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粗糙脉孢菌arg-12基因的克隆及其转录通过跨途径氨基酸控制的调节。

Cloning of the arg-12 gene of Neurospora crassa and regulation of its transcript via cross-pathway amino acid control.

作者信息

Flint H J, Wilkening J

出版信息

Mol Gen Genet. 1986 Apr;203(1):110-6. doi: 10.1007/BF00330391.

DOI:10.1007/BF00330391
PMID:3012277
Abstract

The arg-12 locus of Neurospora crassa encodes ornithine carbamoyl transferase, which is one of many amino acid synthetic enzymes whose activity is regulated through cross-pathway (or general) amino acid control. We report here the use of probes derived from the functionally equivalent arg-B gene of Aspergillus nidulans to identify and clone a 10 kb Neurospora DNA fragment carrying the arg-12 gene. Short Neurospora DNA probes derived from this fragment were used to identify a 1.5 kb polyA+ transcript of the arg-12 region. Arg-12 transcript levels increased approximately 20 fold under conditions of arginine or histidine limitation in strains having normal cross-pathway regulation (cpc-1+) but showed no such response in a cpc-1 mutant strain impaired in this regulation. Time course studies in cpc-1+ strains revealed a rapid response (within 10 m) of arg-12 transcript levels following inhibition of histidine synthesis by 3 amino 1,2,4 triazole, but a delayed response following arginine deprivation of an arginine requiring strain. In contrast to the behaviour of arg-12 mRNA, the level of the Neurospora am gene transcript (specifying NADP dependent glutamate dehydrogenase) was unaffected either by amino acid limitation or by the cpc-1 mutation. A possible role for the cpc-1+ product as a positive regulator of transcription of genes subject to cross-pathway control is discussed.

摘要

粗糙脉孢菌的arg-12基因座编码鸟氨酸氨甲酰基转移酶,它是众多氨基酸合成酶之一,其活性通过交叉途径(或一般)氨基酸控制来调节。我们在此报告,利用来自构巢曲霉功能等效的arg-B基因的探针,鉴定并克隆了一个携带arg-12基因的10 kb脉孢菌DNA片段。从该片段衍生的短脉孢菌DNA探针用于鉴定arg-12区域的一个1.5 kb多聚腺苷酸加尾转录本。在具有正常交叉途径调节(cpc-1+)的菌株中,在精氨酸或组氨酸受限的条件下,Arg-12转录水平增加约20倍,但在这种调节受损的cpc-1突变菌株中未显示出这种反应。在cpc-1+菌株中的时间进程研究表明,用3-氨基-1,2,4-三唑抑制组氨酸合成后,arg-12转录水平迅速反应(在10分钟内),但在精氨酸需求菌株精氨酸剥夺后反应延迟。与arg-12 mRNA的行为相反,脉孢菌am基因转录本(指定NADP依赖性谷氨酸脱氢酶)的水平不受氨基酸限制或cpc-1突变的影响。讨论了cpc-1+产物作为受交叉途径控制基因转录的正调节因子的可能作用。

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Cloning of the arg-12 gene of Neurospora crassa and regulation of its transcript via cross-pathway amino acid control.粗糙脉孢菌arg-12基因的克隆及其转录通过跨途径氨基酸控制的调节。
Mol Gen Genet. 1986 Apr;203(1):110-6. doi: 10.1007/BF00330391.
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The cross-pathway control gene of Neurospora crassa, cpc-1, encodes a protein similar to GCN4 of yeast and the DNA-binding domain of the oncogene v-jun-encoded protein.粗糙脉孢菌的交叉途径控制基因cpc-1编码一种与酵母的GCN4以及癌基因v-jun编码蛋白的DNA结合结构域相似的蛋白质。
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Regulation of amino acid synthetic enzymes in Neurospora crassa in the presence of high concentrations of amino acids.在高浓度氨基酸存在的情况下,粗糙脉孢菌中氨基酸合成酶的调控。
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本文引用的文献

