Cargando…

Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs

The TATA box represents one of the most prevalent core promoters where the pre-initiation complexes (PICs) for gene transcription are assembled. This assembly is crucial for transcription initiation and well regulated. Here we show that some cellular microRNAs (miRNAs) are associated with RNA polyme...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Yijun, Fan, Miaomiao, Zhang, Xue, Huang, Feng, Wu, Kang, Zhang, Junsong, Liu, Jun, Huang, Zhuoqiong, Luo, Haihua, Tao, Liang, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238354/
https://www.ncbi.nlm.nih.gov/pubmed/25336585
http://dx.doi.org/10.1261/rna.045633.114
_version_ 1782345488880631808
author Zhang, Yijun
Fan, Miaomiao
Zhang, Xue
Huang, Feng
Wu, Kang
Zhang, Junsong
Liu, Jun
Huang, Zhuoqiong
Luo, Haihua
Tao, Liang
Zhang, Hui
author_facet Zhang, Yijun
Fan, Miaomiao
Zhang, Xue
Huang, Feng
Wu, Kang
Zhang, Junsong
Liu, Jun
Huang, Zhuoqiong
Luo, Haihua
Tao, Liang
Zhang, Hui
author_sort Zhang, Yijun
collection PubMed
description The TATA box represents one of the most prevalent core promoters where the pre-initiation complexes (PICs) for gene transcription are assembled. This assembly is crucial for transcription initiation and well regulated. Here we show that some cellular microRNAs (miRNAs) are associated with RNA polymerase II (Pol II) and TATA box-binding protein (TBP) in human peripheral blood mononuclear cells (PBMCs). Among them, let-7i sequence specifically binds to the TATA-box motif of interleukin-2 (IL-2) gene and elevates IL-2 mRNA and protein production in CD4(+) T-lymphocytes in vitro and in vivo. Through direct interaction with the TATA-box motif, let-7i facilitates the PIC assembly and transcription initiation of IL-2 promoter. Several other cellular miRNAs, such as mir-138, mir-92a or mir-181d, also enhance the promoter activities via binding to the TATA-box motifs of insulin, calcitonin or c-myc, respectively. In agreement with the finding that an HIV-1–encoded miRNA could enhance viral replication through targeting the viral promoter TATA-box motif, our data demonstrate that the interaction with core transcription machinery is a novel mechanism for miRNAs to regulate gene expression.
format Online
Article
Text
id pubmed-4238354
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-42383542015-12-01 Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs Zhang, Yijun Fan, Miaomiao Zhang, Xue Huang, Feng Wu, Kang Zhang, Junsong Liu, Jun Huang, Zhuoqiong Luo, Haihua Tao, Liang Zhang, Hui RNA Report The TATA box represents one of the most prevalent core promoters where the pre-initiation complexes (PICs) for gene transcription are assembled. This assembly is crucial for transcription initiation and well regulated. Here we show that some cellular microRNAs (miRNAs) are associated with RNA polymerase II (Pol II) and TATA box-binding protein (TBP) in human peripheral blood mononuclear cells (PBMCs). Among them, let-7i sequence specifically binds to the TATA-box motif of interleukin-2 (IL-2) gene and elevates IL-2 mRNA and protein production in CD4(+) T-lymphocytes in vitro and in vivo. Through direct interaction with the TATA-box motif, let-7i facilitates the PIC assembly and transcription initiation of IL-2 promoter. Several other cellular miRNAs, such as mir-138, mir-92a or mir-181d, also enhance the promoter activities via binding to the TATA-box motifs of insulin, calcitonin or c-myc, respectively. In agreement with the finding that an HIV-1–encoded miRNA could enhance viral replication through targeting the viral promoter TATA-box motif, our data demonstrate that the interaction with core transcription machinery is a novel mechanism for miRNAs to regulate gene expression. Cold Spring Harbor Laboratory Press 2014-12 /pmc/articles/PMC4238354/ /pubmed/25336585 http://dx.doi.org/10.1261/rna.045633.114 Text en © 2014 Zhang et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Report
Zhang, Yijun
Fan, Miaomiao
Zhang, Xue
Huang, Feng
Wu, Kang
Zhang, Junsong
Liu, Jun
Huang, Zhuoqiong
Luo, Haihua
Tao, Liang
Zhang, Hui
Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title_full Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title_fullStr Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title_full_unstemmed Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title_short Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs
title_sort cellular micrornas up-regulate transcription via interaction with promoter tata-box motifs
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238354/
https://www.ncbi.nlm.nih.gov/pubmed/25336585
http://dx.doi.org/10.1261/rna.045633.114
work_keys_str_mv AT zhangyijun cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT fanmiaomiao cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT zhangxue cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT huangfeng cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT wukang cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT zhangjunsong cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT liujun cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT huangzhuoqiong cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT luohaihua cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT taoliang cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs
AT zhanghui cellularmicrornasupregulatetranscriptionviainteractionwithpromotertataboxmotifs