Alternative Oxidase Transcription Factors AOD2 and AOD5 of Neurospora crassa Control the Expression of Genes Involved in Energy Production and Metabolism.

Zhigang Qi, Kristina M Smith, Erin L Bredeweg, Natasa Bosnjak, Michael Freitag, Frank E Nargang
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Abstract

In Neurospora crassa, blocking the function of the standard mitochondrial electron transport chain results in the induction of an alternative oxidase (AOX). AOX transfers electrons directly from ubiquinol to molecular oxygen. AOX serves as a model of retrograde regulation since it is encoded by a nuclear gene that is regulated in response to signals from mitochondria. The N. crassa transcription factors AOD2 and AOD5 are necessary for the expression of the AOX gene. To gain insight into the mechanism by which these factors function, and to determine if they have roles in the expression of additional genes in N. crassa, we constructed strains expressing only tagged versions of the proteins. Cell fractionation experiments showed that both proteins are localized to the nucleus under both AOX inducing and noninducing conditions. Furthermore, chromatin immunoprecipitation and high throughput sequencing (ChIP-seq) analysis revealed that the proteins are bound to the promoter region of the AOX gene under both conditions. ChIP-seq also showed that the transcription factors bind to the upstream regions of a number of genes that are involved in energy production and metabolism. Dependence on AOD2 and AOD5 for the expression of several of these genes was verified by quantitative PCR. The majority of ChIP-seq peaks observed were enriched for both AOD2 and AOD5. However, we also observed occasional sites where one factor appeared to bind preferentially. The most striking of these was a conserved sequence that bound large amounts of AOD2 but little AOD5. This sequence was found within a 310 bp repeat unit that occurs at several locations in the genome.

蟋蟀神经孢子的替代氧化酶转录因子 AOD2 和 AOD5 控制参与能量生产和代谢的基因的表达。
在克氏黑孢子(Neurospora crassa)中,阻断标准线粒体电子传递链的功能会诱导出替代氧化酶(AOX)。AOX 直接将电子从泛醌传递到分子氧。AOX 是逆向调控的典范,因为它是由核基因编码的,而核基因是根据来自线粒体的信号进行调控的。N. crassa 的转录因子 AOD2 和 AOD5 是 AOX 基因表达所必需的。为了深入了解这些因子的作用机制,并确定它们是否在 N. crassa 其它基因的表达中发挥作用,我们构建了仅表达这两种蛋白标记版本的菌株。细胞分馏实验表明,在 AOX 诱导和非诱导条件下,这两种蛋白都定位于细胞核。此外,染色质免疫沉淀和高通量测序(ChIP-seq)分析表明,在这两种条件下,这两种蛋白都与 AOX 基因的启动子区域结合。ChIP-seq 还显示,转录因子与一些参与能量产生和代谢的基因的上游区域结合。定量 PCR 验证了其中几个基因的表达依赖于 AOD2 和 AOD5。观察到的大多数 ChIP-seq 峰同时富集了 AOD2 和 AOD5。不过,我们也偶尔观察到一个因子似乎优先结合的位点。其中最引人注目的是一个保守序列,它结合了大量的 AOD2,却很少结合 AOD5。该序列出现在基因组中多个位置的 310 bp 重复单元中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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