首页> 美国卫生研究院文献>Eukaryotic Cell >Ste12 Transcription Factor Homologue CpST12 Is Down-Regulated by Hypovirus Infection and Required for Virulence and Female Fertility of the Chestnut Blight Fungus Cryphonectria parasitica
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Ste12 Transcription Factor Homologue CpST12 Is Down-Regulated by Hypovirus Infection and Required for Virulence and Female Fertility of the Chestnut Blight Fungus Cryphonectria parasitica

机译:Ste12转录因子同源物CpST12被低病毒感染下调并且是栗枯病真菌Cryphonectria parasititica的毒力和女性生殖力所必需的

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摘要

A putative homologue of the Saccharomyces cerevisiae Ste12 transcription factor was identified in a series of expressed sequence tag-based microarray analyses as being down-regulated in strains of the chestnut blight fungus, Cryphonectria parasitica, infected by virulence-attenuating hypoviruses. Cloning of the corresponding gene, cpst12, confirmed a high level of similarity to Ste12 homologues of other filamentous fungi. Disruption of cpst12 resulted in no alterations in in vitro growth characteristics or colony morphology and an increase in the production of asexual spores, indicating that CpST12 is dispensable for vegetative growth and conidiation on artificial medium. However, the disruption mutants showed a very substantial reduction in virulence on chestnut tissue and a complete loss of female fertility, two symptoms normally conferred by hypovirus infection. Both virulence and female fertility were restored by complementation with the wild-type cpst12 gene. Analysis of transcriptional changes caused by cpst12 gene disruption with a custom C. parastica cDNA microaray chip identified 152 responsive genes. A significant number of these putative CpST12-regulated genes were also responsive to hypovirus infection. Thus, cpst12 encodes a cellular transcription factor, CpST12, that is down-regulated by hypovirus infection and required for female fertility, virulence and regulated expression of a subset of hypovirus responsive host genes.
机译:在一系列基于表达序列标签的微阵列分析中,啤酒酵母Ste12转录因子的推定同源物在被致病性减毒次病毒感染的板栗枯萎真菌寄生小隐孢子虫菌株中被下调。相应基因cpst12的克隆证实与其他丝状真菌的Ste12同源物高度相似。 cpst12的破坏不会导致体外生长特征或菌落形态的改变,也不会增加无性孢子的产生,这表明CpST12对于人工培养基上的营养生长和分生是必不可少的。然而,破坏突变体显示出栗子组织上的毒力大大降低,女性生育力完全丧失,这通常是由低病毒感染引起的两种症状。通过与野生型cpst12基因互补可恢复毒力和雌性育性。使用定制的寄生虫毕赤酵母cDNA microaray芯片分析cpst12基因破坏引起的转录变化,鉴定出152个响应基因。这些推定的受CpST12调控的基因中,有大量也对低病毒感染有反应。因此,cpst12编码一种细胞转录因子CpST12,该因子被伪病毒感染下调,并且是女性生育力,毒力和伪病毒应答宿主基因子集表达调控所必需的。

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