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通过转录因子 CEBPB 中磷酸开关的分歧进行调控进化。

Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB.

机构信息

Yale Systems Biology Institute and Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut 06511, USA.

出版信息

Nature. 2011 Nov 13;480(7377):383-6. doi: 10.1038/nature10595.

Abstract

There is an emerging consensus that gene regulation evolves through changes in cis-regulatory elements and transcription factors. Although it is clear how nucleotide substitutions in cis-regulatory elements affect gene expression, it is not clear how amino-acid substitutions in transcription factors influence gene regulation. Here we show that amino-acid changes in the transcription factor CCAAT/enhancer binding protein-β (CEBPB, also known as C/EBP-β) in the stem-lineage of placental mammals changed the way it responds to cyclic AMP/protein kinase A (cAMP/PKA) signalling. By functionally analysing resurrected ancestral proteins, we identify three amino-acid substitutions in an internal regulatory domain of CEBPB that are responsible for the novel function. These amino-acid substitutions reorganize the location of key phosphorylation sites, introducing a new site and removing two ancestral sites, reversing the response of CEBPB to GSK-3β-mediated phosphorylation from repression to activation. We conclude that changing the response of transcription factors to signalling pathways can be an important mechanism of gene regulatory evolution.

摘要

人们越来越认为,基因调控是通过顺式调控元件和转录因子的变化而进化的。虽然核苷酸取代如何影响顺式调控元件的基因表达是清楚的,但氨基酸取代如何影响转录因子的基因调控还不清楚。在这里,我们展示了胎盘哺乳动物谱系中转录因子 CCAAT/增强子结合蛋白-β(CEBPB,也称为 C/EBP-β)的氨基酸变化改变了它对环腺苷酸/蛋白激酶 A(cAMP/PKA)信号的反应方式。通过对复活的祖先蛋白进行功能分析,我们确定了 CEBPB 内部调节域中三个负责新功能的氨基酸取代。这些氨基酸取代重新组织了关键磷酸化位点的位置,引入了一个新的位点并去除了两个祖先位点,从而使 CEBPB 对 GSK-3β 介导的磷酸化的反应从抑制变为激活。我们得出结论,改变转录因子对信号通路的反应可以是基因调控进化的一个重要机制。

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