首页> 外文期刊>Journal of Cell Science >A product of the bicistronic Drosophila melanogaster gene CG31241, which also encodes a trimethylguanosine synthase, plays a role in telomere protection.
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A product of the bicistronic Drosophila melanogaster gene CG31241, which also encodes a trimethylguanosine synthase, plays a role in telomere protection.

机译:双透号果蝇黑色素转移基因CG31241的产物也编码三甲基胍合酶,起代粒体保护作用。

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摘要

Although telomere formation occurs through a different mechanism in Drosophila compared with other organisms, telomere associations result from mutations in homologous genes, indicating the involvement of similar pathways in chromosome end protection. We report here that mutations of the Drosophila melanogaster gene CG31241 lead to high frequency chromosome end fusions. CG31241 is a bicistronic gene that encodes trimethylguanosine synthase (TGS1), which forms the m3G caps of noncoding small RNAs, and a novel protein, DTL. We show that although TGS1 has no role in telomere protection, DTL is localized at specific sites, including the ends of polytene chromosomes, and its loss results in telomere associations. Mutations of ATM- and Rad3-related (ATR) kinase suppress telomere fusions in the absence of DTL. Thus, genetic interactions place DTL in an ATR-related pathway in telomere protection. In contrast to ATR kinase, mutations of ATM (ataxia telangiectasia mutated) kinase, which acts in a partially overlapping pathway of telomere protection, do not suppress formation of telomere associations in the absence of DTL. Thus, uncovering the role of DTL will help to dissect the evolutionary conserved pathway(s) controlling ATM-ATR-related telomere protection.
机译:尽管与其他生物相比,通过果蝇的不同机制发生了端粒形成,但端粒缔组织是由同源基因的突变产生的,表明相似途径在染色体最终保护中的累积。我们在此报道,果蝇黑素转基团基因CG31241的突变导致高频染色体最终融合。 CG31241是编码三甲基胍氨酸合酶(TGS1)的双顺声基因,其形成非编码小RNA的M3G帽,以及新的蛋白质DTL。我们表明,尽管TGS1在端粒保护中没有作用,但DTL在特定部位定位,包括聚直系染色体的末端,其损失导致端粒关联产生。在没有DTL的情况下,ATM-和RAD3相关(ATR)激酶的突变抑制了端粒融合。因此,遗传相互作用在端粒保护中的ATR相关途径中的DTL。与ATR激酶相比,ATM(Ataxia Telanciectasia突变)激酶的突变作用于端粒保护的部分重叠途径,不会在不存在DTL的情况下抑制端粒缔代性的形成。因此,揭示DTL的作用将有助于对控制ATM-ATR相关的端粒保护的进化保守途径进行解剖。

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