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Redox Regulation of an AP-1-Like Transcription Factor, YapA, in the Fungal Symbiont Epichlo? festucae

机译:真菌共生上肢动物中AP-1-转录因子YapA的氧化还原调节?羊茅

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One of the central regulators of oxidative stress in Saccharomyces cerevisiae is Yap1, a bZIP transcription factor of the AP-1 family. In unstressed cells, Yap1 is reduced and cytoplasmic, but in response to oxidative stress, it becomes oxidized and accumulates in the nucleus. To date, there have been no reports on the role of AP-1-like transcription factors in symbiotic fungi. An ortholog of Yap1, named YapA, was identified in the genome of the grass symbiont Epichlo? festucae and shown to complement an S. cerevisiae Δyap1 mutant. Hyphae of the E. festucae ΔyapA strain were sensitive to menadione and diamide but resistant to H2O2, KO2, and tert-butyl hydroperoxide (t-BOOH). In contrast, conidia of the ΔyapA strain were very sensitive to H2O2 and failed to germinate. Using a PcatA-eGFP degron-tagged reporter, YapA was shown to be required for expression of a spore-specific catalase gene, catA. Although YapA-EGFP localized to the nucleus in response to host reactive oxygen species during seedling infection, there was no difference in whole-plant and cellular phenotypes of plants infected with the ΔyapA strain compared to the wild-type strain. Homologs of the S. cerevisiae and Schizosaccharomyces pombe redox-sensing proteins (Gpx3 and Tpx1, respectively) did not act as redox sensors for YapA in E. festucae. In response to oxidative stress, YapA-EGFP localized to the nuclei of E. festucae ΔgpxC, ΔtpxA, and ΔgpxC ΔtpxA cells to the same degree as that in wild-type cells. These results show that E. festucae has a robust system for countering oxidative stress in culture and in planta but that Gpx3- or Tpx1-like thiol peroxidases are dispensable for activation of YapA.
机译:酿酒酵母(Saccharomyces cerevisiae)中氧化应激的中央调节剂之一是Yap1,它是AP-1家族的bZIP转录因子。在未受压力的细胞中,Yap1还原并呈细胞质,但响应氧化应激,它被氧化并积聚在细胞核中。迄今为止,还没有关于AP-1样转录因子在共生真菌中的作用的报道。在草共生体Epichlo?的基因组中鉴定到Yap1的直系同源物,名为YapA。并显示出与酿酒酵母Δ yap1 突变体互补。羊茅大肠菌Δ yapA 的菌丝对甲萘醌和二酰胺敏感,但对H 2 O 2 ,KO 2 < / sub>和丁基氢过氧化物( t -BOOH)。相反,Δ yapA 菌株的分生孢子对H 2 O 2 非常敏感,无法发芽。使用P catA-eGFP degron标记的报告基因,YapA被证明是表达孢子特异性过氧化氢酶基因 catA 所必需的。尽管YapA-EGFP在幼苗感染过程中响应宿主活性氧而定位在细胞核上,但与野生型相比,感染Δ yapA 株的植物的全植物和细胞表型没有差异。类型应变。酿酒酵母和粟酒裂殖酵母氧化还原感测蛋白(分别为Gpx3和Tpx1)的同系物不作为festucae中YapA的氧化还原传感器。响应氧化应激,YapA-EGFP定位在鸡爪草的核中Δ gpxC ,Δ tpxA 和Δ gpxC Δ tpxA 细胞的程度与野生型细胞相同。这些结果表明,马蹄莲具有抵抗培养物中和植物中的氧化应激的强大系统,但是对于激活YapA而言,Gpx3-或Tpx1样的巯基过氧化物酶是必需的。

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