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粗糙脉孢菌中一个硝酸盐转运蛋白基因的鉴定与特性分析。

Identification and characterization of a nitrate transporter gene in Neurospora crassa.

作者信息

Gao-Rubinelli Fei, Marzluf George A

机构信息

Department of Biochemistry, Ohio State University, Columbus, Ohio 43210, USA.

出版信息

Biochem Genet. 2004 Feb;42(1-2):21-34. doi: 10.1023/b:bigi.0000012141.51114.23.

DOI:10.1023/b:bigi.0000012141.51114.23
PMID:15068336
Abstract

The Neurospora crassa genome database was searched for sequence similarity to crnA, a nitrate transporter in Aspergillus nidulans. A 3.9-kb fragment (contig 3.416, subsequence 183190-187090) was cloned by PCR. The gene coding for this nitrate transporter was termed nit-10. The nit-10 gene specifies a predicted polypeptide containing 541 amino acids with a molecular mass of 57 kDa. In contrast to crnA, which is clustered together with niaD, encoding nitrate reductase, and niiA, encoding nitrite reductase, nit-10 is not linked to nit-3 (nitrate reductase), nit-6 (nitrite reductase), or to nit-2, nit-4 (both are positive regulators of nit-3), or nmr (negative regulator of nit-3) in Neurospora crassa. A nit-10 rip mutant failed to grow in the medium when nitrate (< 10 mM) was used as the sole nitrogen source, but grew similarly to wild type when nitrate concentration was 10 mM or higher. In addition, it showed strong sensitivity to cesium in the presence of nitrate and resistance to chlorate in the presence of alanine, proline, or hypoxanthine. The expression of nit-10 required nitrate induction and was subject to repression by nitrogen metabolites such as glutamine. Expression of nit-10 also required functional products of nit-2 and nit-4. The half-life of nit-10 mRNA was determined to be approximately 2.5 min.

摘要

在粗糙脉孢菌基因组数据库中搜索与构巢曲霉中的硝酸盐转运蛋白crnA序列相似的序列。通过PCR克隆到一个3.9 kb的片段(重叠群3.416,子序列183190 - 187090)。编码该硝酸盐转运蛋白的基因被命名为nit - 10。nit - 10基因指定了一个预测的包含541个氨基酸、分子量为57 kDa的多肽。与与编码硝酸还原酶的niaD和编码亚硝酸还原酶的niiA聚集在一起的crnA不同,nit - 10在粗糙脉孢菌中不与nit - 3(硝酸还原酶)、nit - 6(亚硝酸还原酶)、或nit - 2、nit - 4(两者都是nit - 3的正调控因子)或nmr(nit - 3的负调控因子)连锁。一个nit - 10 rip突变体在以硝酸盐(< 10 mM)作为唯一氮源的培养基中无法生长,但当硝酸盐浓度为10 mM或更高时,其生长与野生型相似。此外,它在有硝酸盐存在时对铯表现出强烈敏感性,在有丙氨酸、脯氨酸或次黄嘌呤存在时对氯酸盐表现出抗性。nit - 10的表达需要硝酸盐诱导,并受到氮代谢物如谷氨酰胺的抑制。nit - 10的表达还需要nit - 2和nit - 4的功能性产物。nit - 10 mRNA的半衰期测定约为2.5分钟。

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