Bermejo Rodrigo, Capra Thelma, Gonzalez-Huici Victor, Fachinetti Daniele, Cocito Andrea, Natoli Gioacchino, Katou Yuki, Mori Hiroshi, Kurokawa Ken, Shirahige Katsuhiko, Foiani Marco
Fondazione IFOM Istituto FIRC di Oncologia Moleculare (IFOM-IEO Campus), Via Adamello 16, 20139 Milan, Italy.
Cell. 2009 Sep 4;138(5):870-84. doi: 10.1016/j.cell.2009.06.022.
Specialized topoisomerases solve the topological constraints arising when replication forks encounter transcription. We have investigated the contribution of Top2 in S phase transcription. Specifically in S phase, Top2 binds intergenic regions close to transcribed genes. The Top2-bound loci exhibit low nucleosome density and accumulate gammaH2A when Top2 is defective. These intergenic loci associate with the HMG protein Hmo1 throughout the cell cycle and are refractory to the histone variant Htz1. In top2 mutants, Hmo1 is deleterious and accumulates at pericentromeric regions in G2/M. Our data indicate that Top2 is dispensable for transcription and that Hmo1 and Top2 bind in the proximity of genes transcribed in S phase suppressing chromosome fragility at the M-G1 transition. We propose that an Hmo1-dependent epigenetic signature together with Top2 mediate an S phase architectural pathway to preserve genome integrity.
专门的拓扑异构酶解决了复制叉遇到转录时出现的拓扑限制问题。我们研究了Top2在S期转录中的作用。具体而言,在S期,Top2结合于靠近转录基因的基因间区域。当Top2有缺陷时,与Top2结合的位点表现出低核小体密度并积累γH2A。这些基因间位点在整个细胞周期中都与HMG蛋白Hmo1相关联,并且对组蛋白变体Htz1具有抗性。在top2突变体中,Hmo1是有害的,并在G2/M期在着丝粒周围区域积累。我们的数据表明,Top2对于转录是可有可无的,并且Hmo1和Top2在S期转录的基因附近结合,从而在M-G1转换时抑制染色体脆弱性。我们提出,一种依赖于Hmo1的表观遗传特征与Top2一起介导了一条S期结构途径以维持基因组完整性。