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The Structure-Specific Endonucleases MUS81 and SEND1 Are Essential for Telomere Stability in Arabidopsis

机译:特定结构的核酸内切酶MUS81和SEND1对于拟南芥端粒稳定性至关重要。

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Structure-specific endonucleases act to repair potentially toxic structures produced by recombination and DNA replication, ensuring proper segregation of the genetic material to daughter cells during mitosis and meiosis. Arabidopsis thaliana has two putative homologs of the resolvase (structure-specific endonuclease): GEN1/Yen1. Knockout of resolvase genes GEN1 and SEND1, individually or together, has no detectable effect on growth, fertility, or sensitivity to DNA damage. However, combined absence of the endonucleases MUS81 and SEND1 results in severe developmental defects, spontaneous cell death, and genome instability. A similar effect is not seen in mus81 gen1 plants, which develop normally and are fertile. Absence of RAD51 does not rescue mus81 send1, pointing to roles of these proteins in DNA replication rather than DNA break repair. The enrichment of S-phase histone g-H2AX foci and a striking loss of telomeric DNA in mus81 send1 further support this interpretation. SEND1 has at most a minor role in resolution of the Holliday junction but acts as an essential backup to MUS81 for resolution of toxic replication structures to ensure genome stability and to maintain telomere integrity.
机译:结构特异性核酸内切酶可修复重组和DNA复制产生的潜在毒性结构,从而确保在有丝分裂和减数分裂过程中遗传物质与子代细胞的正确分离。拟南芥(Arabidopsis thaliana)有两个假定的解析酶同源物(结构特异性核酸内切酶):GEN1 / Yen1。单独或一起敲除分辨酶基因GEN1和SEND1,对生长,繁殖力或对DNA损伤的敏感性均无可检测的影响。但是,核酸内切酶MUS81和SEND1的联合缺失会导致严重的发育缺陷,自发细胞死亡和基因组不稳定。在mus81 gen1植物中未观察到类似的效果,该植物正常发育且可育。缺少RAD51不能拯救mus81 send1,这表明这些蛋白质在DNA复制而不是DNA断裂修复中的作用。 mus81 send1中S期组蛋白g-H2AX灶的富集和端粒DNA的惊人丢失进一步支持了这一解释。 SEND1在霍利迪结的解析中至多起很小的作用,但作为MUS81的基本备份,用于解析毒性复制结构,以确保基因组稳定性和维持端粒完整性。

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