Highly Transcribed RNA Polymerase II Genes Are Impediments to Replication Fork Progression in Saccharomyces cerevisiae

被引:233
作者
Azvolinsky, Anna [3 ]
Giresi, Paul G. [1 ,2 ]
Lieb, Jason D. [1 ,2 ]
Zakian, Virginia A. [3 ]
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Carolina Ctr Genome Sci, Chapel Hill, NC 27599 USA
[3] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
DNA-REPLICATION; RIBOSOMAL DNA; HELICASE RRM3P; FRAGILE SITES; YEAST GENOME; PROTEIN; RECOMBINATION; MAINTENANCE; INSTABILITY; MECHANISMS;
D O I
10.1016/j.molcel.2009.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Replication forks face multiple obstacles that slow their progression. By two-dimensional gel analysis, yeast forks pause at stable DNA protein complexes, and this pausing is greatly increased in the absence of the Rrm3 helicase. We used a genome-wide approach to identify 96 sites of very high DNA polymerase binding in wild-type cells. Most of these binding sites were not previously identified pause sites. Rather, the most highly represented genomic category among high DNA polymerase binding sites was the open reading frames (ORFs) of highly transcribed RNA polymerase II genes. Twice as many pause sites were identified in rrm3 compared with wild-type cells, as pausing in this strain occurred at both highly transcribed RNA polymerase II genes and the previously identified protein DNA complexes. ORFs of highly transcribed RNA polymerase II genes are a class of natural pause sites that are not exacerbated in rrm3 cells.
引用
收藏
页码:722 / 734
页数:13
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