New class of gene-termini-associated human RNAs suggests a novel RNA copying mechanism.
New class of gene-termini-associated human RNAs suggests a novel RNA copying mechanism.
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Short (< 200 nt) RNA (sRNA) profiling of human cells using various technologies demonstrates unexpected complexity of sRNAs with 100’s of thousands of sRNA species present. Genetic and in vitro studies argue that these RNAs are not merely degradation products of longer transcripts but could indeed have function. Furthermore, profiling of RNAs, including the sRNAs, can reveal not only novel transcripts, but also make clear predictions about the existence and properties of novel biochemical pathways operating in a cell. For example, short RNA profiling in human cells suggested existence of an unknown capping mechanism operating on cleaved RNA a biochemical component of which was later identified. Here we show that human cells contain a novel type of sRNAs that have non-genomically encoded 5’ polyU tails. Presence of these RNAs at the termini of genes, specifically at the very 3’ ends of known mRNAs strongly argues for the presence of a yet uncharacterized endogenous biochemical pathway in a cell that can copy RNA. We show that this pathway can operate on multiple genes, with specific enrichment towards transcripts encoding components of the translational machinery. Finally we show that genes are also flanked by sense, 3’ polyadenylated sRNAs that are likely to be capped.
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影响因子:
64.8
作者:
通讯作者:
--
DOI:
10.1126/science.1162253
发表时间:
2008-12-19
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Seila AC;Calabrese JM;Levine SS;Yeo GW;Rahl PB;Flynn RA;Young RA;Sharp PA
通讯作者:
Sharp PA
影响因子:
56.9
作者:
Kapranov, Philipp;Cheng, Jill;Gingeras, Thomas R.
通讯作者:
Gingeras, Thomas R.
DOI:
10.1073/pnas.93.6.2476
发表时间:
1996-03-19
影响因子:
11.1
作者:
Volloch, V;Schweitzer, B;Rits, S
通讯作者:
Rits, S
影响因子:
64.8
作者:
Rassoulzadegan, Minoo;Grandjean, Valerie;Cuzin, Francois
通讯作者:
Cuzin, Francois