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一个DNA复制停滞位点RTS1通过确定粟酒裂殖酵母中mat1处的复制方向来调控印记。

A DNA replication-arrest site RTS1 regulates imprinting by determining the direction of replication at mat1 in S. pombe.

作者信息

Dalgaard J Z, Klar A J

机构信息

Marie Curie Research Institute (MCRI), The Chart, Oxted, Surrey RH8 0TL, UK.

出版信息

Genes Dev. 2001 Aug 15;15(16):2060-8. doi: 10.1101/gad.200801.

Abstract

Mating-type switching in Schizosaccharomyces pombe involves a strand-specific, alkali-labile imprint at the mat1 (mating-type) locus. The imprint is synthesized during replication in a swi1, swi3, and polymerase alpha (swi7) dependent manner and is dependent on mat1 being replicated in a specific direction. Here we show that the direction of replication at mat1 is controlled by a cis-acting polar terminator of replication (RTS1). Two-dimensional gel analysis of replication intermediates reveals that RTS1 only terminates replication forks moving in the centromere-distal direction. A genetic analysis shows that RTS1 optimizes the imprinting process. Transposing the RTS1 element to the distal side of mat1 abolishes imprinting of the native mat1 allele but restores imprinting of an otherwise unimprinted inverted mat1 allele. These data provide conclusive evidence for the "direction of replication model" that explains the asymmetrical switching pattern of S. pombe, and identify a DNA replication-arrest element implicated in a developmental process. Such elements could play a more general role during development and differentiation in higher eukaryotes by regulating the direction of DNA replication at key loci.

摘要

粟酒裂殖酵母中的交配型转换涉及mat1(交配型)位点的链特异性、碱不稳定印记。该印记在复制过程中以依赖swi1、swi3和聚合酶α(swi7)的方式合成,并且依赖于mat1以特定方向进行复制。在这里,我们表明mat1处的复制方向由顺式作用的极性复制终止子(RTS1)控制。对复制中间体的二维凝胶分析表明,RTS1仅终止向着丝粒远端方向移动的复制叉。遗传分析表明,RTS1优化了印记过程。将RTS1元件转座到mat1的远端会消除天然mat1等位基因的印记,但会恢复原本未印记的反向mat1等位基因的印记。这些数据为解释粟酒裂殖酵母不对称转换模式的“复制方向模型”提供了确凿证据,并鉴定出一个与发育过程相关的DNA复制停滞元件。通过调节关键位点的DNA复制方向,此类元件可能在高等真核生物的发育和分化过程中发挥更普遍的作用。

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