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假菌丝生长过程中的转录因子调控与染色体动态变化

Transcription factor regulation and chromosome dynamics during pseudohyphal growth.

作者信息

Mayhew David, Mitra Robi D

机构信息

Department of Genetics and Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63108.

Department of Genetics and Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63108

出版信息

Mol Biol Cell. 2014 Sep 1;25(17):2669-76. doi: 10.1091/mbc.E14-04-0871. Epub 2014 Jul 9.

Abstract

Pseudohyphal growth is a developmental pathway seen in some strains of yeast in which cells form multicellular filaments in response to environmental stresses. We used multiplexed transposon "Calling Cards" to record the genome-wide binding patterns of 28 transcription factors (TFs) in nitrogen-starved yeast. We identified TF targets relevant for pseudohyphal growth, producing a detailed map of its regulatory network. Using tools from graph theory, we identified 14 TFs that lie at the center of this network, including Flo8, Mss11, and Mfg1, which bind as a complex. Surprisingly, the DNA-binding preferences for these key TFs were unknown. Using Calling Card data, we predicted the in vivo DNA-binding motif for the Flo8-Mss11-Mfg1 complex and validated it using a reporter assay. We found that this complex binds several important targets, including FLO11, at both their promoter and termination sequences. We demonstrated that this binding pattern is the result of DNA looping, which regulates the transcription of these targets and is stabilized by an interaction with the nuclear pore complex. This looping provides yeast cells with a transcriptional memory, enabling them more rapidly to execute the filamentous growth program when nitrogen starved if they had been previously exposed to this condition.

摘要

假菌丝生长是在某些酵母菌株中观察到的一种发育途径,其中细胞在环境压力下形成多细胞丝状体。我们使用多重转座子“呼叫卡”来记录氮饥饿酵母中28种转录因子(TFs)的全基因组结合模式。我们确定了与假菌丝生长相关的TF靶点,绘制了其调控网络的详细图谱。使用图论工具,我们确定了位于该网络中心的14种TFs,包括作为复合物结合的Flo8、Mss11和Mfg1。令人惊讶的是,这些关键TFs的DNA结合偏好尚不清楚。利用呼叫卡数据,我们预测了Flo8-Mss11-Mfg1复合物的体内DNA结合基序,并使用报告基因检测进行了验证。我们发现该复合物在几个重要靶点的启动子和终止序列处均有结合,包括FLO11。我们证明这种结合模式是DNA环化的结果,DNA环化调节这些靶点的转录,并通过与核孔复合物的相互作用而稳定。这种环化为酵母细胞提供了一种转录记忆,使它们在先前暴露于氮饥饿条件下时,如果再次处于氮饥饿状态,能够更迅速地执行丝状生长程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ac/4148256/5e0cbb760d80/2669fig1.jpg

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