Telomerase Reverse Transcriptase Regulates microRNAs
MicroRNAs are small non-coding RNAs that inhibit the translation of target mRNAs. In humans, most microRNAs are transcribed by RNA polymerase II as long primary transcripts and processed by sequential cleavage of the two RNase III enzymes, DROSHA and DICER, into precursor and mature microRNAs, respe...
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pubmed-43072982015-02-02 Telomerase Reverse Transcriptase Regulates microRNAs Lassmann, Timo Maida, Yoshiko Tomaru, Yasuhiro Yasukawa, Mami Ando, Yoshinari Kojima, Miki Kasim, Vivi Simon, Christophe Daub, Carsten O. Carninci, Piero Hayashizaki, Yoshihide Masutomi, Kenkichi Article MicroRNAs are small non-coding RNAs that inhibit the translation of target mRNAs. In humans, most microRNAs are transcribed by RNA polymerase II as long primary transcripts and processed by sequential cleavage of the two RNase III enzymes, DROSHA and DICER, into precursor and mature microRNAs, respectively. Although the fundamental functions of microRNAs in RNA silencing have been gradually uncovered, less is known about the regulatory mechanisms of microRNA expression. Here, we report that telomerase reverse transcriptase (TERT) extensively affects the expression levels of mature microRNAs. Deep sequencing-based screens of short RNA populations revealed that the suppression of TERT resulted in the downregulation of microRNAs expressed in THP-1 cells and HeLa cells. Primary and precursor microRNA levels were also reduced under the suppression of TERT. Similar results were obtained with the suppression of either BRG1 (also called SMARCA4) or nucleostemin, which are proteins interacting with TERT and functioning beyond telomeres. These results suggest that TERT regulates microRNAs at the very early phases in their biogenesis, presumably through non-telomerase mechanism(s). MDPI 2015-01-06 /pmc/articles/PMC4307298/ /pubmed/25569094 http://dx.doi.org/10.3390/ijms16011192 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Lassmann, Timo Maida, Yoshiko Tomaru, Yasuhiro Yasukawa, Mami Ando, Yoshinari Kojima, Miki Kasim, Vivi Simon, Christophe Daub, Carsten O. Carninci, Piero Hayashizaki, Yoshihide Masutomi, Kenkichi |
spellingShingle |
Lassmann, Timo Maida, Yoshiko Tomaru, Yasuhiro Yasukawa, Mami Ando, Yoshinari Kojima, Miki Kasim, Vivi Simon, Christophe Daub, Carsten O. Carninci, Piero Hayashizaki, Yoshihide Masutomi, Kenkichi Telomerase Reverse Transcriptase Regulates microRNAs |
author_facet |
Lassmann, Timo Maida, Yoshiko Tomaru, Yasuhiro Yasukawa, Mami Ando, Yoshinari Kojima, Miki Kasim, Vivi Simon, Christophe Daub, Carsten O. Carninci, Piero Hayashizaki, Yoshihide Masutomi, Kenkichi |
author_sort |
Lassmann, Timo |
title |
Telomerase Reverse Transcriptase Regulates microRNAs |
title_short |
Telomerase Reverse Transcriptase Regulates microRNAs |
title_full |
Telomerase Reverse Transcriptase Regulates microRNAs |
title_fullStr |
Telomerase Reverse Transcriptase Regulates microRNAs |
title_full_unstemmed |
Telomerase Reverse Transcriptase Regulates microRNAs |
title_sort |
telomerase reverse transcriptase regulates micrornas |
description |
MicroRNAs are small non-coding RNAs that inhibit the translation of target mRNAs. In humans, most microRNAs are transcribed by RNA polymerase II as long primary transcripts and processed by sequential cleavage of the two RNase III enzymes, DROSHA and DICER, into precursor and mature microRNAs, respectively. Although the fundamental functions of microRNAs in RNA silencing have been gradually uncovered, less is known about the regulatory mechanisms of microRNA expression. Here, we report that telomerase reverse transcriptase (TERT) extensively affects the expression levels of mature microRNAs. Deep sequencing-based screens of short RNA populations revealed that the suppression of TERT resulted in the downregulation of microRNAs expressed in THP-1 cells and HeLa cells. Primary and precursor microRNA levels were also reduced under the suppression of TERT. Similar results were obtained with the suppression of either BRG1 (also called SMARCA4) or nucleostemin, which are proteins interacting with TERT and functioning beyond telomeres. These results suggest that TERT regulates microRNAs at the very early phases in their biogenesis, presumably through non-telomerase mechanism(s). |
publisher |
MDPI |
publishDate |
2015 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307298/ |
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1613181026094284800 |