A subset of conserved mammalian long non-coding RNAs are fossils of ancestral protein-coding genes.
A subset of conserved mammalian long non-coding RNAs are fossils of ancestral protein-coding genes.
复制标题
保守的哺乳动物长的非编码RNA的子集是祖先蛋白质编码基因的化石。
DOI:
10.1186/s13059-017-1293-0
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发表时间:
2017-08-30
期刊:
影响因子:
12.3
通讯作者:
Ulitsky I
中科院分区:
文献类型:
--
作者:
Hezroni H;Ben-Tov Perry R;Meir Z;Housman G;Lubelsky Y;Ulitsky I
Only a small portion of human long non-coding RNAs (lncRNAs) appear to be conserved outside of mammals, but the events underlying the birth of new lncRNAs in mammals remain largely unknown. One potential source is remnants of protein-coding genes that transitioned into lncRNAs. We systematically compare lncRNA and protein-coding loci across vertebrates, and estimate that up to 5% of conserved mammalian lncRNAs are derived from lost protein-coding genes. These lncRNAs have specific characteristics, such as broader expression domains, that set them apart from other lncRNAs. Fourteen lncRNAs have sequence similarity with the loci of the contemporary homologs of the lost protein-coding genes. We propose that selection acting on enhancer sequences is mostly responsible for retention of these regions. As an example of an RNA element from a protein-coding ancestor that was retained in the lncRNA, we describe in detail a short translated ORF in the JPX lncRNA that was derived from an upstream ORF in a protein-coding gene and retains some of its functionality. We estimate that ~ 55 annotated conserved human lncRNAs are derived from parts of ancestral protein-coding genes, and loss of coding potential is thus a non-negligible source of new lncRNAs. Some lncRNAs inherited regulatory elements influencing transcription and translation from their protein-coding ancestors and those elements can influence the expression breadth and functionality of these lncRNAs. The online version of this article (doi:10.1186/s13059-017-1293-0) contains supplementary material, which is available to authorized users.
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