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裂殖酵母中DSC1组分cdc10+、rep1+和rep2+在有丝分裂G1-S边界处对MCB基因转录的作用。

The role of DSC1 components cdc10+, rep1+ and rep2+ in MCB gene transcription at the mitotic G1-S boundary in fission yeast.

作者信息

White S, Khaliq F, Sotiriou S, McInerny C J

机构信息

Division of Biochemistry and Molecular Biology, Institute of Biological and Life Sciences, University of Glasgow, UK.

出版信息

Curr Genet. 2001 Dec;40(4):251-9. doi: 10.1007/s002940100248.

Abstract

In this paper, we describe the transcription profile of a group of genes at the G1-S boundary of fission yeast in synchronously dividing mitotic cells, under a variety of different conditions. This transcription profile is unaffected in cells where either cdc10+ or cdc10-C4 are constitutively overexpressed. In contrast, overexpression of either rep1+ or rep2+ results in constitutive expression of MCB-regulated genes, suggesting that these polypeptides have important regulatory properties in controlling MCB transcription. Finally, we examine the pattern of MCB-regulated transcription in cells where the G1 period is extended. Surprisingly, we find that the wee1-50 mutation causes MCB transcription throughout the cell cycle, whereas cells re-fed after nitrogen starvation have normal expression patterns. The implications of these observations for understanding MCB-regulated transcription are discussed.

摘要

在本文中,我们描述了在多种不同条件下,同步分裂的有丝分裂细胞中裂殖酵母G1-S边界处一组基因的转录谱。在持续过表达cdc10+或cdc10-C4的细胞中,这种转录谱不受影响。相比之下,rep1+或rep2+的过表达导致MCB调控基因的组成型表达,这表明这些多肽在控制MCB转录方面具有重要的调控特性。最后,我们研究了G1期延长的细胞中MCB调控转录的模式。令人惊讶的是,我们发现wee1-50突变导致整个细胞周期的MCB转录,而氮饥饿后重新喂食的细胞具有正常的表达模式。讨论了这些观察结果对理解MCB调控转录的意义。

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