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重组蛋白参与紫外线照射的大肠杆菌中停滞复制叉的挽救过程不一定涉及重组。

Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination.

作者信息

Courcelle J, Hanawalt P C

机构信息

Department of Biological Sciences, Mississippi State University, P.O. Box GY, Mississippi State, MS 39762-5759, USA.

出版信息

Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8196-202. doi: 10.1073/pnas.121008898.

DOI:10.1073/pnas.121008898
PMID:11459953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC37421/
Abstract

Alternative reproductive cycles make use of different strategies to generate different reproductive products. In Escherichia coli, recA and several other rec genes are required for the generation of recombinant genomes during Hfr conjugation. During normal asexual reproduction, many of these same genes are needed to generate clonal products from UV-irradiated cells. However, unlike conjugation, this latter process also requires the function of the nucleotide excision repair genes. Following UV irradiation, the recovery of DNA replication requires uvrA and uvrC, as well as recA, recF, and recR. The rec genes appear to be required to protect and maintain replication forks that are arrested at DNA lesions, based on the extensive degradation of the nascent DNA that occurs in their absence. The products of the recJ and recQ genes process the blocked replication forks before the resumption of replication and may affect the fidelity of the recovery process. We discuss a model in which several rec gene products process replication forks arrested by DNA damage to facilitate the repair of the blocking DNA lesions by nucleotide excision repair, thereby allowing processive replication to resume with no need for strand exchanges or recombination. The poor survival of cellular populations that depend on recombinational pathways (compared with that in their excision repair proficient counterparts) suggests that at least some of the rec genes may be designed to function together with nucleotide excision repair in a common and predominant pathway by which cells faithfully recover replication and survive following UV-induced DNA damage.

摘要

交替的生殖周期利用不同策略来产生不同的生殖产物。在大肠杆菌中,Hfr 接合过程中产生重组基因组需要 recA 和其他几个 rec 基因。在正常的无性繁殖过程中,从紫外线照射的细胞产生克隆产物也需要许多相同的基因。然而,与接合不同的是,后一过程还需要核苷酸切除修复基因的功能。紫外线照射后,DNA 复制的恢复需要 uvrA、uvrC 以及 recA、recF 和 recR。基于在缺乏 rec 基因时新生 DNA 会发生广泛降解这一情况,rec 基因似乎是保护和维持停滞在 DNA 损伤处的复制叉所必需的。recJ 和 recQ 基因的产物在复制恢复之前处理受阻的复制叉,并且可能影响恢复过程的保真度。我们讨论了一个模型,其中几种 rec 基因产物处理因 DNA 损伤而停滞的复制叉,以促进通过核苷酸切除修复来修复阻断性 DNA 损伤,从而使连续复制能够恢复,而无需进行链交换或重组。依赖重组途径的细胞群体的低存活率(与切除修复能力强的对应群体相比)表明,至少一些 rec 基因可能被设计为与核苷酸切除修复一起在一个共同且主要的途径中发挥作用,通过该途径细胞在紫外线诱导的 DNA 损伤后能够忠实地恢复复制并存活。

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本文引用的文献

1
ISOLATION AND CHARACTERIZATION OF RECOMBINATION-DEFICIENT MUTANTS OF ESCHERICHIA COLI K12.大肠杆菌K12重组缺陷突变体的分离与鉴定
Proc Natl Acad Sci U S A. 1965 Feb;53(2):451-9. doi: 10.1073/pnas.53.2.451.
2
THYMINE DIMERS AND INHIBITION OF DNA SYNTHESIS BY ULTRAVIOLET IRRADIATION OF CELLS.胸腺嘧啶二聚体与紫外线照射细胞对DNA合成的抑制作用
Science. 1963 Dec 13;142(3598):1464-6. doi: 10.1126/science.142.3598.1464.
3
Sex in bacteria; genetic studies, 1945-1952.
Science. 1953 Aug 14;118(3059):169-75. doi: 10.1126/science.118.3059.169.
4
Therefore, what are recombination proteins there for?那么,重组蛋白的作用是什么呢?
Bioessays. 2001 May;23(5):463-70. doi: 10.1002/bies.1065.
5
Comparative gene expression profiles following UV exposure in wild-type and SOS-deficient Escherichia coli.野生型和SOS缺陷型大肠杆菌紫外线照射后的基因表达谱比较
Genetics. 2001 May;158(1):41-64. doi: 10.1093/genetics/158.1.41.
6
PriA-directed replication fork restart in Escherichia coli.大肠杆菌中PriA引导的复制叉重启
Trends Biochem Sci. 2000 Apr;25(4):185-9. doi: 10.1016/s0968-0004(00)01565-6.
7
The importance of repairing stalled replication forks.修复停滞的复制叉的重要性。
Nature. 2000 Mar 2;404(6773):37-41. doi: 10.1038/35003501.
8
RecQ family helicases: roles in cancer and aging.RecQ家族解旋酶:在癌症和衰老中的作用。
Curr Opin Genet Dev. 2000 Feb;10(1):32-8. doi: 10.1016/s0959-437x(99)00039-8.
9
RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli.在紫外线照射的大肠杆菌中,RecQ和RecJ在复制重新开始之前处理受阻的复制叉。
Mol Gen Genet. 1999 Oct;262(3):543-51. doi: 10.1007/s004380051116.
10
Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.大肠杆菌和噬菌体λ中DNA损伤的重组修复
Microbiol Mol Biol Rev. 1999 Dec;63(4):751-813, table of contents. doi: 10.1128/MMBR.63.4.751-813.1999.