...
首页> 外文期刊>eLife journal >Multiple kinases inhibit origin licensing and helicase activation to ensure reductive cell division during meiosis
【24h】

Multiple kinases inhibit origin licensing and helicase activation to ensure reductive cell division during meiosis

机译:多种激酶抑制起源许可和解旋酶激活,以确保减数分裂过程中的还原性细胞分裂

获取原文
           

摘要

Meiotic cells undergo a single round of DNA replication followed by two rounds of chromosome segregation (the meiotic divisions) to produce haploid gametes. Both DNA replication and chromosome segregation are similarly regulated by CDK oscillations in mitotic cells. Yet how these two events are uncoupled between the meiotic divisions is unclear. Using Saccharomyces cerevisiae , we show that meiotic cells inhibit both helicase loading and helicase activation to prevent DNA replication between the meiotic divisions. CDK and the meiosis–specific kinase Ime2 cooperatively inhibit helicase loading, and their simultaneous inhibition allows inappropriate helicase reloading. Further analysis uncovered two previously unknown mechanisms by which Ime2 inhibits helicase loading. Finally, we show that CDK and the polo–like kinase Cdc5 trigger degradation of Sld2, an essential helicase–activation protein. Together, our data demonstrate that multiple kinases inhibit both helicase loading and activation between the meiotic divisions, thereby ensuring reductive cell division.
机译:减数分裂细胞经历单轮DNA复制,然后经历两轮染色体分离(减数分裂),产生单倍体配子。 DNA复制和染色体分离均受有丝分裂细胞中CDK振荡的类似调节。尚不清楚减数分裂之间如何将这两个事件联系在一起。使用酿酒酵母,我们显示减数分裂细胞抑制解旋酶负载和解旋酶激活,以防止减数分裂分裂之间的DNA复制。 CDK和减数分裂特异性激酶Ime2协同抑制解旋酶负载,同时抑制它们可导致不适当的解旋酶负载。进一步的分析发现了Ime2抑制解旋酶负载的两种先前未知的机制。最后,我们表明CDK和polo样激酶Cdc5触发了Sld2的降解,Sld2是必不可少的解旋酶激活蛋白。总之,我们的数据表明多种激酶既抑制解旋酶的负载,又抑制减数分裂之间的活化,从而确保还原性细胞分裂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号