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首页> 外文期刊>Molecular and Cellular Biology >Rad51-Dependent Aberrant Chromosome Structures at Telomeres and Ribosomal DNA Activate the Spindle Assembly Checkpoint
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Rad51-Dependent Aberrant Chromosome Structures at Telomeres and Ribosomal DNA Activate the Spindle Assembly Checkpoint

机译:Rad51依赖于端粒和核糖体DNA的异常染色体结构激活了主轴装配检查点。

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The spindle assembly checkpoint (SAC) monitors defects in kinetochore-microtubule attachment or lack of tension at kinetochores and arrests cells at prometaphase. In fission yeast, the double mutant between pot1Δ and the helicase-dead point mutant of the RecQ helicase Rqh1 gene (rqh1-hd) accumulates Rad51-dependent recombination intermediates at telomeres and enters mitosis with those intermediates. Here, we found that SAC-dependent prometaphase arrest occurred more frequently in pot1Δ rqh1-hd double mutants than in rqh1-hd single mutants. SAC-dependent prometaphase arrest also occurred more frequently in rqh1-hd single mutants after cells were released from DNA replication block compared to the rqh1-hd single mutant in the absence of exogenous insult to the DNA. In both cases, Mad2 foci persisted longer than usual at kinetochores, suggesting a defect in kinetochore-microtubule attachment. In pot1Δ rqh1-hd double mutants and rqh1-hd single mutants released from DNA replication block, SAC-dependent prometaphase arrest was suppressed by the removal of the recombination or replication intermediates. Our results indicate that the accumulation of recombination or replication intermediates induces SAC-dependent prometaphase arrest, possibly by affecting kinetochore-microtubule attachment.
机译:纺锤体装配检查点(SAC)可以监测动线粒体-微管附件中的缺陷或动植物的张力不足,并将细胞停在前中期。在裂变酵母中, pot1 Δ和RecQ解旋酶Rqh1基因的解旋酶死点突变体( rqh1-hd )之间的双突变体在端粒处积累了Rad51依赖的重组中间体。并与这些中间体一起进入有丝分裂。在这里,我们发现与 rqh1-hd 单突变体相比,与 rqh1-hd 单突变体相比,依赖SAC的前中期停滞发生的频率更高。在没有外源存在的情况下,与 rqh1-hd 单个突变体相比,从DNA复制区释放细胞后, rqh1-hd 单个突变体中SAC依赖的前中期停滞也更加频繁。对DNA的侮辱。在这两种情况下,Mad2病灶在动植物中持续的时间都比平常长,这表明动线粒体-微管附件存在缺陷。在从DNA复制区释放的pot1Δrqh1-hd 双突变体和 rqh1-hd 单突变体中,通过去除重组或复制中间体抑制了SAC依赖的前中期阻滞。我们的结果表明,重组或复制中间体的积累可能诱导SAC依赖的前中期停滞,可能是通过影响动线粒体-微管的附着而引起的。

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