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1
The fate of 8-methoxypsoralen photoinduced crosslinks in nuclear and mitochondrial yeast DNA: comparison of wild-type and repair-deficient strains.8-甲氧基补骨脂素光诱导交联在酵母细胞核和线粒体DNA中的命运:野生型和修复缺陷型菌株的比较。
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1722-6. doi: 10.1073/pnas.79.6.1722.
2
S. cerevisiae has three pathways for DNA interstrand crosslink repair.酿酒酵母具有三条DNA链间交联修复途径。
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3
Preferential repair in Saccharomyces cerevisiae rad mutants after induction of interstrand cross-links by 8-methoxypsoralen plus UVA.在8-甲氧基补骨脂素加紫外线A诱导链间交联后,酿酒酵母rad突变体中的优先修复。
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4
Repair of 8-methoxypsoralen photoinduced cross-links in yeast. Analysis by alkaline step-elution and electron microscopy.酵母中8-甲氧基补骨脂素光诱导交联的修复。通过碱性逐步洗脱和电子显微镜分析。
Mol Gen Genet. 1991 Sep;228(3):335-44. doi: 10.1007/BF00260625.
5
Genetic control of the bypass of mono-adducts and of the repair of cross-links photoinduced by 8-methoxypsoralen in yeast.酵母中8-甲氧基补骨脂素光诱导的单加合物旁路和交联修复的遗传控制。
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Further characterization of the role of Pso2 in the repair of DNA interstrand cross-link-associated double-strand breaks in Saccharomyces cerevisiae.酿酒酵母中Pso2在DNA链间交联相关双链断裂修复中作用的进一步表征。
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A rapid method to monitor repair and mis-repair of DNA double-strand breaks by using cell extracts of the yeast Saccharomyces cerevisiae.一种利用酿酒酵母细胞提取物监测DNA双链断裂修复和错配修复的快速方法。
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Mol Gen Genet. 1984;193(1):167-71. doi: 10.1007/BF00327432.
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Repair of MMS-induced DNA double-strand breaks in haploid cells of Saccharomyces cerevisiae, which requires the presence of a duplicate genome.酿酒酵母单倍体细胞中MMS诱导的DNA双链断裂的修复,这需要存在一个重复的基因组。
Mol Gen Genet. 1979 Jan 2;167(3):279-86. doi: 10.1007/BF00267420.

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本文引用的文献

1
DNA repair in human cells containing photoadducts of 8-methoxypsoralen or angelicin.含有8-甲氧基补骨脂素或当归素光加合物的人类细胞中的DNA修复
Cancer Res. 1980 Mar;40(3):696-702.
2
Repair of interstrand cross-links in DNA of Saccharomyces cerevisiae requires two systems for DNA repair: the RAD3 system and the RAD51 system.酿酒酵母DNA中链间交联的修复需要两个DNA修复系统:RAD3系统和RAD51系统。
Mol Gen Genet. 1981;182(2):196-205. doi: 10.1007/BF00269658.
3
Repair of DNA double-strand breaks in Escherichia coli cells requires synthesis of proteins that can be induced by UV light.大肠杆菌细胞中DNA双链断裂的修复需要合成可被紫外线诱导的蛋白质。
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3450-3. doi: 10.1073/pnas.78.6.3450.
4
The effects of three PSO genes on induced mutagenesis : a novel class of mutationally defective yeast.三个PSO基因对诱导诱变的影响:一类新型的突变缺陷型酵母。
Genetics. 1980 Dec;96(4):841-57. doi: 10.1093/genetics/96.4.841.
5
Isolation and characterization of pso mutants sensitive to photo-addition of psoralen derivatives in Saccharomyces cerevisiae.酿酒酵母中对补骨脂素衍生物光加成敏感的pso突变体的分离与鉴定
Genetics. 1980 Jun;95(2):273-88. doi: 10.1093/genetics/95.2.273.
6
Genetic control of diploid recovery after gamma-irradiation in the yeast Saccharomyces cerevisiae.酿酒酵母经γ射线辐照后二倍体恢复的遗传控制。
Mutat Res. 1980 Dec;73(2):251-65. doi: 10.1016/0027-5107(80)90192-x.
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Psoralen photochemistry.
Photochem Photobiol. 1980 Dec;32(6):813-21. doi: 10.1111/j.1751-1097.1980.tb04061.x.
8
The role of dimer excision in liquid-holding recovery of UV-irradiated haploid yeast.
Mutat Res. 1980 Jan;69(1):19-41. doi: 10.1016/0027-5107(80)90173-6.
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[Absence of interstrand cross-links in DNA treated wtih 3-carbethoxypsoralen and 365 nm irradiation].
C R Seances Acad Sci D. 1980 Sep 15;291(2):207-10.
10
Discontinuities in the DNA synthesized in an excision-defective strain of Escherichia coli following ultraviolet irradiation.紫外线照射后,大肠杆菌切除缺陷菌株中合成的DNA的不连续性。
J Mol Biol. 1968 Jan 28;31(2):291-304. doi: 10.1016/0022-2836(68)90445-2.

