Laboratory for Molecular and Cell Biology, Department of Molecular Biology, Ruđer Bošković Institute, Zagreb, Croatia.
Biogerontology. 2012 Apr;13(2):203-13. doi: 10.1007/s10522-011-9368-x. Epub 2011 Dec 6.
Telomeres are specialized structures designed to protect the ends of linear chromosomes. They are dynamic structures such that in normal somatic cells they constantly shorten as cell division progresses. There is compelling evidence that telomere shortening leads to cell senescence, a process perceived as the main cause of aging in higher mammals. Therefore, the features of telomere shortening are of great importance in understanding cell senescence and aging in general. By identifying unique subtelomeric regions, large enough to produce strong chemiluminescent signals, we have provided a new tool for Southern blot analysis of individual human Xp/Yp telomeres. We extend these results with quantitative fluorescence in situ hybridization using peptide nucleic acid probe (PNA Q-FISH) analysis of telomeres on the Y chromosome. Our results demonstrates unequal shortening dynamics between the p and q telomeres.
端粒是一种专门设计的结构,用于保护线性染色体的末端。它们是动态结构,因此在正常的体细胞中,随着细胞分裂的进行,端粒会不断缩短。有确凿的证据表明,端粒缩短会导致细胞衰老,这一过程被认为是高等哺乳动物衰老的主要原因。因此,端粒缩短的特征对于理解细胞衰老和衰老过程具有重要意义。通过鉴定足够大的独特亚端粒区域,我们为单个人类 Xp/Yp 端粒的 Southern 印迹分析提供了一种新工具。我们使用肽核酸探针(PNA Q-FISH)对 Y 染色体上的端粒进行定量荧光原位杂交,扩展了这些结果。我们的结果表明,p 和 q 端粒之间的缩短动态是不平衡的。