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Telomere-Telomere Recombination Is an Efficient Bypass Pathway for Telomere Maintenance in Saccharomyces cerevisiae

机译:端粒-端粒重组是酿酒酵母端粒维持的有效旁路途径。

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摘要

Many Saccharomyces telomeres bear one or more copies of the repetitive Y′ element followed by ∼350 bp of telomerase-generated C1–3A/TG1–3 repeats. Although most cells lacking a gene required for the telomerase pathway die after 50 to 100 cell divisions, survivors arise spontaneously in such cultures. These survivors have one of two distinct patterns of telomeric DNA (V. Lundblad and E. H. Blackburn, Cell 73:347–360, 1993). The more common of the two patterns, seen in type I survivors, is tandem amplification of Y′ followed by very short tracts of C1–3A/TG1–3 DNA. By determining the structure of singly tagged telomeres, chromosomes in type II survivors were shown to end in very long and heterogeneous-length tracts of C1–3A/TG1–3 DNA, with some telomeres having 12 kb or more of C1–3A/TG1–3 repeats. Maintenance of these long telomeres required the continuous presence of Rad52p. Whereas type I survivors often converted to the type II structure of telomeric DNA, the type II pattern was maintained for at least 250 cell divisions. However, during outgrowth, the structure of type II telomeres was dynamic, displaying gradual shortening as well as other structural changes that could be explained by continuous gene conversion events with other telomeres. Although most type II survivors had a growth rate similar to that of telomerase-proficient cells, their telomeres slowly returned to wild-type lengths when telomerase was reintroduced. The very long and heterogeneous-length telomeres characteristic of type II survivors in Saccharomyces are reminiscent of the telomeres in immortal human cell lines and tumors that maintain telomeric DNA in the absence of telomerase.
机译:许多酿酒酵母的端粒带有一个或多个重复的Y'元件,然后是约350 bp的端粒酶生成的C1-3A / TG1-3重复序列。尽管大多数缺少端粒酶途径所需基因的细胞会在50到100个细胞分裂后死亡,但存活者会在这种培养物中自发出现。这些幸存者具有两种不同的端粒DNA模式之一(V. Lundblad和E. H. Blackburn,Cell 73:347-360,1993)。在I型幸存者中看到的两种模式中最常见的是Y'串联扩增,然后是非常短的C1-3A / TG1-3 DNA。通过确定单个标记端粒的结构,II型幸存者的染色体显示在非常长且异质的C1-3A / TG1-3 DNA末端,某些端粒具有12 kb或更多的C1-3A / TG1 –3重复。这些长端粒的维持需要Rad52p的持续存在。 I型幸存者通常会转换为端粒DNA的II型结构,而II型模式则至少维持了250个细胞分裂。然而,在生长过程中,II型端粒的结构是动态的,显示出逐渐缩短以及其他结构变化,这可以用与其他端粒的连续基因转化事件来解释。尽管大多数II型幸存者的生长速率与端粒酶熟练的细胞相似,但是当重新引入端粒酶时,它们的端粒缓慢恢复到野生型长度。酵母菌中II型幸存者的特征是非常长且异质长度的端粒,让人想起永生的人类细胞系和不存在端粒酶而维持端粒DNA的肿瘤中的端粒。

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