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Key Function for the CCAAT-Binding Factor Php4 To Regulate Gene Expression in Response to Iron Deficiency in Fission Yeast

机译:CCAAT结合因子Php4调节裂变酵母对缺铁反应的基因表达的关键功能

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The fission yeast Schizosaccharomyces pombe responds to the deprivation of iron by inducing the expression of the php4+ gene, which encodes a negative regulatory subunit of the heteromeric CCAAT-binding factor. Once formed, the Php2/3/4/5 transcription complex is required to inactivate a subset of genes encoding iron-using proteins. Here, we used a pan-S. pombe microarray to study the transcriptional response to iron starvation and identified 86 genes that exhibit php4+-dependent changes on a genome-wide scale. One of these genes encodes the iron-responsive transcriptional repressor Fep1, whose mRNA levels were decreased after treatment with the permeant iron chelator 2,2′-dipyridyl. In addition, several genes encoding the components of iron-dependent biochemical pathways, including the tricarboxylic acid cycle, mitochondrial respiration, amino acid biosynthesis, and oxidative stress defense, were downregulated in response to iron deficiency. Furthermore, Php4 repressed transcription when brought to a promoter using a yeast DNA-binding domain, and iron deprivation was required for this repression. On the other hand, Php4 was constitutively active when glutathione levels were depleted within the cell. Based on these and previous results, we propose that iron-dependent inactivation of Php4 is regulated at two distinct levels: first, at the transcriptional level by the iron-responsive GATA factor Fep1 and second, at the posttranscriptional level by a mechanism yet to be identified, which inhibits Php4-mediated repressive function when iron is abundant.
机译:裂变酵母 Schizosaccharomyces pombe 通过诱导 php4 + 基因的表达来响应铁的缺乏。编码异聚CCAAT结合因子的负调节亚基。一旦形成,需要Php2 / 3/4/5转录复合物来灭活编码铁蛋白的基因的子集。在这里,我们使用了pan-em。 pombe 基因芯片研究铁饥饿的转录反应,鉴定出86个基因,这些基因在基因组上表现出 php4 + 依赖性变化。大规模。这些基因之一编码铁反应性转录抑制因子Fep1,在用渗透性铁螯合剂2,2'-联吡啶处理后,其mRNA水平降低。此外,响应铁缺乏症,一些编码铁依赖性生化途径组成部分的基因被下调,包括三羧酸循环,线粒体呼吸,氨基酸生物合成和氧化应激防御。此外,当使用酵母DNA结合结构域将Php4带入启动子时,它会抑制转录,因此这种抑制作用需要铁的剥夺。另一方面,当细胞内的谷胱甘肽水平耗尽时,Php4具有组成型活性。根据这些结果和以前的结果,我们建议铁依赖性的Php4失活在两个不同的水平上调节:首先,在转录水平上受铁反应性GATA因子Fep1的调节,其次在转录后水平上的调节机制尚待研究。鉴定出,当铁丰富时,它可以抑制Php4介导的抑制功能。

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