8-甲氧基补骨脂素光诱导交联在酵母细胞核和线粒体DNA中的命运:野生型和修复缺陷型菌株的比较。

The fate of 8-methoxypsoralen photoinduced crosslinks in nuclear and mitochondrial yeast DNA: comparison of wild-type and repair-deficient strains.

作者信息

Magaña-Schwencke N, Henriques J A, Chanet R, Moustacchi E

出版信息

Proc Natl Acad Sci U S A. 1982 Mar;79(6):1722-6. doi: 10.1073/pnas.79.6.1722.

DOI:10.1073/pnas.79.6.1722
PMID:6281782
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC346052/
Abstract

In Saccharomyces cerevisiae, after 8-methoxypsoralen [8-(OMe)Ps] photoaddition, more crosslinks are induced per unit dose in mitochondrial DNA than in nuclear DNA. In wild-type cells treated in the exponential phase of growth, single- and double-strand breaks are produced during crosslink removal and then are rejoined upon postexposure incubation. The incision step is almost blocked in the rad 3-2 mutant, which is also defective in excision-repair of UV-induced (254 nm) pyrimidine dimers. The cutting of crosslinks from nuclear DNA is depressed in wild-type stationary-phase cells. This is correlated with a higher sensitivity of such cells to 8-(OMe)Ps photoinduced cell killing. The incision of crosslinks is dramatically reduced in mitochondrial DNA. The rejoining of single- and double-strand breaks is not only dependent on the product of the RAD51 gene (as shown by others) but also of the PSO2 gene. A correlation was found between the ability to recombine and strand rejoining. Therefore, as in bacteria, both the excision and the recombinational repair systems are involved in crosslink repair in yeast. However, double-strand breaks in yeast constitute repair intermediates which are not detected in Escherichia coli. The LD37 (dose necessary to induce a mean of one lethal hit per cell) corresponds to about 120 crosslinks per genome in exponential-phase cells of the wild type and to 1-2 crosslinks in the pso2-1 mutant.

摘要

在酿酒酵母中,8-甲氧基补骨脂素[8-(OMe)Ps]光加成后,线粒体DNA中每单位剂量诱导产生的交联比核DNA更多。在指数生长期处理的野生型细胞中,交联去除过程中会产生单链和双链断裂,然后在暴露后孵育时重新连接。在rad 3-2突变体中,切口步骤几乎被阻断,该突变体在紫外线诱导(254 nm)嘧啶二聚体的切除修复方面也存在缺陷。野生型静止期细胞中核DNA交联的切割受到抑制。这与此类细胞对8-(OMe)Ps光诱导细胞杀伤的更高敏感性相关。线粒体DNA中交联的切口显著减少。单链和双链断裂的重新连接不仅依赖于RAD51基因的产物(如其他人所示),还依赖于PSO2基因。发现重组能力与链重新连接之间存在相关性。因此,与细菌一样,切除和重组修复系统都参与了酵母中的交联修复。然而,酵母中的双链断裂构成了修复中间体,这在大肠杆菌中未被检测到。野生型指数期细胞的LD37(每细胞平均诱导一次致死性损伤所需的剂量)对应于每个基因组约120个交联,而在pso2-1突变体中为1-2个交联。