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阿舒假囊酵母α-因子信息素及其信息素受体基因的特征。

Characterization of α-factor pheromone and pheromone receptor genes of Ashbya gossypii.

机构信息

Carlsberg Laboratory, Yeast Biology, Valby, Copenhagen, Denmark.

出版信息

FEMS Yeast Res. 2011 Aug;11(5):418-29. doi: 10.1111/j.1567-1364.2011.00732.x. Epub 2011 May 6.

Abstract

The genome of Ashbya gossypii contains homologs of most of the genes that are part of the Saccharomyces cerevisiae pheromone-signal transduction cascade. However, we currently lack understanding of a potential sexual cycle for this pre-whole genome duplication hemiascomycete. The sequenced strain bears three identical copies encoding MATa. We show that the syntenic A. gossypii homolog of MFα1 (AFL062w) does not encode a mature α-factor peptide, but identified another gene, AAR163c, which encodes a candidate α-specific mating pheromone and is thus reannotated as AgMFα2. The expression of the AgSTE2α-factor receptor in an Scste2 S. cerevisiae MATa strain resulted in dosage-dependent growth arrest upon exposure to A. gossypiiα-factor, which indicated that the pheromone response was effectively coupled to the S. cerevisiae signal transduction cascade. Comparison of α-pheromones and α-pheromone receptors showed greater conservation between Eremothecium cymbalariae and S. cerevisiae than between A. gossypii and E. cymbalariae. We constructed A. gossypii strains deleted for the STE2 and STE3 pheromone receptors. These strains showed no phenotypic abnormalities and an ste2, ste3 double mutant is still able to sporulate. The deletion of STE12 as the downstream target of pheromone signalling, however, led to a hypersporulation phenotype.

摘要

阿什比棉子囊酵母的基因组包含了大多数与酿酒酵母信息素信号转导级联相关基因的同源物。然而,我们目前还缺乏对这个经历过全基因组倍增的准子囊菌的潜在有性周期的理解。测序菌株有三个相同的 MATa 编码拷贝。我们发现,MFα1(AFL062w)的阿什比棉子囊酵母直系同源物并不编码成熟的α-因子肽,但鉴定出另一个基因 AAR163c,它编码一个候选的α-特异性交配信息素,因此被重新注释为 AgMFα2。在 Scste2 酿酒酵母 MATa 菌株中表达 AgSTE2α-因子受体,在接触到阿什比棉子囊酵母α-因子后会导致剂量依赖性的生长停滞,这表明信息素反应有效地与酿酒酵母信号转导级联相偶联。α-信息素和α-信息素受体的比较表明,埃里默氏菌属和酿酒酵母之间的保守性大于阿什比棉子囊酵母和埃里默氏菌属之间的保守性。我们构建了缺失 STE2 和 STE3 信息素受体的阿什比棉子囊酵母菌株。这些菌株没有表现出任何表型异常,并且 ste2、ste3 双突变体仍然能够进行孢子形成。然而,删除作为信息素信号下游靶标的 STE12 导致了超孢子形成表型。

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