酵母端粒区域DNA复制叉移动的解剖学与动力学
Anatomy and dynamics of DNA replication fork movement in yeast telomeric regions.
作者信息
Makovets Svetlana, Herskowitz Ira, Blackburn Elizabeth H
机构信息
University of California, San Francisco, Department of Biochemistry and Biophysics, San Francisco, California 94143-2200,USA.
出版信息
Mol Cell Biol. 2004 May;24(9):4019-31. doi: 10.1128/MCB.24.9.4019-4031.2004.
Replication initiation and replication fork movement in the subtelomeric and telomeric DNA of native Y' telomeres of yeast were analyzed using two-dimensional gel electrophoresis techniques. Replication origins (ARSs) at internal Y' elements were found to fire in early-mid-S phase, while ARSs at the terminal Y' elements were confirmed to fire late. An unfired Y' ARS, an inserted foreign (bacterial) sequence, and, as previously reported, telomeric DNA each were shown to impose a replication fork pause, and pausing is relieved by the Rrm3p helicase. The pause at telomeric sequence TG(1-3) repeats was stronger at the terminal tract than at the internal TG(1-3) sequences located between tandem Y' elements. We show that the telomeric replication fork pause associated with the terminal TG(1-3) tracts begins approximately 100 bp upstream of the telomeric repeat tract sequence. Telomeric pause strength was dependent upon telomere length per se and did not require the presence of a variety of factors implicated in telomere metabolism and/or known to cause telomere shortening. The telomeric replication fork pause was specific to yeast telomeric sequence and was independent of the Sir and Rif proteins, major known components of yeast telomeric heterochromatin.
利用二维凝胶电泳技术分析了酵母天然Y'端粒的亚端粒和端粒DNA中的复制起始和复制叉移动情况。发现内部Y'元件处的复制起点(ARSs)在S期早期至中期激活,而末端Y'元件处的ARSs则在晚期激活。一个未激活的Y' ARS、一个插入的外源(细菌)序列,以及如先前报道的端粒DNA,均显示会导致复制叉停顿,而Rrm3p解旋酶可缓解这种停顿。端粒序列TG(1-3)重复序列处的停顿在末端片段比串联Y'元件之间的内部TG(1-3)序列处更强。我们发现,与末端TG(1-3)片段相关的端粒复制叉停顿始于端粒重复序列上游约100 bp处。端粒停顿强度取决于端粒本身的长度,并且不需要多种参与端粒代谢和/或已知会导致端粒缩短的因子的存在。端粒复制叉停顿对酵母端粒序列具有特异性,并且独立于Sir和Rif蛋白,这两种蛋白是酵母端粒异染色质的主要已知成分。