Hmo1, an HMG-box protein, belongs to the yeast ribosomal DNA transcription system

被引:91
作者
Gadal, O
Labarre, S
Boschiero, C
Thuriaux, P
机构
[1] CEA Saclay, Serv Biochim & Genet Mol, Lab Physiogenom, F-91191 Gif Sur Yvette, France
[2] Inst Pasteur, Lab Biol Cellulaire Noyau, F-75724 Paris 15, France
关键词
nucleolus; RNA polymerase I; SGS1; topoisomerases; UBF;
D O I
10.1093/emboj/cdf539
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
Hmo1 is one of seven HMG-box proteins of Saccharomyces cerevisiae. Null mutants have a limited effect on growth. Hmo1 overexpression suppresses rpa49-Delta mutants lacking Rpa49, a non-essential but conserved subunit of RNA polymerase I corresponding to the animal RNA polymerase I factor PAF53. This overexpression strongly increases de novo rRNA synthesis. rpa49-Delta hmo1-Delta double mutants are lethal, and this lethality is bypassed when RNA polymerase 11 synthesizes rRNA. Hmo1 co-localizes with Fob1, a known rDNA-binding protein, defining a narrow territory adjacent to the nucleoplasm that could delineate the rDNA nucleolar domain. These data identify Hmo1 as a genuine RNA polymerase I factor acting synergistically with Rpa49. As an HMG-box protein, Hmo1 is remotely related to animal UBF factors. hmo1-Delta and rpa49-Delta are lethal with top3-Delta DNA topoisomerase (type 1) mutants and are suppressed in mutants lacking the Sgs1 DNA helicase. They are not affected by top1-Delta defective in Top1, the other eukaryotic type I topoisomerase. Conversely, rpa34-Delta mutants lacking Rpa34, a non-essential subunit associated with Rpa49, are lethal in top1-Delta but not in top3-Delta.
引用
收藏
页码:5498 / 5507
页数:10
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