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首页> 外文期刊>Nucleic Acids Research >Fep1 represses expression of the fission yeast Schizosaccharomyces pombe siderophore-iron transport system
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Fep1 represses expression of the fission yeast Schizosaccharomyces pombe siderophore-iron transport system

机译:Fep1抑制裂变酵母粟酒裂殖酵母铁载体运输系统的表达

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When iron repletes, Schizosaccharomyces pombe cells repress transcription of genes encoding components involved in the reductive iron transport system. Fep1 mediates this transcriptional control by interacting specifically with GATA-type cis-acting elements. To further investigate the role that Fep1 plays in iron homeostasis, we searched for additional Fep1-regulated genes. We found that str1~+ is subject to negative transcriptional regulation, which is exerted through binding of Fep1 to a single GATA element in the str1~+ promoter. Introduction of str1~+ into a Saccharomyces cerevisiae fet3Δ arn1-4Δ strain led to assimilation of iron from ferrichrome, revealing that Str1 functions as a siderophore-iron transporter in S.pombe. We also identified two additional target genes of Fep1, named str2~+ and str3~+. We demonstrate that the str1~+, str2~ and str3~+ genes share a common promoter element, 5'-(A/T)GATAA-3'. We found that the N-terminal 241 residue segment of Fep1 expressed in Escherichia coli specifically interacts with the 5'-(A/T)GATAA-3' element present in each of these promoters. Consistent with this, constitutive high level str1~+, str2~+ and str3~+ gene expression was observed in a fep1Δ mutant strain. Taken together, these results demonstrate that Fep1 occupies a central role in coordinating transcriptional regulation of genes encoding components of the reductive and non-reductive iron transport systems in fission yeast.
机译:当铁补充时,粟酒裂殖酵母细胞会抑制编码与还原铁转运系统有关的成分的基因的转录。 Fep1通过与GATA型顺式作用元件特异性相互作用来介导这种转录控制。为了进一步研究Fep1在铁稳态中的作用,我们搜索了其他受Fep1调控的基因。我们发现str1〜+受到负转录调控,这是通过将Fep1与str1〜+启动子中的单个GATA元件结合而发挥的。将str1〜+引入酿酒酵母fet3Δarn1-4Δ菌株中导致铁与铬铁的同化,表明Str1在粟酒裂殖酵母中起着铁载体的作用。我们还鉴定了Fep1的另外两个靶基因,分别名为str2〜+和str3〜+。我们证明str1〜+,str2〜和str3〜+基因共享一个共同的启动子元件5'-(A / T)GATAA-3'。我们发现,在大肠杆菌中表达的Fep1的N端241残基片段与这些启动子中的5'-(A / T)GATAA-3'元件特异性相互作用。与此一致,在fep1Δ突变株中观察到组成型高水平str1〜+,str2〜+和str3〜+基因表达。综上,这些结果表明,Fep1在协调裂变酵母中编码还原性和非还原性铁转运系统成分的基因的转录调控中起着核心作用。

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