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在酿酒酵母交配型转换过程中,SBF(Swi4/Swi6)和Fkh1对供体偏好的细胞周期依赖性调控

Cell cycle-dependent regulation of Saccharomyces cerevisiae donor preference during mating-type switching by SBF (Swi4/Swi6) and Fkh1.

作者信息

Coïc Eric, Sun Kaiming, Wu Cherry, Haber James E

机构信息

Department of Biology and Rosenstiel Center, Brandeis University, Waltham, MA 02254-9110, USA.

出版信息

Mol Cell Biol. 2006 Jul;26(14):5470-80. doi: 10.1128/MCB.02443-05.

Abstract

Saccharomyces mating-type switching occurs through a double-strand break-initiated gene conversion event at MAT, using one of two donors located distantly on the same chromosome, HMLalpha and HMRa. MATa cells preferentially choose HMLalpha, a decision that depends on the recombination enhancer (RE) that controls recombination along the left arm of chromosome III. We previously showed that an fhk1Delta mutation reduces HMLalpha usage in MATa cells, but not to the level seen when RE is deleted. We now report that donor preference also depends on binding of the Swi4/Swi6 (SBF) transcription factors to an evolutionarily conserved SCB site within RE. As at other SCB-containing promoters, SBF binds to RE in the G(1) phase. Surprisingly, Fkh1 binds to RE only in G(2), which contrasts with its cell cycle-independent binding to its other target promoters. SBF and Fkh1 define two independent RE activation pathways, as deletion of both Fkh1 and SCB results in nearly complete loss of HML usage in MATa cells. These transcription factors create an epigenetic modification of RE in a fashion that apparently does not involve transcription. In addition, the putative helicase Chl1, previously involved in donor preference, functions in the SBF pathway.

摘要

酿酒酵母的交配型转换通过MAT位点处双链断裂引发的基因转换事件发生,使用位于同一条染色体上远处的两个供体之一,即HMLα和HMRa。MATa细胞优先选择HMLα,这一决定取决于控制III号染色体左臂重组的重组增强子(RE)。我们之前表明,fhk1Δ突变会降低MATa细胞中HMLα的使用频率,但不会降至RE缺失时的水平。我们现在报告,供体偏好还取决于Swi4/Swi6(SBF)转录因子与RE内进化保守的SCB位点的结合。与其他含SCB的启动子一样,SBF在G1期与RE结合。令人惊讶的是,Fkh1仅在G2期与RE结合,这与其对其他靶启动子的细胞周期非依赖性结合形成对比。SBF和Fkh1定义了两条独立的RE激活途径,因为Fkh1和SCB的缺失会导致MATa细胞中HML使用几乎完全丧失。这些转录因子以一种显然不涉及转录的方式对RE进行表观遗传修饰。此外,先前参与供体偏好的推定解旋酶Chl1在SBF途径中起作用。

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