Cell cycle regulated expression of the WHI7 Start repressor gene.

IF 3.4 3区 生物学 Q3 CELL BIOLOGY Cell Cycle Pub Date : 2024-09-16 DOI:10.1080/15384101.2024.2402192
Cristina Ros-Carrero, Mercè Gomar-Alba, J Carlos Igual
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Abstract

Periodic transcriptional waves along the cell cycle ensure the accurate progression of the different cell cycle phases through the timely regulated expression of cell cycle proteins. The G1/S transition (Start) consists in the activation of a transcriptional program by G1 CDKs through the inactivation of Start transcriptional repressors, Whi5 and Whi7 in yeast or Rb in mammals. Here, we provide a comprehensive characterization of the transcriptional regulation of the Start repressor Whi7 in budding yeast. We found that WHI7 is a cell cycle regulated gene that shows periodic expression peaking in G1. Our results demonstrate that the three cell cycle transcriptional programs related to G1 and their corresponding transcription factors are involved in the transcriptional control of WHI7. Specifically, we identified that the transcriptional regulators Swi5 and Mcm1-Yox1, which are involved in late M and early G1 expression, and the transcription factors MBF and SBF, which are responsible for G1/S expression, are able to associate and regulate the WHI7 gene. In summary, in this work, we provide new mechanisms for the regulation of the Start repressor Whi7, which highlights the precise and complex control of the cell cycle machinery governing the G1/S transition.

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细胞周期调控 WHI7 启动抑制基因的表达。
细胞周期中的周期性转录波通过及时调控细胞周期蛋白的表达,确保不同细胞周期阶段的准确进展。G1/S转变(Start)是由G1 CDK通过Start转录抑制因子(酵母中的Whi5和Whi7或哺乳动物中的Rb)的失活激活转录程序。在这里,我们对芽殖酵母中Start转录抑制因子Whi7的转录调控进行了全面描述。我们发现,WHI7 是一个细胞周期调控基因,在 G1 期表现出周期性的表达高峰。我们的研究结果表明,与G1相关的三个细胞周期转录程序及其相应的转录因子参与了WHI7的转录调控。具体来说,我们发现参与M后期和G1早期表达的转录调节因子Swi5和Mcm1-Yox1,以及负责G1/S表达的转录因子MBF和SBF能够联合调控WHI7基因。总之,在这项工作中,我们提供了起始抑制因子Whi7的新调控机制,凸显了细胞周期机制对G1/S转换的精确而复杂的调控。
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来源期刊
Cell Cycle
Cell Cycle 生物-细胞生物学
CiteScore
7.70
自引率
2.30%
发文量
281
审稿时长
1 months
期刊介绍: Cell Cycle is a bi-weekly peer-reviewed journal of high priority research from all areas of cell biology. Cell Cycle covers all topics from yeast to man, from DNA to function, from development to aging, from stem cells to cell senescence, from metabolism to cell death, from cancer to neurobiology, from molecular biology to therapeutics. Our goal is fast publication of outstanding research.
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