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粗糙脉孢菌中嘌呤碱转运的遗传与代谢调控

Genetic and metabolic regulation of purine base transport in Neurospora crassa.

作者信息

Tsao T F, Marzluf G A

出版信息

Mol Gen Genet. 1976 Dec 22;149(3):347-55. doi: 10.1007/BF00268537.

DOI:10.1007/BF00268537
PMID:139563
Abstract

Neurospora crassa can utilize various purine bases such as xanthine or uric acid and their catabolic products as a nitrogen source. The early purine catabolic enzymes in this organism are regulated by induction and by ammonium repression. Studies were undertaken to investigate purine base transport and its regulation in Neurospora. The results of competition experiments with uric acid and xanthine transport strongly suggest that uric acid and xanthine share a common transport system. It was also shown that the common transport system for uric acid and xanthine is distinct from a second transport system shared by hypoxanthine, adenine and guanine, and apparently also distinct from the transport system(s) for adenosine, cytosine and uracil. Regulation of the uric acid-xanthine transport system and the hypoxanthine-adenine-guanine transport system was studied. The results reveal that the uric acid-xanthine transport system is regulated by ammonium repression, but does not require uric acid induction. Neither ammonium repression nor uric acid induction controls the hypoxanthine-adenine-guanine transport system. A gene, designated amr, which is believed to be a positive regulatory gene for nitrogen metabolism of Neurospora crassa, was found to dramatically affect both the uric acid-xanthine transport system and the hypoxanthine-adenine-guanine transport system. A model for the action of the amr locus as a positive regulatory gene and for the interaction between the amr gene product and its recognition sites will be discussed.

摘要

粗糙脉孢菌能够利用各种嘌呤碱,如黄嘌呤或尿酸及其分解代谢产物作为氮源。该生物体中早期的嘌呤分解代谢酶受诱导和铵抑制的调节。开展了研究以调查粗糙脉孢菌中嘌呤碱的转运及其调节。尿酸和黄嘌呤转运的竞争实验结果强烈表明尿酸和黄嘌呤共享一个共同的转运系统。还表明尿酸和黄嘌呤的共同转运系统与次黄嘌呤、腺嘌呤和鸟嘌呤共享的第二个转运系统不同,并且显然也与腺苷、胞嘧啶和尿嘧啶的转运系统不同。研究了尿酸 - 黄嘌呤转运系统和次黄嘌呤 - 腺嘌呤 - 鸟嘌呤转运系统的调节。结果表明尿酸 - 黄嘌呤转运系统受铵抑制调节,但不需要尿酸诱导。铵抑制和尿酸诱导均不控制次黄嘌呤 - 腺嘌呤 - 鸟嘌呤转运系统。发现一个名为amr的基因,它被认为是粗糙脉孢菌氮代谢的正调控基因,对尿酸 - 黄嘌呤转运系统和次黄嘌呤 - 腺嘌呤 - 鸟嘌呤转运系统都有显著影响。将讨论amr基因座作为正调控基因的作用模型以及amr基因产物与其识别位点之间的相互作用。

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Genetic and metabolic regulation of purine base transport in Neurospora crassa.粗糙脉孢菌中嘌呤碱转运的遗传与代谢调控
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Distinction between Hypoxanthine and Xanthine Transport in Chlamydomonas reinhardtii.蓝藻门衣藻中次黄嘌呤和黄嘌呤的转运区别。
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Nitrogen metabolite repression of fluoropyrimidine resistance and pyrimidine uptake in Neurospora crassa.粗糙脉孢菌中氟嘧啶抗性和嘧啶摄取的氮代谢物阻遏

本文引用的文献

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Adenine uptake and pool formation in the fission yeast Schizosaccharomyces pombe.裂殖酵母粟酒裂殖酵母中的腺嘌呤摄取与库形成。
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Implications of some genetic control mechanisms in Neurospora.粗糙脉孢菌中一些遗传控制机制的影响
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Nitrogen regulation of uricase synthesis in Neurospora crassa.粗糙脉孢菌中尿酸酶合成的氮调节
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Nitrogen regulation of amino acid catabolism in Neurospora crassa.粗糙脉孢菌中氨基酸分解代谢的氮调节
Biochem Genet. 1978 Apr;16(3-4):343-54. doi: 10.1007/BF00484090.
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Purine base transport in nit-2 mutants of Neurospora crassa.粗糙脉孢菌nit-2突变体中的嘌呤碱基转运
J Bacteriol. 1978 Jan;133(1):401-2. doi: 10.1128/jb.133.1.401-402.1978.
Biochim Biophys Acta. 1970;209(2):269-77. doi: 10.1016/0005-2787(70)90725-2.
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Nucleoside uptake during the germination of Neurospora crassa conidia.粗糙脉孢菌分生孢子萌发过程中的核苷摄取。
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Nitrogen metabolite repression in Aspergillus nidulans.构巢曲霉中的氮代谢物阻遏
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Evidence for a common transport system for cytosine, adenine and hypoxanthine in Saccharomyces cerevisiae and Candida albicans.酿酒酵母和白色念珠菌中胞嘧啶、腺嘌呤和次黄嘌呤共同转运系统的证据。
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Uptake and accumulation of purine bases by stationary yeast cells pretreated with glucose.用葡萄糖预处理的静止酵母细胞对嘌呤碱的摄取和积累。
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The uptake and incorporation of purines by wild-type Saccharomyces cerevisiae and a mutant resistant to 4-aminopyrazolo (3,4-d) pyrimidine.野生型酿酒酵母和对4-氨基吡唑并(3,4-d)嘧啶耐药的突变体对嘌呤的摄取和掺入。
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Relationship between (8-14C)adenosine transport and growth inhibition in Neurospora crassa strain ad-8.粗糙脉孢菌ad-8菌株中(8-14C)腺苷转运与生长抑制之间的关系
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Genetic and metabolic control of the purine catabolic enzymes of Neurospora crasse.粗糙脉孢菌嘌呤分解代谢酶的遗传与代谢控制
Mol Gen Genet. 1975 Aug 5;139(1):39-55. doi: 10.1007/BF00267994.