Expansion and contraction of ribosomal DNA repeats in Saccharomyces cerevisiae:: requirement of replication fork blocking (Fob1) protein and the role of RNA polymerase I

被引:320
|
作者
Kobayashi, T
Heck, DJ
Nomura, M
Horiuchi, T
机构
[1] Natl Inst Basic Biol, Okazaki, Aichi 4448585, Japan
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
关键词
replication fork blocking; RNA polymerase I; gene amplification; recombination hot spot; ribosomal DNA; sequence homogenization;
D O I
10.1101/gad.12.24.3821
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Saccharomyces cerevisiae carries similar to 150 copies of rDNA in tandem repeats. It was found that the absence of an essential subunit of RNA polymerase I (Pol I) in rpa135 deletion mutants triggers a gradual decrease in rDNA repeat number to about one-half the normal level. Reintroduction of the missing RPA135 gene induced a gradual increase in repeat number back to the normal level. Gene FOB1 was shown to be essential for both the decrease and increase of rDNA repeats. FOB1 was shown previously to be required for replication fork blocking (RFB) activity at RFB site in rDNA and for recombination hot-spot (HOT1) activity. Thus, DNA replication fork blockage appears to stimulate recombination and play an essential role in rDNA expansion/contraction and sequence homogenization, and possibly, in the instability of repeated sequences in general. RNA Pol I, on the other hand, appears to control repeat numbers, perhaps by stabilizing rDNA with the normal repeat numbers as a stable nucleolar structure.
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收藏
页码:3821 / 3830
页数:10
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