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衰老染色体端粒:使用末端重复序列和端粒相关DNA探针的平行研究。

Aging chromosome telomeres: parallel studies with terminal repeat and telomere associated DNA probes.

作者信息

Benn P

机构信息

Department of Pediatrics, University of Connecticut Health Center, Farmington 06030-6140, USA.

出版信息

Mech Ageing Dev. 1997 Dec 15;99(2):153-66. doi: 10.1016/s0047-6374(97)00099-7.

DOI:10.1016/s0047-6374(97)00099-7
PMID:9483489
Abstract

Human chromosome telomeres consist of tandemly repeated (TTAGGG)n sequences with variant and more complex telomere-associated DNA sequences proximal to the terminal repeats. Terminal restriction fragment (TRF) sizes have been evaluated by Southern blot analysis using a terminal repeat probe, (TTAGGG)3 that will simultaneously detect all telomeres and with a telomere-associated DNA probe, TelBamll, that identifies a specific sub-group of chromosome ends. For DNA extracted from in vitro aging fibroblasts, a progressive reduction in the size of the TRFs could be demonstrated using both probes. For both fibroblasts and adult lymphocyte DNA, there were differences in the size of the fragments detected with the two probes. Studies were carried out to determine whether this difference might, in part, be attributable to variability in terminal repeat lengths as well as heterogeneity in the location of terminal restriction enzyme recognition sites. Using the (TTAGGG)3 probe to identify all telomeres, the terminal repeat lengths from lymphocytes of two adults appeared to be highly variable with sizes upto 20 kb. For the sub-group of telomeres identified by TelBamll the terminal repeat lengths were estimated to be 2-4 kb and appeared to show relatively little size diversity. If it assumed that the molecular weights of the DNA fragments identified in these studies do accurately reflect individual telomere structures, then it can be concluded that some specific telomere repeat arrays are substantially shorter than others. Variation in terminal repeat length may be related to the extent that telomeres participate in chromosome rearrangement.

摘要

人类染色体端粒由串联重复的(TTAGGG)n序列组成,在末端重复序列近端存在变异且更为复杂的端粒相关DNA序列。通过使用末端重复探针(TTAGGG)3进行Southern印迹分析来评估末端限制片段(TRF)的大小,该探针可同时检测所有端粒,还使用了端粒相关DNA探针TelBamll,它可识别特定的染色体末端亚组。对于从体外老化成纤维细胞中提取的DNA,使用这两种探针均可证明TRF大小的逐渐减小。对于成纤维细胞和成人淋巴细胞DNA,用这两种探针检测到的片段大小存在差异。开展研究以确定这种差异是否部分归因于末端重复长度的变异性以及末端限制酶识别位点位置的异质性。使用(TTAGGG)3探针识别所有端粒,两名成年人淋巴细胞的末端重复长度似乎高度可变,大小可达20 kb。对于由TelBamll识别的端粒亚组,末端重复长度估计为2 - 4 kb,且大小多样性相对较小。如果假设这些研究中鉴定出的DNA片段的分子量确实准确反映了个体端粒结构,那么可以得出结论,一些特定的端粒重复阵列比其他阵列短得多。末端重复长度的变化可能与端粒参与染色体重排的程度有关。

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