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Overlapping Antisense Transcription in the Human Genome

机译:人类基因组中的反义转录重叠

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Accumulating evidence indicates an important role for non-coding RNA molecules ineukaryotic cell regulation. A small number of coding and non-coding overlapping antisensetranscripts (OATs) in eukaryotes have been reported, some of which regulate expression ofthe corresponding sense transcript. The prevalence of this phenomenon is unknown, butthere may be an enrichment of such transcripts at imprinted gene loci. Taking a bioinformaticsapproach, we systematically searched a human mRNA database (RefSeq) for complementaryregions that might facilitate pairing with other transcripts. We report 56 pairsof overlapping transcripts, in which each member of the pair is transcribed from the samelocus. This allows us to make an estimate of 1000 for the minimum number of suchtranscript pairs in the entire human genome. This is a surprisingly large number ofoverlapping gene pairs and, clearly, some of the overlaps may not be functionallysignificant. Nonetheless, this may indicate an important general role for overlappingantisense control in gene regulation. EST databases were also investigated in order toaddress the prevalence of cases of imprinted genes with associated non-coding overlapping,antisense transcripts. However, EST databases were found to be completely inappropriatefor this purpose.
机译:越来越多的证据表明,非编码RNA分子对真核细胞的调节具有重要作用。已经报道了真核生物中少量的编码和非编码重叠反义转录物(OAT),其中一些调节相应的有义转录物的表达。这种现象的发生率尚不清楚,但可能会在印​​迹基因位点上丰富此类转录本。采取生物信息学方法,我们系统地搜索了人类mRNA数据库(RefSeq)中可能有助于与其他转录本配对的互补区域。我们报告了56对重叠的笔录,其中每对成员都从同一基因座转录。这样,我们就可以估算出整个人类基因组中此类转录本对的最小数量为1000。这是令人惊讶的大量重叠基因对,而且显然,某些重叠可能在功能上不重要。然而,这可能表明在基因调控中重叠反义控制的重要一般作用。还研究了EST数据库,以解决带有相关非编码重叠,反义转录物的印迹基因病例的普遍性。但是,发现EST数据库完全不适合该目的。

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