Thon G, Klar A J
NCI-Frederick Cancer Research and Development Center, ABL-Basic Research Program, Maryland 21702-1201.
Genetics. 1993 Aug;134(4):1045-54. doi: 10.1093/genetics/134.4.1045.
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.
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。