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General control of arginine biosynthetic enzymes in Neurospora crassa.粗糙脉孢菌中精氨酸生物合成酶的总体调控
J Gen Microbiol. 1981 May;124(1):129-40. doi: 10.1099/00221287-124-1-129.
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5' untranslated sequences are required for the translational control of a yeast regulatory gene.酵母调控基因的翻译控制需要5'非翻译序列。
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在粗糙脉孢菌中,编码漆酶的环己酰亚胺诱导型基因的转录激活由交叉途径控制基因cpc-1介导。
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Mechanisms of gene regulation in the general control of amino acid biosynthesis in Saccharomyces cerevisiae.酿酒酵母中氨基酸生物合成一般调控中的基因调控机制。
Microbiol Rev. 1988 Jun;52(2):248-73. doi: 10.1128/mr.52.2.248-273.1988.
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The cross-pathway control gene of Neurospora crassa, cpc-1, encodes a protein similar to GCN4 of yeast and the DNA-binding domain of the oncogene v-jun-encoded protein.粗糙脉孢菌的交叉途径控制基因cpc-1编码一种与酵母的GCN4以及癌基因v-jun编码蛋白的DNA结合结构域相似的蛋白质。
Proc Natl Acad Sci U S A. 1988 Jun;85(11):3728-32. doi: 10.1073/pnas.85.11.3728.
6
Compartmental and regulatory mechanisms in the arginine pathways of Neurospora crassa and Saccharomyces cerevisiae.粗糙脉孢菌和酿酒酵母精氨酸途径中的区室化和调节机制。
Microbiol Rev. 1986 Sep;50(3):280-313. doi: 10.1128/mr.50.3.280-313.1986.
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Regulation of amino acid synthetic enzymes in Neurospora crassa in the presence of high concentrations of amino acids.在高浓度氨基酸存在的情况下,粗糙脉孢菌中氨基酸合成酶的调控。
Mol Gen Genet. 1986 Jun;203(3):533-7. doi: 10.1007/BF00422082.
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Molecular cloning and analysis of the regulation of nit-3, the structural gene for nitrate reductase in Neurospora crassa.粗糙脉孢菌中硝酸还原酶结构基因nit-3调控的分子克隆与分析。
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8243-7. doi: 10.1073/pnas.84.23.8243.
9
Restricted activation of general amino acid control under conditions of glutamine limitation in Neurospora crassa.
Mol Gen Genet. 1990 Sep;223(3):443-8. doi: 10.1007/BF00264452.
10
cpc-2, a new locus involved in general control of amino acid synthetic enzymes in Neurospora crassa.cpc-2,粗糙脉孢菌中参与氨基酸合成酶总体调控的一个新基因座。
Curr Genet. 1990 Oct;18(3):211-5. doi: 10.1007/BF00318383.
Proc Natl Acad Sci U S A. 1984 Oct;81(20):6442-6. doi: 10.1073/pnas.81.20.6442.
4
Cloning and characterization of the ornithine carbamoyltransferase gene from Aspergillus nidulans.构巢曲霉鸟氨酸氨甲酰基转移酶基因的克隆与特性分析
Gene. 1983 Nov;25(1):109-17. doi: 10.1016/0378-1119(83)90173-7.
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Positive regulation in the general amino acid control of Saccharomyces cerevisiae.酿酒酵母一般氨基酸控制中的正调控
Proc Natl Acad Sci U S A. 1983 Sep;80(17):5374-8. doi: 10.1073/pnas.80.17.5374.
6
Identification of AAS genes and their regulatory role in general control of amino acid biosynthesis in yeast.酵母中氨基酸合成相关基因的鉴定及其在氨基酸生物合成总体调控中的作用。
Proc Natl Acad Sci U S A. 1983 May;80(9):2704-8. doi: 10.1073/pnas.80.9.2704.
7
A short nucleotide sequence required for regulation of HIS4 by the general control system of yeast.酵母通用控制系统调控HIS4所必需的一段短核苷酸序列。
Cell. 1983 Jan;32(1):89-98. doi: 10.1016/0092-8674(83)90499-3.
8
Temporal analysis of general control of amino acid biosynthesis in Saccharomyces cerevisiae: role of positive regulatory genes in initiation and maintenance of mRNA derepression.酿酒酵母氨基酸生物合成一般控制的时间分析:正调控基因在mRNA去阻遏起始和维持中的作用。
Mol Cell Biol. 1984 Mar;4(3):520-8. doi: 10.1128/mcb.4.3.520-528.1984.
9
Cloning of the am (glutamate dehydrogenase) gene of Neurospora crassa through the use of a synthetic DNA probe.利用合成DNA探针克隆粗糙脉孢菌的am(谷氨酸脱氢酶)基因。
Gene. 1982 Dec;20(3):387-96. doi: 10.1016/0378-1119(82)90207-4.
10
The primary structure of the alcohol dehydrogenase gene from the fission yeast Schizosaccharomyces pombe.来自裂殖酵母粟酒裂殖酵母的乙醇脱氢酶基因的一级结构。
J Biol Chem. 1983 Jan 10;258(1):143-9.