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Tn1721的完整核苷酸序列:基因组织及一种具有趋化蛋白特征的新型基因产物。

Complete nucleotide sequence of Tn1721: gene organization and a novel gene product with features of a chemotaxis protein.

作者信息

Allmeier H, Cresnar B, Greck M, Schmitt R

机构信息

Lehrstuhl für Genetik, Universität Regensburg, F.R.G.

出版信息

Gene. 1992 Feb 1;111(1):11-20. doi: 10.1016/0378-1119(92)90597-i.

Abstract

The complete 11,139-nucleotide sequence of transposon Tn1721 has been determined. It contains three 38-bp inverted repeats, and (in this order) a new orfI, a resolution site (res), genes encoding resolvase (tnpR), transposase (tnpA), tetracycline-resistance (TcR) repressor (tetR), TcR (tetA) and a truncated transposase gene (tnpA'). The modulator origin of Tn1721 from at least three separate sources is supported by the distinctive codon usages of orfI, tnpR/tnpA and tetR/tetA, and by sequence similarities with Tn501 (tnpR/tnpA) and RP1 (tetR/tetA). The ORFI-encoded 56-kDa polypeptide exhibits features of a methyl-accepting chemotaxis protein (MCP) with a conserved signal domain and a potential transmembrane domain; this polypeptide cross-reacts with anti-MCP antiserum. Like chemotaxis genes, orfI is transcribed from a sigma 28-like promoter. The overexpressed orfI gene product interferes with MCP-dependent chemotaxis suggesting that it completes for soluble transducer protein(s) in the cell. The potential selective advantage of this novel transposon-borne gene is discussed.

摘要

已确定转座子Tn1721完整的11139个核苷酸序列。它包含三个38bp的反向重复序列,且(按此顺序)有一个新的orfI、一个解离位点(res)、编码解离酶(tnpR)、转座酶(tnpA)、四环素抗性(TcR)阻遏物(tetR)、TcR(tetA)的基因以及一个截短的转座酶基因(tnpA')。Tn1721至少有三个独立来源的调节子起源,这一点得到了orfI、tnpR/tnpA和tetR/tetA独特的密码子使用情况以及与Tn501(tnpR/tnpA)和RP1(tetR/tetA)的序列相似性的支持。由ORFI编码的56kDa多肽具有甲基接受趋化蛋白(MCP)的特征,带有一个保守的信号结构域和一个潜在的跨膜结构域;该多肽与抗MCP抗血清发生交叉反应。与趋化基因一样,orfI从一个类σ28启动子转录。过表达的orfI基因产物干扰依赖MCP的趋化作用,这表明它在细胞中与可溶性转导蛋白竞争。本文讨论了这种新型转座子携带基因的潜在选择优势。

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