Shimanuki Mizuki, Chung Soo-Yoel, Chikashige Yuji, Kawasaki Yosuke, Uehara Lisa, Tsutsumi Chihiro, Hatanaka Mitsuko, Hiraoka Yasushi, Nagao Koji, Yanagida Mitsuhiro
Initial Research Project (IRP), Okinawa Institute of Science and Technology Promotion Corporation (OIST), Uruma 904-2234, Okinawa, Japan.
Genes Cells. 2007 May;12(5):677-92. doi: 10.1111/j.1365-2443.2007.01079.x.
Body cells in multicellular organisms are in the G0 state, in which cells are arrested and terminally differentiated. To understand how the G0 state is maintained, the genes that are specifically expressed or repressed in G0 must be identified, as they control G0. In the fission yeast Schizosaccharomyces pombe, haploid cells are completely arrested under nitrogen source starvation with high viability. We examined the global transcriptome of G0 cells and cells on the course to resume vegetative growth. Approximately 20% of the transcripts of approximately 5000 genes increased or decreased more than fourfold in the two-step transitions that occur prior to replication. Of the top 30 abundant transcripts in G0, 23 were replaced by ribosome- and translation-related transcripts in the dividing vegetative state. Eight identified clusters with distinct alteration patterns of approximately 2700 transcripts were annotated by Gene Ontology. Disruption of 53 genes indicated that nine of them were necessary to support the proper G0 state. These nine genes included two C2H2 zinc finger transcription factors, a cyclin-like protein implicated in phosphorylation of RNA polymerase II, two putative autophagy regulators, a G-protein activating factor, and two CBS domain proteins, possibly involved in AMP-activated kinase.
多细胞生物中的体细胞处于G0状态,在此状态下细胞停滞并终末分化。为了解G0状态是如何维持的,必须鉴定在G0中特异性表达或被抑制的基因,因为它们控制着G0。在裂殖酵母粟酒裂殖酵母中,单倍体细胞在氮源饥饿条件下完全停滞,且具有高活力。我们检测了G0细胞以及处于恢复营养生长过程中的细胞的整体转录组。在复制前发生的两步转变中,大约5000个基因的转录本中约20%增加或减少了四倍以上。在G0中丰度最高的30个转录本中,有23个在分裂的营养状态下被核糖体和翻译相关的转录本所取代。通过基因本体论对8个鉴定出的具有约2700个转录本不同变化模式的簇进行了注释。对53个基因的破坏表明其中9个基因对于维持适当的G0状态是必需的。这9个基因包括两个C2H2锌指转录因子、一个与RNA聚合酶II磷酸化有关的类细胞周期蛋白、两个假定的自噬调节因子、一个G蛋白激活因子以及两个可能参与AMP激活激酶的CBS结构域蛋白。