首页> 美国卫生研究院文献>Journal of Bacteriology >Analysis of 0.5-kilobase-pair repeats in the Mycoplasma hominis lmp gene system and identification of gene products.
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Analysis of 0.5-kilobase-pair repeats in the Mycoplasma hominis lmp gene system and identification of gene products.

机译:人型支原体lmp基因系统中0.5碱基对重复序列的分析和基因产物的鉴定。

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摘要

Mycoplasma hominis, an opportunistic pathogenic bacterium of humans, has a small genome of 700 kb. Despite this, multiple copies of gene sequences with similarities to the structural gene (lmp1) of a 135-kDa surface-located membrane protein (Lmp1) have been identified on the genome of M. hominis PG21 (lmp2, lmp3, and lmp4). The distance between the lmp1-lmp2 region and the lmp3-lmp4 region was more than 110 kb. lmp3-lmp4 of M. hominis PG21 was sequenced and found to contain two putative genes. The gene region of 6.5 kb contained a 5' unique region and a 3' unique region separated by 9 0.5-kb repeats with 51 to 90% similarity to 10 similar repeats found in the lmp1-lmp2 region. The 0.5-kb DNA repeats thus comprised about 1% of the entire genome. In both regions, a base change in one of the repeats gave rise to a stop codon, and thereby lmp2 and lmp4 occurred. By PCR amplification of reverse-transcriptase-generated cDNA it was shown that all four genes were transcribed. By use of Lmp-specific antibodies we showed that both lmp1 and lmp3 were translated into proteins (Lmp1 and Lmp3). Each of the four lmp genes represented by their unique cloned segments was used as a probe to analyze the presence, distribution, and organization of the genes within the genome in 13 M. hominis isolates. The repetitive element was detected at one or two locations on the chromosome for all isolates. The lmp3-specific element was present in all isolates, and lmp1- and lmp2-specific elements were present in all but one isolate. The lmp4-specific element was present in about half the isolates tested. For five M. hominis isolates the chromosomal location of the lmp genes was mapped.
机译:人支原体支原体是人的一种机会致病细菌,它的基因组很小,只有700 kb。尽管如此,已在人型支原体PG21(lmp2,lmp3和lmp4)的基因组上鉴定了与135 kDa表面定位膜蛋白(Lmp1)的结构基因(lmp1)具有相似性的基因序列的多个副本。 lmp1-lmp2区域和lmp3-lmp4区域之间的距离大于110 kb。对人型支原体PG21的lmp3-lmp4进行了测序,发现含有两个推定基因。 6.5 kb的基因区域包含一个5'独特区域和一个3'独特区域,这些区域被9个0.5-kb重复序列分隔,与lmp1-lmp2区域中的10个相似重复序列具有51%至90%的相似性。因此,0.5kb的DNA重复占整个基因组的约1%。在这两个区域中,重复序列之一的碱基改变产生了终止密码子,从而产生了lmp2和lmp4。通过逆转录酶产生的cDNA的PCR扩增,表明所有四个基因都被转录。通过使用Lmp特异性抗体,我们表明lmp1和lmp3均被翻译成蛋白质(Lmp1和Lmp3)。以其独特的克隆片段代表的四个lmp基因中的每一个均用作探针,用于分析13 M. hominis分离物中基因组内基因的存在,分布和组织。对于所有分离株,在染色体上的一或两个位置检测到重复元件。 lmp3特异性元件存在于所有分离株中,lmp1和lmp2特异性元件存在于一个分离株中。 lmp4特异元件存在于约一半测试的分离物中。对于五个人型分枝杆菌,对lmp基因的染色体位置进行了定位。

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