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猪蛔虫染色质消减过程中的新端粒形成。

New telomere formation during the process of chromatin diminution in Ascaris suum.

作者信息

Jentsch Stephan, Tobler Heinz, Müller Fritz

机构信息

Institute of Zoology, University of Fribourg, Switzerland.

出版信息

Int J Dev Biol. 2002 Jan;46(1):143-8.

PMID:11902675
Abstract

Chromatin diminution in the parasitic nematode Ascaris suum represents an interesting case of developmentally programmed DNA rearrangement in higher eukaryotes. At the molecular level, it is a rather complex event including chromosome breakage, new telomere formation and DNA degradation. Analysis of a cloned somatic telomere (pTel1) revealed that it has been newly created during the process of chromatin diminution by the addition of telomeric repeats (TTAGGC)n to a chromosomal breakage site (Müller et al., 1991). However, telomere addition does not occur at a single chromosomal locus, but at many different sites within a short chromosomal region, termed CBR1 (chromosomal breakage region 1). Here we present the cloning and the analysis of 83 different PCR amplified telomere addition sites from the region of CBR1. The lack of any obvious sequence homology shared among them argues for a telomerase-mediated healing process, rather than for a recombinational event. This hypothesis is strongly supported by the existence of 1-6 nucleotides corresponding to and being in frame with the newly added telomeric repeats at almost all of the telomere addition sites. Furthermore, we show that telomeres are not only added to the ends of the retained chromosomal portions, but also to the eliminated part of the chromosomes, which later on become degraded in the cytoplasm. This result suggests that de novo telomere formation during the process of chromatin diminution represents a non-specific process which can heal any broken DNA end.

摘要

寄生线虫猪蛔虫体内的染色质消减是高等真核生物中发育程序控制的DNA重排的一个有趣例子。在分子水平上,这是一个相当复杂的事件,包括染色体断裂、新端粒形成和DNA降解。对一个克隆的体细胞端粒(pTel1)的分析表明,它是在染色质消减过程中通过在染色体断裂位点添加端粒重复序列(TTAGGC)n而新形成的(Müller等人,1991年)。然而,端粒添加并非发生在单个染色体位点,而是发生在一个短染色体区域内的许多不同位点,该区域称为CBR1(染色体断裂区域1)。在此,我们展示了从CBR1区域克隆并分析了83个不同的PCR扩增端粒添加位点。它们之间缺乏任何明显的序列同源性,这表明是端粒酶介导的修复过程,而非重组事件。几乎所有端粒添加位点都存在与新添加的端粒重复序列相对应且读码框一致的1 - 6个核苷酸,这一发现有力地支持了这一假说。此外,我们还表明,端粒不仅添加到保留的染色体部分的末端,也添加到染色体被消除的部分,这些部分随后在细胞质中被降解。这一结果表明,染色质消减过程中的端粒从头形成是一个非特异性过程,能够修复任何断裂的DNA末端。

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