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1
Genetic control of RNA polymerase I-stimulated recombination in yeast.酵母中RNA聚合酶I刺激的重组的遗传控制
Genetics. 1990 Sep;126(1):41-52. doi: 10.1093/genetics/126.1.41.
2
Mutations affecting RNA polymerase I-stimulated exchange and rDNA recombination in yeast.影响酵母中RNA聚合酶I刺激的交换和核糖体DNA重组的突变。
Genetics. 1991 Jan;127(1):31-8. doi: 10.1093/genetics/127.1.31.
3
RAD1, an excision repair gene of Saccharomyces cerevisiae, is also involved in recombination.RAD1是酿酒酵母的一种切除修复基因,它也参与重组过程。
Mol Cell Biol. 1988 Sep;8(9):3619-26. doi: 10.1128/mcb.8.9.3619-3626.1988.
4
A chromosome containing HOT1 preferentially receives information during mitotic interchromosomal gene conversion.含有HOT1的染色体在有丝分裂染色体间基因转换过程中优先接收信息。
Genetics. 1990 Mar;124(3):561-72. doi: 10.1093/genetics/124.3.561.
5
DEG1, encoding the tRNA:pseudouridine synthase Pus3p, impacts HOT1-stimulated recombination in Saccharomyces cerevisiae.编码tRNA:假尿苷合酶Pus3p的DEG1,影响酿酒酵母中HOT1刺激的重组。
Mol Genet Genomics. 2005 Dec;274(5):528-38. doi: 10.1007/s00438-005-0042-3. Epub 2005 Oct 18.
6
The genetic control of direct-repeat recombination in Saccharomyces: the effect of rad52 and rad1 on mitotic recombination at GAL10, a transcriptionally regulated gene.酿酒酵母中直接重复序列重组的遗传控制:rad52和rad1对转录调控基因GAL10处有丝分裂重组的影响。
Genetics. 1989 Dec;123(4):725-38. doi: 10.1093/genetics/123.4.725.
7
Requirements for activity of the yeast mitotic recombination hotspot HOT1: RNA polymerase I and multiple cis-acting sequences.酵母有丝分裂重组热点HOT1活性的要求:RNA聚合酶I和多个顺式作用序列。
Genetics. 1995 Nov;141(3):845-55. doi: 10.1093/genetics/141.3.845.
8
Gene conversion tracts stimulated by HOT1-promoted transcription are long and continuous.由HOT1促进转录所刺激的基因转换片段长且连续。
Genetics. 1990 Dec;126(4):851-67. doi: 10.1093/genetics/126.4.851.
9
Transcription by RNA polymerase I stimulates mitotic recombination in Saccharomyces cerevisiae.RNA聚合酶I的转录会刺激酿酒酵母中的有丝分裂重组。
Mol Cell Biol. 1989 Aug;9(8):3464-72. doi: 10.1128/mcb.9.8.3464-3472.1989.
10
RAD10, an excision repair gene of Saccharomyces cerevisiae, is involved in the RAD1 pathway of mitotic recombination.RAD10是酿酒酵母的一种切除修复基因,参与有丝分裂重组的RAD1途径。
Mol Cell Biol. 1990 Jun;10(6):2485-91. doi: 10.1128/mcb.10.6.2485-2491.1990.

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Genes Dev. 2015 Jun 1;29(11):1188-201. doi: 10.1101/gad.260844.115.
2
Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery.在芽殖酵母核糖体 DNA 中,重复扩展可以独立于规范的同源重组机制发生。
Nucleic Acids Res. 2011 Nov 1;39(20):8778-91. doi: 10.1093/nar/gkr589. Epub 2011 Jul 17.
3
Contrasting roles of checkpoint proteins as recombination modulators at Fob1-Ter complexes with or without fork arrest.在有或没有叉形停滞的Fob1-Ter复合物中,检查点蛋白作为重组调节剂的对比作用。
Eukaryot Cell. 2009 Apr;8(4):487-95. doi: 10.1128/EC.00382-08. Epub 2009 Feb 20.
4
Characterization of the hyperrecombination phenotype of the pol3-t mutation of Saccharomyces cerevisiae.酿酒酵母pol3 - t突变体的超重组表型特征分析
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Genetic requirements for spontaneous and transcription-stimulated mitotic recombination in Saccharomyces cerevisiae.酿酒酵母中自发及转录刺激的有丝分裂重组的遗传要求。
Genetics. 2002 Sep;162(1):15-27. doi: 10.1093/genetics/162.1.15.
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The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells.结构特异性核酸内切酶Ercc1-Xpf是胚胎干细胞中靶向基因替换所必需的。
EMBO J. 2001 Nov 15;20(22):6540-9. doi: 10.1093/emboj/20.22.6540.
7
Induction of Ty recombination in yeast by cDNA and transcription: role of the RAD1 and RAD52 genes.cDNA和转录在酵母中诱导Ty重组:RAD1和RAD52基因的作用。
Genetics. 1996 Nov;144(3):947-55. doi: 10.1093/genetics/144.3.947.
8
Double-strand break-induced mitotic intrachromosomal recombination in the fission yeast Schizosaccharomyces pombe.双链断裂诱导的粟酒裂殖酵母有丝分裂染色体内重组
Genetics. 1996 Feb;142(2):341-57. doi: 10.1093/genetics/142.2.341.
9
Requirement of mismatch repair genes MSH2 and MSH3 in the RAD1-RAD10 pathway of mitotic recombination in Saccharomyces cerevisiae.酿酒酵母有丝分裂重组RAD1-RAD10途径中错配修复基因MSH2和MSH3的需求。
Genetics. 1996 Mar;142(3):727-36. doi: 10.1093/genetics/142.3.727.
10
Molecular genetic analysis of volatile-anesthetic action.挥发性麻醉药作用的分子遗传学分析
Mol Cell Biol. 1996 Jul;16(7):3446-53. doi: 10.1128/MCB.16.7.3446.

