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矮牵牛硝酸还原酶脱辅基酶编码基因的分析:序列修饰分析的第一步。

Analysis of the petunia nitrate reductase apoenzyme-encoding gene: a first step for sequence modification analysis.

作者信息

Salanoubat M, Bui Dang Ha D

机构信息

Laboratoire de Génétique Végétale, Université Paris-Sud, CNRS, Orsay, France.

出版信息

Gene. 1993 Jun 30;128(2):147-54. doi: 10.1016/0378-1119(93)90557-j.

Abstract

In this paper, we describe the gene (nia) coding for the apoenzyme of the nitrate reductase (NR) of petunia. A full-size genomic clone was isolated from a genomic library, using the tobacco nia2 cDNA as a probe, and sequenced. The open reading frame is interrupted by three introns and encodes a protein of 909 amino acids which reveals between 92% and 68% identity to the NADH NR apoenzyme from other higher plants. Southern analyses indicated that the NR apoenzyme is encoded by a single-copy gene, although another region homologous to part of nia was also identified. The analysis of the steady-state level of nia mRNA showed that the petunia nia is regulated by the nitrogen source and is under the control of the circadian rhythm.

摘要

在本文中,我们描述了矮牵牛硝酸还原酶(NR)脱辅基酶的编码基因(nia)。利用烟草nia2 cDNA作为探针,从基因组文库中分离出一个全长基因组克隆并进行测序。开放阅读框被三个内含子打断,编码一个由909个氨基酸组成的蛋白质,该蛋白质与其他高等植物的NADH NR脱辅基酶具有92%至68%的同一性。Southern分析表明,NR脱辅基酶由单拷贝基因编码,尽管还鉴定出了另一个与nia部分同源的区域。nia mRNA稳态水平的分析表明,矮牵牛nia受氮源调节,并受昼夜节律控制。

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