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NF90 in posttranscriptional gene regulation and microRNA biogenesis
Gene expression patterns are effectively regulated by turnover and translation regulatory (TTR) RNA-binding proteins (RBPs). The TTR-RBPs control gene expression at posttranscriptional levels, such as pre-mRNA splicing, mRNA cytoplasmic export, turnover, storage, and translation. Double-stranded RNA...
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Published in: | International Journal of Molecular Sciences 2013-08, Vol.14 (8), p.17111-17121 |
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creator | Masuda, Kiyoshi Kuwano, Yuki Nishida, Kensei Rokutan, Kazuhito Imoto, Issei |
description | Gene expression patterns are effectively regulated by turnover and translation regulatory (TTR) RNA-binding proteins (RBPs). The TTR-RBPs control gene expression at posttranscriptional levels, such as pre-mRNA splicing, mRNA cytoplasmic export, turnover, storage, and translation. Double-stranded RNA binding proteins (DSRBPs) are known to regulate many processes of cellular metabolism, including transcriptional control, translational control, mRNA processing and localization. Nuclear factor 90 (NF90), one of the DSRBPs, is abundantly expressed in vertebrate tissue and participates in many aspects of RNA metabolism. NF90 was originally purified as a component of a DNA binding complex which binds to the antigen recognition response element 2 in the interleukin 2 promoter. Recent studies have provided us with interesting insights into its possible physiological roles in RNA metabolism, including transcription, degradation, and translation. In addition, it was shown that NF90 regulates microRNA expression. In this review, we try to focus on the function of NF90 in posttranscriptional gene regulation and microRNA biogenesis. |
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The TTR-RBPs control gene expression at posttranscriptional levels, such as pre-mRNA splicing, mRNA cytoplasmic export, turnover, storage, and translation. Double-stranded RNA binding proteins (DSRBPs) are known to regulate many processes of cellular metabolism, including transcriptional control, translational control, mRNA processing and localization. Nuclear factor 90 (NF90), one of the DSRBPs, is abundantly expressed in vertebrate tissue and participates in many aspects of RNA metabolism. NF90 was originally purified as a component of a DNA binding complex which binds to the antigen recognition response element 2 in the interleukin 2 promoter. Recent studies have provided us with interesting insights into its possible physiological roles in RNA metabolism, including transcription, degradation, and translation. In addition, it was shown that NF90 regulates microRNA expression. 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The TTR-RBPs control gene expression at posttranscriptional levels, such as pre-mRNA splicing, mRNA cytoplasmic export, turnover, storage, and translation. Double-stranded RNA binding proteins (DSRBPs) are known to regulate many processes of cellular metabolism, including transcriptional control, translational control, mRNA processing and localization. Nuclear factor 90 (NF90), one of the DSRBPs, is abundantly expressed in vertebrate tissue and participates in many aspects of RNA metabolism. NF90 was originally purified as a component of a DNA binding complex which binds to the antigen recognition response element 2 in the interleukin 2 promoter. Recent studies have provided us with interesting insights into its possible physiological roles in RNA metabolism, including transcription, degradation, and translation. In addition, it was shown that NF90 regulates microRNA expression. In this review, we try to focus on the function of NF90 in posttranscriptional gene regulation and microRNA biogenesis.</description><subject>Animals</subject><subject>double-stranded RNA binding proteins</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>microRNA biogenesis</subject><subject>MicroRNAs - biosynthesis</subject><subject>MicroRNAs - genetics</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - metabolism</subject><subject>NF90</subject><subject>Nuclear Factor 90 Proteins - physiology</subject><subject>posttranscriptional regulation</subject><subject>Protein Biosynthesis</subject><subject>Review</subject><subject>RNA Interference</subject><subject>RNA Stability</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFks1LHTEUxUNpUWtddlsGunEzbb4z2QjyqK0gCqLrkLnJvOYxM3kmM4X-9834rPjcuEq458fhXO5B6DPB3xjT-HvYDJlw3BBFCHmHjgintMZYqvcv_ofoY84bjCmjQh-gQ8q0FFqJI7S6vtC4CmO1jXmakh0zpLCdQhxtX6396Kvk13Nvl0llR1cNAVK8vT6v2hAXPYf8CX3obJ_9ydN7jO4vftytftVXNz8vV-dXNYgGT7VmQF3T2RY8BS4b0JY3wssiattZ4JpLImgnWyqYBMcVAxAKU9Ew3jnOjtHlztdFuzHbFAab_ppog3kcxLQ2Nk0Bem9023YCGgDnJCfYtthqrmTHJNYOqC1eZzuv7dwO3oEfy_L9num-MobfZh3_GKaE1mIJc_pkkOLD7PNkhpDB970dfZyzIYoqqUt49jbKqVIcc6EK-vUVuolzKrcolKCSNpSQxbDeUeUUOSffPecm2CytMHutKPyXl8s-0_9rwP4B6zyyWg</recordid><startdate>20130819</startdate><enddate>20130819</enddate><creator>Masuda, Kiyoshi</creator><creator>Kuwano, Yuki</creator><creator>Nishida, Kensei</creator><creator>Rokutan, Kazuhito</creator><creator>Imoto, Issei</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130819</creationdate><title>NF90 in posttranscriptional gene regulation and microRNA biogenesis</title><author>Masuda, Kiyoshi ; 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The TTR-RBPs control gene expression at posttranscriptional levels, such as pre-mRNA splicing, mRNA cytoplasmic export, turnover, storage, and translation. Double-stranded RNA binding proteins (DSRBPs) are known to regulate many processes of cellular metabolism, including transcriptional control, translational control, mRNA processing and localization. Nuclear factor 90 (NF90), one of the DSRBPs, is abundantly expressed in vertebrate tissue and participates in many aspects of RNA metabolism. NF90 was originally purified as a component of a DNA binding complex which binds to the antigen recognition response element 2 in the interleukin 2 promoter. Recent studies have provided us with interesting insights into its possible physiological roles in RNA metabolism, including transcription, degradation, and translation. In addition, it was shown that NF90 regulates microRNA expression. 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subjects | Animals double-stranded RNA binding proteins Gene Expression Regulation, Neoplastic Humans microRNA biogenesis MicroRNAs - biosynthesis MicroRNAs - genetics Neoplasms - genetics Neoplasms - metabolism NF90 Nuclear Factor 90 Proteins - physiology posttranscriptional regulation Protein Biosynthesis Review RNA Interference RNA Stability RNA, Messenger - genetics RNA, Messenger - metabolism |
title | NF90 in posttranscriptional gene regulation and microRNA biogenesis |
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