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Maintenance of Very Long Telomeres by Recombination in the Kluyveromyces lactis stn1-M1 Mutant Involves Extreme Telomeric Turnover Telomeric Circles and Concerted Telomeric Amplification

机译:通过重组在乳酸克鲁维酵母stn1-M1突变体中维持非常长的端粒涉及极端端粒转换端粒环和协同端粒扩增。

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摘要

Some cancers utilize the recombination-dependent process of alternative lengthening of telomeres (ALT) to maintain long heterogeneous telomeres. Here, we studied the recombinational telomere elongation (RTE) of the Kluyveromyces lactis stn1-M1 mutant. We found that the total amount of the abundant telomeric DNA in stn1-M1 cells is subject to rapid variation and that it is likely to be primarily extrachromosomal. Rad50 and Rad51, known to be required for different RTE pathways in Saccharomyces cerevisiae, were not essential for the production of either long telomeres or telomeric circles in stn1-M1 cells. Circles of DNA containing telomeric repeats (t-circles) either present at the point of establishment of long telomeres or introduced later into stn1-M1 cells each led to the formation of long tandem arrays of the t-circle's sequence, which were incorporated at multiple telomeres. These tandem arrays were extraordinarily unstable and showed evidence of repeated rounds of concerted amplification. Our results suggest that the maintenance of telomeres in the stn1-M1 mutant involves extreme turnover of telomeric sequences from processes including both large deletions and the copying of t-circles.
机译:一些癌症利用端粒替代性延长的重组依赖过程来维持较长的异质端粒。在这里,我们研究了乳酸克鲁维酵母stn1-M1突变体的重组端粒延长(RTE)。我们发现,stn1-M1细胞中大量端粒DNA的总量会快速变化,并且很可能主要是染色体外的。 Rad50和Rad51,已知是酿酒酵母中不同RTE途径所必需的,对于在stn1-M1细胞中产生长端粒或端粒环不是必需的。包含端粒重复序列的DNA环(t环)或者出现在长端粒的建立点,或者后来引入stn1-M1细胞中,每个都导致t环序列的长串联阵列的形成,并以多个序列掺入端粒。这些串联阵列非常不稳定,并显示出重复的一轮协同扩增的证据。我们的结果表明,stn1-M1突变体中端粒的维持涉及端粒端粒的极端更新,该端粒端粒来自包括大缺失和t环复制在内的过程。

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