平相关,这些基因被认为是受细胞周期协调调控的。停滞在G1早期的细胞在照射后仍能够增加RAD51转录本的水平,这表明X射线暴露后RAD51转录本水平的增加并非仅仅是由于X射线诱导细胞周期在RAD51表达水平通常较高的时期停止。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/871d007e0028/molcellb00029-0346-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/2e2a14cfd0b3/molcellb00029-0344-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/d6658a644b12/molcellb00029-0345-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/67a2cf10e6e3/molcellb00029-0345-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/593e3e542955/molcellb00029-0346-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/871d007e0028/molcellb00029-0346-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/2e2a14cfd0b3/molcellb00029-0344-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/d6658a644b12/molcellb00029-0345-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/67a2cf10e6e3/molcellb00029-0345-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/593e3e542955/molcellb00029-0346-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/054c/364538/871d007e0028/molcellb00029-0346-b.jpg

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