本文引用的文献

1
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
Recombinationless meiosis in Saccharomyces cerevisiae.酿酒酵母中的无重组减数分裂。
Mol Cell Biol. 1981 Oct;1(10):891-901. doi: 10.1128/mcb.1.10.891-901.1981.
4
Mitotic chromosome loss in a radiation-sensitive strain of the yeast Saccharomyces cerevisiae.酵母酿酒酵母辐射敏感菌株中的有丝分裂染色体丢失。
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5778-82. doi: 10.1073/pnas.78.9.5778.
5
Incision and postincision steps of pyrimidine dimer removal in excision-defective mutants of Saccharomyces cerevisiae.酿酒酵母切除缺陷型突变体中嘧啶二聚体去除的切割及切割后步骤。
J Bacteriol. 1981 Nov;148(2):618-23. doi: 10.1128/jb.148.2.618-623.1981.
6
Molecular mechanisms of pyrimidine dimer excision in Saccharomyces cerevisiae: incision of ultraviolet-irradiated deoxyribonucleic acid in vivo.酿酒酵母中嘧啶二聚体切除的分子机制:体内紫外线照射的脱氧核糖核酸的切割
J Bacteriol. 1981 May;146(2):692-704. doi: 10.1128/jb.146.2.692-704.1981.
7
The structure of the yeast ribosomal RNA genes. 2. The nucleotide sequence of the initiation site for ribosomal RNA transcription.酵母核糖体RNA基因的结构。2. 核糖体RNA转录起始位点的核苷酸序列。
Nucleic Acids Res. 1980 Nov 11;8(21):4919-26. doi: 10.1093/nar/8.21.4919.
8
The RAD52 gene is required for homothallic interconversion of mating types and spontaneous mitotic recombination in yeast.RAD52基因是酵母中交配型的同宗配合相互转换和自发有丝分裂重组所必需的。
Proc Natl Acad Sci U S A. 1980 Jan;77(1):503-7. doi: 10.1073/pnas.77.1.503.
9
Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiae.同宗配合型转换在酿酒酵母的rad52菌株中产生致死性染色体断裂。
Mol Cell Biol. 1981 Jun;1(6):522-34. doi: 10.1128/mcb.1.6.522-534.1981.
10
Changes in the chromosomal DNA of yeast during meiosis in repair mutants and the possible role of a deoxyribonuclease.修复突变体减数分裂过程中酵母染色体DNA的变化以及一种脱氧核糖核酸酶的可能作用。
Cold Spring Harb Symp Quant Biol. 1984;49:639-49. doi: 10.1101/sqb.1984.049.01.072.

酵母中RNA聚合酶I刺激的重组的遗传控制

Genetic control of RNA polymerase I-stimulated recombination in yeast.

作者信息

Zehfus B R, McWilliams A D, Lin Y H, Hoekstra M F, Keil R L

机构信息

Department of Biological Chemistry, Milton S. Hershey Medical Center, Hershey, Pennsylvania 17033.

出版信息

Genetics. 1990 Sep;126(1):41-52. doi: 10.1093/genetics/126.1.41.

DOI:10.1093/genetics/126.1.41
PMID:2227387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1204134/
Abstract

We examined the genetic control of the activity of HOT1, a cis-acting recombination-stimulatory sequence of Saccharomyces cerevisiae. Mutations in RAD1 and RAD52 decrease the ability of HOT1 to stimulate intrachromosomal recombination while mutations in RAD4 and RAD50 do not affect HOT1 activity. In rad1 delta strains, the stimulation of excisive recombination by HOT1 is decreased while the rate of gene replacement is not affected. In rad52-8 strains the ability of HOT1 to stimulate both excisive recombination and gene replacement is decreased. All of the recombinants in the rad52-8 strains that would be categorized as gene replacements based on their phenotype are diploids apparently derived by endomitosis and excisive recombination. Studies on rad1 delta rad52-8 strains show that these mutations interact synergistically in the presence or absence of HOT1, resulting in low levels of recombination. The rate of gene replacement but not excisive recombination is stimulated by HOT1 in rad1 delta rad52-8 strains. Taken together, the results show that HOT1 stimulates exchange using multiple recombination pathways. Some of the activity of HOT1 is RAD1-dependent, some is RAD52-dependent, and some requires either RAD1 or RAD52 as suggested by the synergistic interaction found in double mutant strains. There is also a component of HOT1 activity that is independent of both RAD1 and RAD52.

摘要

我们研究了酿酒酵母的顺式作用重组刺激序列HOT1活性的遗传控制。RAD1和RAD52中的突变会降低HOT1刺激染色体内重组的能力,而RAD4和RAD50中的突变不影响HOT1活性。在rad1δ菌株中,HOT1对切除性重组的刺激作用降低,而基因置换率不受影响。在rad52 - 8菌株中,HOT1刺激切除性重组和基因置换的能力均降低。rad52 - 8菌株中所有根据其表型被归类为基因置换的重组体都是明显通过核内有丝分裂和切除性重组产生的二倍体。对rad1δrad52 - 8菌株的研究表明,无论有无HOT1,这些突变都会协同作用,导致重组水平较低。在rad1δrad52 - 8菌株中,HOT1刺激基因置换率而非切除性重组率。综上所述,结果表明HOT1利用多种重组途径刺激交换。HOT1的一些活性依赖于RAD1,一些依赖于RAD52,还有一些如在双突变菌株中发现的协同相互作用所表明的那样,需要RAD1或RAD52。HOT1活性中也有一部分独立于RAD1和RAD52。