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植物端粒上G链悬垂结构的分析:两种不同端粒结构的证据

Analysis of the G-overhang structures on plant telomeres: evidence for two distinct telomere architectures.

作者信息

Riha K, McKnight T D, Fajkus J, Vyskot B, Shippen D E

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128, USA.

出版信息

Plant J. 2000 Sep;23(5):633-41. doi: 10.1046/j.1365-313x.2000.00831.x.

DOI:10.1046/j.1365-313x.2000.00831.x
PMID:10972889
Abstract

Telomeres are highly conserved structures essential for maintaining the integrity of eukaryotic genomes. In yeast, ciliates and mammals, the G-rich strand of the telomere forms a 3' overhang on the chromosome terminus. Here we investigate the architecture of telomeres in the dicot plants Silene latifolia and Arabidopsis thaliana using the PENT (primer extension/nick translation) assay. We show that both Arabidopsis and Silene telomeres carry G-overhangs longer than 20-30 nucleotides. However, in contrast to yeast and ciliate telomeres, only half of the telomeres in Silene seedlings possess detectable G-overhangs. PENT reactions using a variety of primers and reaction conditions revealed that the remaining fraction of Silene telomeres carries either no overhangs or overhangs less than 12 nucleotides in length. G-overhangs were observed in Silene seeds and leaves, tissues that lack telomerase activity. These findings suggest that incomplete DNA replication of the lagging strand, rather than synthesis by telomerase, is the primary mechanism for G-overhang synthesis in plants. Unexpectedly, we found that the fraction of telomeres with detectable G-overhangs decreased from 50% in seedlings to 35% in leaves. The difference may reflect increased susceptibility of the G-overhangs to nuclease attack in adult leaves, an event that could act as a precursor for the catabolic processes accompanying leaf senescence

摘要

端粒是高度保守的结构,对于维持真核生物基因组的完整性至关重要。在酵母、纤毛虫和哺乳动物中,端粒富含G的链在染色体末端形成3'端突出。在这里,我们使用PENT(引物延伸/缺口平移)分析法研究双子叶植物宽叶蝇子草和拟南芥中端粒的结构。我们发现,拟南芥和蝇子草的端粒都带有长度超过20 - 30个核苷酸的G端突出。然而,与酵母和纤毛虫的端粒不同,蝇子草幼苗中只有一半的端粒具有可检测到的G端突出。使用多种引物和反应条件进行的PENT反应表明,蝇子草端粒的其余部分要么没有端突出,要么端突出长度小于12个核苷酸。在缺乏端粒酶活性的蝇子草种子和叶片组织中观察到了G端突出。这些发现表明,滞后链的不完全DNA复制而非端粒酶的合成是植物中G端突出合成的主要机制。出乎意料的是,我们发现具有可检测到的G端突出的端粒比例从幼苗中的50%降至叶片中的35%。这种差异可能反映了成年叶片中G端突出对核酸酶攻击的敏感性增加,这一事件可能是伴随叶片衰老的分解代谢过程的前兆。

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