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Noncoding RNAs in Health and Disease

机译:非沉积的RNA在健康和疾病中

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摘要

Genome and RNA sequencing have reliably demonstrated that up to 90% of the human genome may be transcribed. According to actual estimates, the proteome genome (i.e., all genomic sequences involved in mRNA synthesis) occupies only up to 4% of the humangenome [1]. The remaining part, which may be provisionally named as noncoding RNA genome (ncRNA genome), comprises genes encoding a plethora of structurally and functionally different RNAs other than mRNAs; since most of these apparently do not code forproteins, they have been labelled noncoding RNAs (ncRNAs) [2]. These data have determined a radical paradigm shift in biomolecular medicine and modified our vision of genome structure and functions. They also changed objectives and perspectives of genomic research. As reminded above, the ncRNA genome very likely occupies a very large molecular space; accordingly, it seems logical to hypothesize that the molecular explanation of important biopathological phenomena (i.e., normal development and differentiation together with their pathological alterations) is to be found in these regions.
机译:基因组和RNA测序可靠地证明,可以转录高达90%的人类基因组。根据实际估计,蛋白质组基因组(即MRNA合成中的所有基因组序列)仅占Humangenome的4%[1]。剩余部分可以被临时命名为非编码RNA基因组(NCRNA基因组),包括编码除MRNA之外的结构和功能不同RNA的过多的基因;由于大多数显然不是代码前蛋白质,因此它们已被标记为非编码RNA(NCRNA)[2]。这些数据已经确定了生物分子药物的激进范式转变,并修改了我们对基因组结构和功能的视野。他们还改变了基因组研究的目标和视角。如上所述,NCRNA基因组非常可能占据非常大的分子空间;因此,假设重要生物病理学现象(即正常发育和与其病理改变的分化)的分子解释是令人逻辑的。

著录项

  • 来源
    《International Journal of Genomics》 |2018年第1期|共2页
  • 作者单位

    Section of Biology and Genetics Giovanni Sichel Department of Biomedical and Biotechnological Sciences University of Catania Catania Italy;

    Section of Philosophical Psychological Pedagogical and Social Sciences Department of Humanities University of Catania Catania Italy;

    Laboratory of Tumor Epigenetics IRCCS AOU San Martino-IST Genova Italy;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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