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首页> 外文期刊>BMC Genomics >Implications of high level pseudogene transcription in Mycobacterium leprae
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Implications of high level pseudogene transcription in Mycobacterium leprae

机译:麻风分枝杆菌中高水平假基因转录的意义

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Background The Mycobacterium leprae genome has less than 50% coding capacity and 1,133 pseudogenes. Preliminary evidence suggests that some pseudogenes are expressed. Therefore, defining pseudogene transcriptional and translational potentials of this genome should increase our understanding of their impact on M. leprae physiology. Results Gene expression analysis identified transcripts from 49% of all M. leprae genes including 57% of all ORFs and 43% of all pseudogenes in the genome. Transcribed pseudogenes were randomly distributed throughout the chromosome. Factors resulting in pseudogene transcription included: 1) co-orientation of transcribed pseudogenes with transcribed ORFs within or exclusive of operon-like structures; 2) the paucity of intrinsic stem-loop transcriptional terminators between transcribed ORFs and downstream pseudogenes; and 3) predicted pseudogene promoters. Mechanisms for translational "silencing" of pseudogene transcripts included the lack of both translational start codons and strong Shine-Dalgarno (SD) sequences. Transcribed pseudogenes also contained multiple "in-frame" stop codons and high Ka/Ks ratios, compared to that of homologs in M. tuberculosis and ORFs in M. leprae. A pseudogene transcript containing an active promoter, strong SD site, a start codon, but containing two in frame stop codons yielded a protein product when expressed in E. coli. Conclusion Approximately half of M. leprae's transcriptome consists of inactive gene products consuming energy and resources without potential benefit to M. leprae. Presently it is unclear what additional detrimental affect(s) this large number of inactive mRNAs has on the functional capability of this organism. Translation of these pseudogenes may play an important role in overall energy consumption and resultant pathophysiological characteristics of M. leprae. However, this study also demonstrated that multiple translational "silencing" mechanisms are present, reducing additional energy and resource expenditure required for protein production from the vast majority of these transcripts.
机译:背景麻风分枝杆菌基因组的编码能力不足50%,假基因为1,133个。初步证据表明表达了一些假基因。因此,定义该基因组的假基因转录和翻译潜能应该增加我们对它们对麻风分枝杆菌生理的影响的理解。结果基因表达分析从基因组中所有麻风分枝杆菌基因的49%中识别出转录本,包括所有ORF中的57%和所有假基因中的43%。转录的假基因随机分布在整个染色体中。导致假基因转录的因素包括:1)转录的假基因与转录的ORF在操纵子样结构内或之外的共取向; 2)转录的ORF和下游假基因之间缺乏内在的茎环转录终止子; 3)预测的假基因启动子。伪基因转录本的翻译“沉默”机制包括缺乏翻译起始密码子和强Shine-Dalgarno(SD)序列。与结核分枝杆菌的同系物和麻疯分枝杆菌的ORF相比,转录的假基因还包含多个“框内”终止密码子和高Ka / Ks比。当在大肠杆菌中表达时,含有活性启动子,强SD位点,起始密码子但含有两个框内终止密码子的假基因转录物产生蛋白质产物。结论麻风分枝杆菌的转录组中约有一半由无活性的基因产物组成,这些产品消耗能量和资源而对麻风分枝杆菌没有潜在的好处。目前尚不清楚这种大量的非活性mRNAs对该生物体的功能能力有哪些额外的有害影响。这些假基因的翻译可能在麻风总能量消耗和由此产生的病理生理特征中起重要作用。但是,这项研究还表明存在多种翻译“沉默”机制,可减少这些转录物中绝大多数产生蛋白质所需的额外能量和资源消耗。

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