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The Reconstruction of Condition-Specific Transcriptional Modules Provides New Insights in the Evolution of Yeast AP-1 Proteins

机译:条件特定转录模块的重建为酵母AP-1蛋白的进化提供了新的见解。

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摘要

AP-1 proteins are transcription factors (TFs) that belong to the basic leucine zipper family, one of the largest families of TFs in eukaryotic cells. Despite high homology between their DNA binding domains, these proteins are able to recognize diverse DNA motifs. In yeasts, these motifs are referred as YRE (Yap Response Element) and are either seven (YRE-Overlap) or eight (YRE-Adjacent) base pair long. It has been proposed that the AP-1 DNA binding motif preference relies on a single change in the amino acid sequence of the yeast AP-1 TFs (an arginine in the YRE-O binding factors being replaced by a lysine in the YRE-A binding Yaps). We developed a computational approach to infer condition-specific transcriptional modules associated to the orthologous AP-1 protein Yap1p, Cgap1p and Cap1p, in three yeast species: the model yeast Saccharomyces cerevisiae and two pathogenic species Candida glabrata and Candida albicans. Exploitation of these modules in terms of predictions of the protein/DNA regulatory interactions changed our vision of AP-1 protein evolution. Cis-regulatory motif analyses revealed the presence of a conserved adenine in 5′ position of the canonical YRE sites. While Yap1p, Cgap1p and Cap1p shared a remarkably low number of target genes, an impressive conservation was observed in the YRE sequences identified by Yap1p and Cap1p. In Candida glabrata, we found that Cgap1p, unlike Yap1p and Cap1p, recognizes YRE-O and YRE-A motifs. These findings were supported by structural data available for the transcription factor Pap1p (Schizosaccharomyces pombe). Thus, whereas arginine and lysine substitutions in Cgap1p and Yap1p proteins were reported as responsible for a specific YRE-O or YRE-A preference, our analyses rather suggest that the ancestral yeast AP-1 protein could recognize both YRE-O and YRE-A motifs and that the arginine/lysine exchange is not the only determinant of the specialization of modern Yaps for one motif or another.
机译:AP-1蛋白是属于基本亮氨酸拉链家族的转录因子(TFs),该家族是真核细胞中最大的TFs家族之一。尽管它们的DNA结合结构域之间具有高度同源性,但这些蛋白质仍能够识别各种DNA图案。在酵母中,这些基序称为YRE(Yap响应元件),长度为7个(YRE重叠)或8个(YRE相邻)碱基对。已经提出,AP-1 DNA结合基序偏好性取决于酵母AP-1 TFs的氨基酸序列的单一变化(YRE-O结合因子中的精氨酸被YRE-A中的赖氨酸替代)绑定的Yaps)。我们开发了一种计算方法来推断与以下三种酵母物种中的直系同源AP-1蛋白Yap1p,Cgap1p和Cap1p相关的条件特异性转录模块:模型酵母酿酒酵母和两种病原种光滑念珠菌和白色念珠菌。利用这些模块预测蛋白质/ DNA调控相互作用,改变了我们对AP-1蛋白质进化的认识。顺式调控基序分析表明,在典型的YRE位点的5'位置存在保守的腺嘌呤。虽然Yap1p,Cgap1p和Cap1p共享极少的靶基因,但在Yap1p和Cap1p鉴定的YRE序列中观察到了惊人的保守性。在光滑念珠菌中,我们发现Cgap1p与Yap1p和Cap1p不同,可识别YRE-O和YRE-A图案。这些发现得到了转录因子Pap1p(Schizosaccharomyces pombe)可用结构数据的支持。因此,虽然据报道Cgap1p和Yap1p蛋白中的精氨酸和赖氨酸取代是造成特定YRE-O或YRE-A偏好的原因,但我们的分析表明,祖先的酵母AP-1蛋白可以识别YRE-O和YRE-A。且精氨酸/赖氨酸的交换不是现代Yaps专业化一个或另一个主题的唯一决定因素。

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