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酿酒酵母G1/S转录程序中,MluI细胞周期盒结合因子与Swi4/6细胞周期盒结合因子之间存在高度功能重叠。

High functional overlap between MluI cell-cycle box binding factor and Swi4/6 cell-cycle box binding factor in the G1/S transcriptional program in Saccharomyces cerevisiae.

作者信息

Bean James M, Siggia Eric D, Cross Frederick R

机构信息

Rockefeller University, New York, New York 10021, USA.

出版信息

Genetics. 2005 Sep;171(1):49-61. doi: 10.1534/genetics.105.044560. Epub 2005 Jun 18.

Abstract

In budding yeast, many genes are induced early in the cell cycle. Induction of these genes has been predominantly attributed to two transcription factors, Swi4-Swi6 (SBF) and Mbp1-Swi6 (MBF). Swi4 and Mbp1 are related DNA-binding proteins with dissimilar target sequences. For most G1/S-regulated genes that we tested in a cdc20 block-release protocol for cell-cycle synchronization, removal of both Swi4 and Mbp1 was necessary and sufficient to essentially eliminate cell-cycle-regulated expression. Detectable SBF or MBF binding sites (SCBs or MCBs) in the promoters or available genome-wide promoter occupancy data do not consistently explain this functional overlap. The overlapping ability of these transcription factors to regulate many promoters with very similar cell-cycle kinetics may provide robustness to the G1/S transcriptional response, but poses a puzzle with respect to promoter-transcription factor specificity. In addition, for some genes, deletion of Mbp1 or Swi4 enhances transcription, suggesting that these factors can also function as transcriptional repressors. Finally, we observe residual G1/S transcriptional regulation in the absence of Swi4 and Mbp1.

摘要

在出芽酵母中,许多基因在细胞周期早期被诱导。这些基因的诱导主要归因于两种转录因子,Swi4-Swi6(SBF)和Mbp1-Swi6(MBF)。Swi4和Mbp1是具有不同靶序列的相关DNA结合蛋白。对于我们在用于细胞周期同步的cdc20阻断-释放实验方案中测试的大多数G1/S调控基因,去除Swi4和Mbp1对于基本消除细胞周期调控的表达而言是必要且充分的。启动子中可检测到的SBF或MBF结合位点(SCBs或MCBs)或全基因组可用的启动子占据数据并不能始终如一地解释这种功能重叠。这些转录因子以非常相似的细胞周期动力学调控许多启动子的重叠能力可能为G1/S转录反应提供稳健性,但在启动子-转录因子特异性方面构成了一个难题。此外,对于一些基因,Mbp1或Swi4的缺失会增强转录,这表明这些因子也可以作为转录抑制因子发挥作用。最后,我们观察到在没有Swi4和Mbp1的情况下仍存在残余的G1/S转录调控。

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