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通过新型两步基因步移法对由两个微管蛋白和一个类驱动蛋白基因组成的细菌操纵子进行表征。

Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method.

作者信息

Pilhofer Martin, Bauer Andreas Peter, Schrallhammer Martina, Richter Lothar, Ludwig Wolfgang, Schleifer Karl-Heinz, Petroni Giulio

机构信息

Lehrstuhl für Mikrobiologie, Technical University Munich, Am Hochanger 4, D-85354 Freising, Germany.

出版信息

Nucleic Acids Res. 2007;35(20):e135. doi: 10.1093/nar/gkm836. Epub 2007 Oct 16.

Abstract

Tubulins are still considered as typical proteins of Eukaryotes. However, more recently they have been found in the unusual bacteria Prosthecobacter (btubAB). In this study, the genomic organization of the btub-genes and their genomic environment were characterized by using the newly developed Two-Step Gene Walking method. In all investigated Prosthecobacters, btubAB are organized in a typical bacterial operon. Strikingly, all btub-operons comprise a third gene with similarities to kinesin light chain sequences. The genomic environments of the characterized btub-operons are always different. This supports the hypothesis that this group of genes represents an independent functional unit, which was acquired by Prosthecobacter via horizontal gene transfer. The newly developed Two-Step Gene Walking method is based on randomly primed polymerase chain reaction (PCR). It presents a simple workflow, which comprises only two major steps--a Walking-PCR with a single specific outward pointing primer (step 1) and the direct sequencing of its product using a nested specific primer (step 2). Two-Step Gene Walking proved to be highly efficient and was successfully used to characterize over 20 kb of sequence not only in pure culture but even in complex non-pure culture samples.

摘要

微管蛋白仍被视为真核生物的典型蛋白质。然而,最近在 Prosthecobacter 这种特殊细菌(btubAB)中发现了它们。在本研究中,通过使用新开发的两步基因步移法对 btub 基因的基因组组织及其基因组环境进行了表征。在所有研究的 Prosthecobacter 中,btubAB 以典型的细菌操纵子形式组织。引人注目的是,所有 btub 操纵子都包含一个与驱动蛋白轻链序列相似的第三个基因。已表征的 btub 操纵子的基因组环境总是不同的。这支持了这样一种假设,即这组基因代表一个独立的功能单元,是 Prosthecobacter 通过水平基因转移获得的。新开发的两步基因步移法基于随机引物聚合酶链反应(PCR)。它呈现出一个简单的工作流程,仅包括两个主要步骤——使用单个特异性外向引物进行步移 PCR(步骤 1)以及使用巢式特异性引物对其产物进行直接测序(步骤 2)。两步基因步移法被证明是高效的,并且不仅成功用于纯培养物中超过 20 kb 序列的表征,甚至还用于复杂的非纯培养物样品中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34cd/2175320/5716227bf08e/gkm836f1.jpg

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