Sfeir Agnel J, Chai Weihang, Shay Jerry W, Wright Woodring E
Department of Cell Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA.
Mol Cell. 2005 Apr 1;18(1):131-8. doi: 10.1016/j.molcel.2005.02.035.
Mammalian telomeres end in single-stranded, G-rich 3' overhangs resulting from both the "end-replication problem" (the inability of DNA polymerase to replicate the very end of the telomeres) and postreplication processing. Telomeric G-rich overhangs are precisely defined in ciliates; the length and the terminal nucleotides are fixed. Human telomeres have very long overhangs that are heterogeneous in size (35-600 nt), indicating that their processing must differ in some respects from model organisms. We developed telomere-end ligation protocols that allowed us to identify the terminal nucleotides of both the C-rich and the G-rich telomere strands. Up to approximately 80% of the C-rich strands terminate in CCAATC-5', suggesting that after replication a nuclease with high specificity or constrained action acts on the C strand. In contrast, the G-terminal nucleotide was less precise than Tetrahymena and Euplotes but still had a bias that changed as a function of telomerase expression.
哺乳动物的端粒以单链、富含G的3'端悬突结尾,这是由“末端复制问题”(DNA聚合酶无法复制端粒的最末端)和复制后加工导致的。在纤毛虫中,富含G的端粒悬突被精确界定;其长度和末端核苷酸是固定的。人类端粒具有非常长的悬突,其大小是异质的(35 - 600个核苷酸),这表明它们的加工在某些方面一定与模式生物不同。我们开发了端粒末端连接方案,使我们能够鉴定富含C和富含G的端粒链的末端核苷酸。高达约80%的富含C的链以CCAATC - 5'结尾,这表明复制后一种具有高特异性或受限作用的核酸酶作用于C链。相比之下,G末端核苷酸不如嗜热四膜虫和游仆虫精确,但仍存在一种随端粒酶表达而变化的偏向性。