Gadal Olivier, Labarre Sylvie, Boschiero Claire, Thuriaux Pierre
Laboratoire de Physio-Génomique, Service de Biochimie et Génétique Moléculaire, CEA/Saclay, Bâtiment 142, F-91191 Gif-sur-Yvette, France.
EMBO J. 2002 Oct 15;21(20):5498-507. doi: 10.1093/emboj/cdf539.
Hmo1 is one of seven HMG-box proteins of Saccharo myces 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 II 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 I) 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.
Hmo1是酿酒酵母七种HMG盒蛋白之一。缺失突变体对生长的影响有限。Hmo1的过表达可抑制缺乏Rpa49的rpa49-Δ突变体,Rpa49是RNA聚合酶I的一个非必需但保守的亚基,对应于动物RNA聚合酶I因子PAF53。这种过表达强烈增加了从头rRNA合成。rpa49-Δ hmo1-Δ双突变体是致死的,当RNA聚合酶II合成rRNA时,这种致死性被绕过。Hmo1与Fob1(一种已知的rDNA结合蛋白)共定位,定义了一个与核质相邻的狭窄区域,该区域可能划定rDNA核仁结构域。这些数据确定Hmo1是一种与Rpa49协同作用的真正的RNA聚合酶I因子。作为一种HMG盒蛋白,Hmo1与动物UBF因子有较远的亲缘关系。hmo1-Δ和rpa49-Δ与top3-Δ DNA拓扑异构酶(I型)突变体是致死的,并且在缺乏Sgs1 DNA解旋酶的突变体中被抑制。它们不受另一种真核I型拓扑异构酶Top1缺陷的top1-Δ的影响。相反,缺乏与Rpa49相关的非必需亚基Rpa34的rpa34-Δ突变体在top1-Δ中是致死的,但在top3-Δ中不是。