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裂殖酵母中 Mid1p 依赖的 M-G1 转录波的调控。

Mid1p-dependent regulation of the M-G1 transcription wave in fission yeast.

机构信息

Division of Molecular and Cellular Biology, Faculty of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.

出版信息

J Cell Sci. 2010 Dec 15;123(Pt 24):4366-73. doi: 10.1242/jcs.073049. Epub 2010 Nov 23.

Abstract

The control of gene expression at certain times during the mitotic cell division cycle is a common feature in eukaryotes. In fission yeast, at least five waves of gene expression have been described, with one transcribed at the M-G1 interval under the control of the PBF transcription factor complex. PBF consists of at least three transcription factors, two forkhead-like proteins Sep1p and Fkh2p, and a MADS box-like protein Mbx1p, and binds to PCB motifs found in the gene promoters. Mbx1p is under the direct control of the polo-like kinase Plo1p and the Cdc14p-like phosphatase Clp1p (Flp1p). Here, we show that M-G1 gene expression in fission yeast is also regulated by the anillin-like protein, Mid1p (Dmf1p). Mid1p binds in vivo to both Fkh2p and Sep1p, and to the promoter regions of M-G1 transcribed genes. Mid1p promoter binding is dependent on Fkh2p, Plo1p and Clp1p. The absence of mid1(+) in cells results in partial loss of M-G1 specific gene expression, suggesting that it has a negative role in controlling gene expression. This phenotype is exacerbated by also removing clp1(+), suggesting that Mid1p and Clp1p have overlapping functions in controlling transcription. As mid1(+) is itself expressed at M-G1, these observations offer a new mechanism whereby Mid1p contributes to controlling cell cycle-specific gene expression as part of a feedback loop.

摘要

有丝分裂细胞周期特定时间的基因表达控制是真核生物的共同特征。在裂殖酵母中,已经描述了至少五波基因表达,其中一波在 PBF 转录因子复合物的控制下在 M-G1 间隔转录。PBF 至少由三个转录因子组成,两个叉头样蛋白 Sep1p 和 Fkh2p,以及一个 MADS 盒样蛋白 Mbx1p,并且与基因启动子中发现的 PCB 基序结合。Mbx1p 受 polo 样激酶 Plo1p 和 Cdc14p 样磷酸酶 Clp1p(Flp1p)的直接控制。在这里,我们表明裂殖酵母中的 M-G1 基因表达也受肌球蛋白样蛋白 Mid1p(Dmf1p)的调节。Mid1p 在体内与 Fkh2p 和 Sep1p 以及 M-G1 转录基因的启动子区域结合。Mid1p 启动子结合依赖于 Fkh2p、Plo1p 和 Clp1p。细胞中 mid1(+) 的缺失导致 M-G1 特异性基因表达部分丧失,表明它在控制基因表达中具有负作用。这种表型因同时去除 clp1(+) 而加剧,表明 Mid1p 和 Clp1p 在控制转录方面具有重叠功能。由于 mid1(+) 本身在 M-G1 时表达,这些观察结果提供了一种新的机制,即 Mid1p 作为反馈环的一部分,通过控制细胞周期特异性基因表达来发挥作用。

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