首页> 美国卫生研究院文献>Cell Regulation >Genome-wide Expression Profiling In Vivo DNA Binding Analysis and Probabilistic Motif Prediction Reveal Novel Abf1 Target Genes during Fermentation Respiration and Sporulation in Yeast
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Genome-wide Expression Profiling In Vivo DNA Binding Analysis and Probabilistic Motif Prediction Reveal Novel Abf1 Target Genes during Fermentation Respiration and Sporulation in Yeast

机译:全基因组表达谱体内DNA结合分析和概率母题预测揭示了酵母发酵呼吸和孢子形成过程中的新型Abf1目标基因。

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摘要

The autonomously replicating sequence binding factor 1 (Abf1) was initially identified as an essential DNA replication factor and later shown to be a component of the regulatory network controlling mitotic and meiotic cell cycle progression in budding yeast. The protein is thought to exert its functions via specific interaction with its target site as part of distinct protein complexes, but its roles during mitotic growth and meiotic development are only partially understood. Here, we report a comprehensive approach aiming at the identification of direct Abf1-target genes expressed during fermentation, respiration, and sporulation. Computational prediction of the protein's target sites was integrated with a genome-wide DNA binding assay in growing and sporulating cells. The resulting data were combined with the output of expression profiling studies using wild-type versus temperature-sensitive alleles. This work identified 434 protein-coding loci as being transcriptionally dependent on Abf1. More than 60% of their putative promoter regions contained a computationally predicted Abf1 binding site and/or were bound by Abf1 in vivo, identifying them as direct targets. The present study revealed numerous loci previously unknown to be under Abf1 control, and it yielded evidence for the protein's variable DNA binding pattern during mitotic growth and meiotic development.
机译:自主复制序列结合因子1(Abf1)最初被鉴定为必需的DNA复制因子,后来被证明是控制发芽酵母中有丝分裂和减数分裂细胞周期进程的调控网络的组成部分。人们认为该蛋白质通过与靶位点的特异性相互作用来发挥其功能,而这种靶位点是不同蛋白质复合物的一部分,但在有丝分裂生长和减数分裂发育过程中的作用仅得到部分了解。在这里,我们报告了一种旨在鉴定在发酵,呼吸和孢子形成过程中表达的直接Abf1目标基因的综合方法。在生长和孢子形成细胞中,将蛋白质靶位点的计算预测与全基因组DNA结合测定相结合。使用野生型对温度敏感的等位基因,将所得数据与表达谱研究的输出相结合。这项工作确定了434个蛋白质编码基因座在转录上依赖于Abf1。他们超过60%的推定启动子区域包含一个计算预测的Abf1结合位点和/或在体内被Abf1结合,从而将它们鉴定为直接靶标。本研究揭示了许多以前未知的基因位点在Abf1的控制下,它为有丝分裂生长和减数分裂发育过程中蛋白质可变的DNA结合模式提供了证据。

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