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大孢粪壳菌有性发育过程中的细胞分化需要ATP柠檬酸裂解酶的活性。

Cell differentiation during sexual development of the fungus Sordaria macrospora requires ATP citrate lyase activity.

作者信息

Nowrousian M, Masloff S, Pöggeler S, Kück U

机构信息

Lehrstuhl für Allgemeine Botanik, Ruhr-Universität Bochum, D-44780 Bochum, Germany.

出版信息

Mol Cell Biol. 1999 Jan;19(1):450-60. doi: 10.1128/MCB.19.1.450.

Abstract

During sexual development, mycelial cells from most filamentous fungi differentiate into typical fruiting bodies. Here, we describe the isolation and characterization of the Sordaria macrospora developmental mutant per5, which exhibits a sterile phenotype with defects in fruiting body maturation. Cytological investigations revealed that the mutant strain forms only ascus precursors without any mature spores. Using an indexed cosmid library, we were able to complement the mutant to fertility by DNA-mediated transformation. A single cosmid clone, carrying a 3.5-kb region able to complement the mutant phenotype, has been identified. Sequencing of the 3.5-kb region revealed an open reading frame of 2.1 kb interrupted by a 66-bp intron. The predicted polypeptide (674 amino acids) shows significant homology to eukaryotic ATP citrate lyases (ACLs), with 62 to 65% amino acid identity, and the gene was named acl1. The molecular mass of the S. macrospora ACL1 polypeptide is 73 kDa, as was verified by Western blot analysis with a hemagglutinin (HA) epitope-tagged ACL1 polypeptide. Immunological in situ detection of the HA-tagged polypeptide demonstrated that ACL is located within the cytosol. Sequencing of the mutant acl1 gene revealed a 1-nucleotide transition within the coding region, resulting in an amino acid substitution within the predicted polypeptide. Further evidence that ACL1 is essential for fruiting body maturation comes from experiments in which truncated and mutated versions of the acl1 gene were used for transformation. None of these copies was able to reconstitute the fertile phenotype in transformed per5 recipient strains. ACLs are usually involved in the formation of cytosolic acetyl coenzyme A (acetyl-CoA), which is used for the biosynthesis of fatty acids and sterols. Protein extracts from the mutant strain showed a drastic reduction in enzymatic activity compared to values obtained from the wild-type strain. Investigation of the time course of ACL expression suggests that ACL is specifically induced at the beginning of the sexual cycle and produces acetyl-CoA, which most probably is a prerequisite for fruiting body formation during later stages of sexual development. We discuss the contribution of ACL activity to the life cycle of S. macrospora.

摘要

在有性发育过程中,大多数丝状真菌的菌丝体细胞分化为典型的子实体。在此,我们描述了大孢粪壳菌发育突变体per5的分离和特征,该突变体表现出不育表型,子实体成熟存在缺陷。细胞学研究表明,突变菌株仅形成子囊前体,没有任何成熟孢子。利用一个索引黏粒文库,我们通过DNA介导的转化使突变体恢复了育性。已鉴定出一个携带能够互补突变体表型的3.5 kb区域的单个黏粒克隆。对该3.5 kb区域进行测序,发现一个2.1 kb的开放阅读框被一个66 bp的内含子打断。预测的多肽(674个氨基酸)与真核ATP柠檬酸裂解酶(ACL)具有显著同源性,氨基酸同一性为62%至65%,该基因被命名为acl1。通过对带有血凝素(HA)表位标签的ACL1多肽进行蛋白质印迹分析,证实大孢粪壳菌ACL1多肽的分子量为73 kDa。对带有HA标签的多肽进行免疫原位检测表明,ACL位于细胞质中。对突变的acl1基因进行测序,发现在编码区内有一个单核苷酸转换,导致预测多肽内的一个氨基酸替换。ACL1对子实体成熟至关重要的进一步证据来自于使用acl1基因的截短和突变版本进行转化的实验。这些拷贝均无法在转化的per5受体菌株中恢复可育表型。ACL通常参与细胞质乙酰辅酶A(乙酰-CoA)的形成,乙酰-CoA用于脂肪酸和甾醇的生物合成。与野生型菌株相比,突变菌株的蛋白质提取物显示酶活性急剧降低。对ACL表达时间进程的研究表明,ACL在有性周期开始时被特异性诱导,并产生乙酰-CoA,这很可能是有性发育后期子实体形成的先决条件。我们讨论了ACL活性对大孢粪壳菌生命周期的贡献。

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