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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Three alpha-subunits of heterotrimeric G proteins and an adenylyl cyclase have distinct roles in fruiting body development in the homothallic fungus Sordaria macrospora.
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Three alpha-subunits of heterotrimeric G proteins and an adenylyl cyclase have distinct roles in fruiting body development in the homothallic fungus Sordaria macrospora.

机译:异三聚体G蛋白的三个α亚基和一个腺苷酸环化酶在同型真菌Sordaria macrospora的子实体发育中具有不同的作用。

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摘要

Sordaria macrospora, a self-fertile filamentous ascomycete, carries genes encoding three different alpha-subunits of heterotrimeric G proteins (gsa, G protein Sordaria alpha subunit). We generated knockout strains for all three gsa genes (Deltagsa1, Deltagsa2, and Deltagsa3) as well as all combinations of double mutants. Phenotypic analysis of single and double mutants showed that the genes for Galpha-subunits have distinct roles in the sexual life cycle. While single mutants show some reduction of fertility, double mutants Deltagsa1Deltagsa2 and Deltagsa1Deltagsa3 are completely sterile. To test whether the pheromone receptors PRE1 and PRE2 mediate signaling via distinct Galpha-subunits, two recently generated Deltapre strains were crossed with all Deltagsa strains. Analyses of the corresponding double mutants revealed that compared to GSA2, GSA1 is a more predominant regulator of a signal transduction cascade downstream of the pheromone receptors and that GSA3 is involved in another signaling pathway that also contributes to fruiting body development and fertility. We further isolated the gene encoding adenylyl cyclase (AC) (sac1) for construction of a knockout strain. Analyses of the three DeltagsaDeltasac1 double mutants and one Deltagsa2Deltagsa3Deltasac1 triple mutant indicate that SAC1 acts downstream of GSA3, parallel to a GSA1-GSA2-mediated signaling pathway. In addition, the function of STE12 and PRO41, two presumptive signaling components, was investigated in diverse double mutants lacking those developmental genes in combination with the gsa genes. This analysis was further completed by expression studies of the ste12 and pro41 transcripts in wild-type and mutant strains. From the sum of all our data, we propose a model for how different Galpha-subunits interact with pheromone receptors, adenylyl cyclase, and STE12 and thus cooperatively regulate sexual development in S. macrospora.
机译:Sordaria macrospora,一种自育的丝状子囊菌,携带编码异源三聚体G蛋白(gsa,G蛋白Sordaria alpha亚基)的三个不同α亚基的基因。我们为所有三个gsa基因(Deltagsa1,Deltagsa2和Deltagsa3)以及双重突变体的所有组合产生了敲除菌株。对单突变体和双突变体的表型分析表明,Galpha亚基的基因在性生活周期中具有独特的作用。尽管单个突变体显示出某些降低的繁殖力,但双突变体Deltagsa1Deltagsa2和Deltagsa1Deltagsa3完全不育。为了测试信息素受体PRE1和PRE2是否通过不同的Galpha亚基介导信号传导,将两个最近生成的Deltapre菌株与所有Deltagsa菌株杂交。对相应双突变体的分析表明,与GSA2相比,GSA1是信息素受体下游的信号转导级联的更主要调节因子,并且GSA3参与了另一个有助于子实体发育和生育的信号通路。我们进一步分离了编码腺苷酸环化酶(AC)(sac1)的基因,用于构建敲除菌株。对三个DeltagsaDeltasac1双突变体和一个Deltagsa2Deltagsa3Deltasac1三突变体的分析表明,SAC1在GSA3的下游起作用,与GSA1-GSA2介导的信号通路平行。此外,在缺乏那些与gsa基因结合的发育基因的多种双突变体中,对两个推测性信号传导元件STE12和PRO41的功能进行了研究。通过在野生型和突变菌株中对ste12和pro41转录本的表达研究进一步完成了该分析。从所有数据的总和中,我们提出了一个模型,用于研究不同的Galpha亚基如何与信息素受体,腺苷酸环化酶和STE12相互作用,从而共同调节大孢链霉菌的性发育。

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