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Directionality of fission yeast mating-type interconversion is controlled by the location of the donor loci.裂殖酵母交配型相互转换的方向性由供体位点的位置控制。
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2
A recombinationally repressed region between mat2 and mat3 loci shares homology to centromeric repeats and regulates directionality of mating-type switching in fission yeast.mat2和mat3基因座之间的重组抑制区域与着丝粒重复序列具有同源性,并调节裂殖酵母中交配型转换的方向性。
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The switching gene swi6 affects recombination and gene expression in the mating-type region of Schizosaccharomyces pombe.开关基因swi6影响粟酒裂殖酵母交配型区域的重组和基因表达。
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Heterochromatin regulates cell type-specific long-range chromatin interactions essential for directed recombination.异染色质调控细胞类型特异性的远距离染色质相互作用,这对于定向重组至关重要。
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Fission yeast Swi2 designates cell-type specific donor and stimulates Rad51-driven strand exchange for mating-type switching.裂殖酵母 Swi2 可指定细胞类型特异性供体,并刺激 Rad51 驱动的链交换,以实现交配型转换。
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本文引用的文献

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Studies on recombination in Schizosaccharomyces pombe.粟酒裂殖酵母中的重组研究。
Cold Spring Harb Symp Quant Biol. 1958;23:161-70. doi: 10.1101/sqb.1958.023.01.020.
2
DNA polymerase-alpha is essential for mating-type switching in fission yeast.DNA聚合酶α对于裂殖酵母中的交配型转换至关重要。
Nature. 1993 Jan 21;361(6409):271-3. doi: 10.1038/361271a0.
3
Genes required for initiation and resolution steps of mating-type switching in fission yeast.裂殖酵母中交配型转换起始和终止步骤所需的基因。
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Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
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Rearrangements of the transposable mating-type cassettes of fission yeast.裂殖酵母可转座交配型盒式结构的重排。
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Genes involved in meiosis and sporulation of a yeast.参与酵母减数分裂和孢子形成的基因。
Mol Gen Genet. 1968;102(4):301-6. doi: 10.1007/BF00433721.
7
Replicating plasmids in Schizosaccharomyces pombe: improvement of symmetric segregation by a new genetic element.在粟酒裂殖酵母中复制质粒:一种新的遗传元件对对称分离的改善
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Four mating-type genes control sexual differentiation in the fission yeast.四个交配型基因控制裂殖酵母中的性别分化。
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9
Mapping the double-strand breaks at the mating-type locus in fission yeast by genomic sequencing.通过基因组测序绘制裂殖酵母交配型位点的双链断裂图谱。
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10
The developmental fate of fission yeast cells is determined by the pattern of inheritance of parental and grandparental DNA strands.裂殖酵母细胞的发育命运由亲代和祖代DNA链的遗传模式决定。
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裂殖酵母交配型相互转换的方向性由供体位点的位置控制。

Directionality of fission yeast mating-type interconversion is controlled by the location of the donor loci.

作者信息

Thon G, Klar A J

机构信息

NCI-Frederick Cancer Research and Development Center, ABL-Basic Research Program, Maryland 21702-1201.

出版信息

Genetics. 1993 Aug;134(4):1045-54. doi: 10.1093/genetics/134.4.1045.

DOI:10.1093/genetics/134.4.1045
PMID:8375648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1205573/
Abstract

Cells of homothallic strains of Schizosaccharomyces pombe efficiently switch between two mating types called P and M. The phenotypic switches are due to conversion of the expressed mating-type locus (mat1) by two closely linked silent loci, mat2-P and mat3-M, that contain unexpressed information for the P and M mating types, respectively. In this process, switching-competent cells switch to the opposite mating type in 72-90% of the cell divisions. Hence, mat2-P is a preferred donor of information to mat1 in M cells, whereas mat3-M is a preferred donor in P cells. We investigated the reason for the donor preference by constructing a strain in which the genetic contents of the donor loci were swapped. We found that switching to the opposite mating type was very inefficient in that strain. This shows that the location of the silent cassettes in the chromosome, rather than their content, is the deciding factor for recognition of the donor for each cell type. We propose a model in which switching is achieved by regulating accessibility of the donor loci, perhaps by changing the chromatin structure in the mating-type region, thus promoting an intrachromosomal folding of mat2 or mat3 onto mat1 in a cell type-specific fashion. We also present evidence for the involvement of the Swi6 and Swi6-mod trans-acting factors in the donor-choice mechanism. We suggest that these factors participate in forming the proposed folded structure.

摘要

粟酒裂殖酵母同宗配合菌株的细胞能在称为P型和M型的两种交配型之间高效转换。表型转换是由于表达的交配型基因座(mat1)被两个紧密连锁的沉默基因座mat2-P和mat3-M转换,这两个基因座分别包含P型和M型交配型的未表达信息。在这个过程中,具有转换能力的细胞在72%至90%的细胞分裂中转换为相反的交配型。因此,mat2-P是M细胞中mat1的首选信息供体,而mat3-M是P细胞中的首选供体。我们通过构建一个供体基因座遗传内容被交换的菌株来研究供体偏好的原因。我们发现,在该菌株中转换为相反的交配型效率非常低。这表明沉默盒在染色体上的位置,而非其内容,是每种细胞类型识别供体的决定因素。我们提出了一个模型,其中转换是通过调节供体基因座的可及性来实现的,可能是通过改变交配型区域的染色质结构,从而以细胞类型特异性的方式促进mat2或mat3在染色体内部折叠到mat1上。我们还提供了Swi6和Swi6-mod反式作用因子参与供体选择机制的证据。我们认为这些因子参与形成了所提出的折叠结构。