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Dyskerin Is a Component of the Arabidopsis Telomerase RNP Required for Telomere Maintenance

机译:Dyskerin是维持端粒所需的拟南芥端粒酶RNP的组成部分

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Dyskerin binds the H/ACA box of human telomerase RNA and is a core telomerase subunit required for RNP biogenesis and enzyme function in vivo. Missense mutations in dyskerin result in dyskeratosis congenita, a complex syndrome characterized by bone marrow failure, telomerase enzyme deficiency, and progressive telomere shortening. Here we demonstrate that dyskerin also contributes to telomere maintenance in Arabidopsis thaliana. We report that both AtNAP57, the Arabidopsis dyskerin homolog, and AtTERT, the telomerase catalytic subunit, accumulate in the plant nucleolus, and AtNAP57 associates with active telomerase RNP particles in an RNA-dependent manner. Furthermore, AtNAP57 interacts in vitro with AtPOT1a, a novel component of Arabidopsis telomerase. Although a null mutation in AtNAP57 is lethal, AtNAP57, like AtTERT, is not haploinsufficient for telomere maintenance in Arabidopsis. However, introduction of an AtNAP57 allele containing a T66A mutation decreased telomerase activity in vitro, disrupted telomere length regulation on individual chromosome ends in vivo, and established a new, shorter telomere length set point. These results imply that T66A NAP57 behaves as a dominant-negative inhibitor of telomerase. We conclude that dyskerin is a conserved component of the telomerase RNP complex in higher eukaryotes that is required for maximal enzyme activity in vivo.
机译:Dyskerin与人端粒酶RNA的H / ACA盒结合,是体内RNP生物发生和酶功能所需的核心端粒酶亚基。 dyskerin的错义突变会导致先天性keratka病,这是一种复杂的综合征,其特征是骨髓衰竭,端粒酶缺乏和端粒缩短。在这里,我们证明了dyskerin也有助于拟南芥中端粒的维持。我们报告说,AtNAP57,拟南芥 dyskerin同源物,和AtTERT,端粒酶催化亚基,在植物核仁中积累,并且AtNAP57与活性端粒酶RNP颗粒以RNA依赖的方式缔合。此外,AtNAP57在体外与拟南芥端粒酶的新型成分AtPOT1a相互作用。尽管 AtNAP57 中的无效突变是致命的,但与AtTERT一样,AtNAP57也不能单倍地维持拟南芥中的端粒。但是,引入含有T66A突变的 AtNAP57 等位基因会降低体外的端粒酶活性,破坏体内单个染色体末端的端粒长度调节,并建立一个新的,较短的端粒长度设定点。这些结果暗示T66A NAP57充当端粒酶的显性负抑制剂。我们得出结论,dyskerin是高等真核生物中端粒酶RNP复合物的保守成分,是体内最大酶活性所必需的。

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