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鸡毒支原体S6株中pMGA多基因家族四个成员的表达研究

Expression studies on four members of the pMGA multigene family in Mycoplasma gallisepticum S6.

作者信息

Glew M D, Markham P F, Browning G F, Walker I D

机构信息

Department of Veterinary Science, University of Melbourne, Parkville, Australia.

出版信息

Microbiology (Reading). 1995 Nov;141 ( Pt 11):3005-14. doi: 10.1099/13500872-141-11-3005.

DOI:10.1099/13500872-141-11-3005
PMID:8535528
Abstract

A large family of related genes known as pMGA exists in the avian pathogen Mycoplasma gallisepticum but only a single member of this family was previously found to be expressed in one strain of this bacterium. In this work two unrelated strains of M. gallisepticum were also shown by amino-terminal sequencing to express a unique pMGA polypeptide in both cases. To investigate pMGA gene selection in M. gallisepticum, mRNA expression was analysed in M. gallisepticum strain 56 using reverse transcription-PCR (RT-PCR) and Northern blot techniques with probes for several members of the pMGA multigene family. It was shown that the pMGA message is 2.2 kb in size and is monocistronic. RT-PCR detected four different pMGA mRNA molecules but their relative yields were significantly affected by magnesium concentration. By quantitative Northern analysis, the relative abundances of the four pMGA mRNAs in M. gallisepticum S6 total RNA was determined: the pMGA1.1 mRNA predominated [1.88 ng (micrograms total RNA)-1] but at least three other pMGA genes were found to be transcribed but at much lower levels (20 to 40-fold lower). The pMGA1.1 mRNA is expressed at a level five times higher than the tuf gene, known to be one of the most abundantly expressed proteins in the prokaryotic cell. The start point of transcription for pMGA1.1 was determined and probable promoter assigned. From these data it appears likely that transcriptional control plays a major role in the selection of pMGA gene expression in the M. gallisepticum cell.

摘要

在禽病原体鸡毒支原体中存在一个名为pMGA的相关基因大家族,但此前发现该家族中只有一个成员在这种细菌的一个菌株中表达。在这项研究中,通过氨基末端测序还表明,两种不相关的鸡毒支原体菌株在这两种情况下均表达一种独特的pMGA多肽。为了研究鸡毒支原体中pMGA基因的选择,使用逆转录聚合酶链反应(RT-PCR)和Northern印迹技术,用pMGA多基因家族的几个成员的探针,分析了鸡毒支原体56株中的mRNA表达。结果表明,pMGA信息大小为2.2 kb,是单顺反子的。RT-PCR检测到四种不同的pMGA mRNA分子,但它们的相对产量受到镁浓度的显著影响。通过定量Northern分析,确定了鸡毒支原体S6总RNA中四种pMGA mRNA的相对丰度:pMGA1.1 mRNA占主导地位[1.88 ng(每微克总RNA)-1],但至少发现其他三个pMGA基因也被转录,但水平要低得多(低20至40倍)。pMGA1.1 mRNA的表达水平比tuf基因高五倍,tuf基因是已知在原核细胞中表达最丰富的蛋白质之一。确定了pMGA1.1的转录起始点并确定了可能的启动子。从这些数据来看,转录控制似乎在鸡毒支原体细胞中pMGA基因表达的选择中起主要作用。

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