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2
The fungal acl1 and acl2 genes encode two polypeptides with homology to the N- and C-terminal parts of the animal ATP citrate lyase polypeptide.真菌的acl1和acl2基因编码两种与动物ATP柠檬酸裂解酶多肽的N端和C端部分具有同源性的多肽。
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本文引用的文献

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The control of fruiting body formation in the ascomycete Sordaria macrospora Auersw. by arginine and biotin: a two-factor analysis.在子囊菌 Sordaria macrospora Auersw. 中通过精氨酸和生物素控制子实体形成:两因素分析。
Planta. 1976 Jan;128(2):143-8. doi: 10.1007/BF00390315.
2
Structural and transcription analysis of two homologous genes for the P700 chlorophyll a-apoproteins in Chlamydomonas reinhardii: evidence for in vivo trans-splicing.莱茵衣藻 P700 叶绿素 a 脱辅基蛋白的两个同源基因的结构和转录分析:体内反式剪接的证据。
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[Genetic studies on Sordaria macrospora Auersw., compensation and induction in gene-dependent developmental defects].[大孢粪壳菌(Sordaria macrospora Auersw.)的遗传学研究、基因依赖性发育缺陷中的补偿与诱导]
Z Vererbungsl. 1958;89(5):729-46.
4
Changes in fatty acid composition of Neurospora crassa accompany sexual development and ascospore germination.粗糙脉孢菌脂肪酸组成的变化伴随着有性发育和子囊孢子萌发。
Microbiology (Reading). 1998 Jul;144 ( Pt 7):1713-1720. doi: 10.1099/00221287-144-7-1713.
5
ATP: citrate lyase from Aspergillus nidulans.ATP:来自构巢曲霉的柠檬酸裂解酶。
Biochem Soc Trans. 1997 Nov;25(4):S670. doi: 10.1042/bst025s670.
6
Mating types and sexual development in filamentous ascomycetes.丝状子囊菌的交配型与有性发育
Microbiol Mol Biol Rev. 1997 Dec;61(4):411-28. doi: 10.1128/mmbr.61.4.411-428.1997.
7
Mating-type genes from the homothallic fungus Sordaria macrospora are functionally expressed in a heterothallic ascomycete.来自同宗配合真菌大孢粪壳菌的交配型基因在异宗配合子囊菌中实现了功能表达。
Genetics. 1997 Oct;147(2):567-80. doi: 10.1093/genetics/147.2.567.
8
The reductive tricarboxylic acid cycle of carbon dioxide assimilation: initial studies and purification of ATP-citrate lyase from the green sulfur bacterium Chlorobium tepidum.二氧化碳同化的还原性三羧酸循环:来自嗜热绿硫细菌绿热栖菌的ATP-柠檬酸裂解酶的初步研究及纯化
J Bacteriol. 1997 Aug;179(15):4859-67. doi: 10.1128/jb.179.15.4859-4867.1997.
9
A putative rhamnogalacturonase required for sexual development of Neurospora crassa.一种粗糙脉孢菌有性发育所需的假定鼠李半乳糖醛酸酶。
Genetics. 1997 Jun;146(2):531-40. doi: 10.1093/genetics/146.2.531.
10
rco-3, a gene involved in glucose transport and conidiation in Neurospora crassa.rco-3,一种参与粗糙脉孢菌葡萄糖转运和分生孢子形成的基因。
Genetics. 1997 Jun;146(2):499-508. doi: 10.1093/genetics/146.2.499.

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.

DOI:10.1128/MCB.19.1.450
PMID:9858569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC83903/
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。