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miRNA-mediated functional changes through co-regulating function related genes
MicroRNAs play important roles in various biological processes involving fairly complex mechanism. Analysis of genome-wide miRNA microarray demonstrate that a single miRNA can regulate hundreds of genes, but the regulative extent on most individual genes is surprisingly mild so that it is difficult...
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Published in: | PloS one 2010-10, Vol.5 (10), p.e13558-e13558 |
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description | MicroRNAs play important roles in various biological processes involving fairly complex mechanism. Analysis of genome-wide miRNA microarray demonstrate that a single miRNA can regulate hundreds of genes, but the regulative extent on most individual genes is surprisingly mild so that it is difficult to understand how a miRNA provokes detectable functional changes with such mild regulation.
To explore the internal mechanism of miRNA-mediated regulation, we re-analyzed the data collected from genome-wide miRNA microarray with bioinformatics assay, and found that the transfection of miR-181b and miR-34a in Hela and HCT-116 tumor cells regulated large numbers of genes, among which, the genes related to cell growth and cell death demonstrated high Enrichment scores, suggesting that these miRNAs may be important in cell growth and cell death. MiR-181b induced changes in protein expression of most genes that were seemingly related to enhancing cell growth and decreasing cell death, while miR-34a mediated contrary changes of gene expression. Cell growth assays further confirmed this finding. In further study on miR-20b-mediated osteogenesis in hMSCs, miR-20b was found to enhance osteogenesis by activating BMPs/Runx2 signaling pathway in several stages by co-repressing of PPARγ, Bambi and Crim1.
With its multi-target characteristics, miR-181b, miR-34a and miR-20b provoked detectable functional changes by co-regulating functionally-related gene groups or several genes in the same signaling pathway, and thus mild regulation from individual miRNA targeting genes could have contributed to an additive effect. This might also be one of the modes of miRNA-mediated gene regulation. |
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To explore the internal mechanism of miRNA-mediated regulation, we re-analyzed the data collected from genome-wide miRNA microarray with bioinformatics assay, and found that the transfection of miR-181b and miR-34a in Hela and HCT-116 tumor cells regulated large numbers of genes, among which, the genes related to cell growth and cell death demonstrated high Enrichment scores, suggesting that these miRNAs may be important in cell growth and cell death. MiR-181b induced changes in protein expression of most genes that were seemingly related to enhancing cell growth and decreasing cell death, while miR-34a mediated contrary changes of gene expression. Cell growth assays further confirmed this finding. In further study on miR-20b-mediated osteogenesis in hMSCs, miR-20b was found to enhance osteogenesis by activating BMPs/Runx2 signaling pathway in several stages by co-repressing of PPARγ, Bambi and Crim1.
With its multi-target characteristics, miR-181b, miR-34a and miR-20b provoked detectable functional changes by co-regulating functionally-related gene groups or several genes in the same signaling pathway, and thus mild regulation from individual miRNA targeting genes could have contributed to an additive effect. This might also be one of the modes of miRNA-mediated gene regulation.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0013558</identifier><identifier>PMID: 21042576</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>3' Untranslated Regions ; Apoptosis ; Base Sequence ; Biochemistry/Transcription and Translation ; Biocompatibility ; Bioinformatics ; Biological activity ; Biomedical materials ; Cbfa-1 protein ; Cell Biology ; Cell Biology/Cell Signaling ; Cell death ; Cell growth ; Cell Line, Tumor ; Change detection ; Data processing ; DNA microarrays ; Enzyme-Linked Immunosorbent Assay ; Gene expression ; Gene Expression Regulation ; Gene regulation ; Genes ; Genetic research ; Genetics and Genomics/Gene Expression ; Genomes ; Genomics ; Health sciences ; Humans ; Life sciences ; MicroRNA ; MicroRNAs ; MicroRNAs - physiology ; miRNA ; Molecular Biology/Translational Regulation ; Mortality ; Osteogenesis ; Proteins ; Ribonucleic acid ; RNA ; Signal Transduction ; Signaling ; Stem cells ; Transfection ; Tumor cells</subject><ispartof>PloS one, 2010-10, Vol.5 (10), p.e13558-e13558</ispartof><rights>COPYRIGHT 2010 Public Library of Science</rights><rights>2010 He et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>He et al. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c723t-624fcd40f382668512b19e048faf98a13c5ab2e47916438c85d82514e9dabcbf3</citedby><cites>FETCH-LOGICAL-c723t-624fcd40f382668512b19e048faf98a13c5ab2e47916438c85d82514e9dabcbf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1292301331/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1292301331?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21042576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kashanchi, Fatah</contributor><creatorcontrib>He, Jie</creatorcontrib><creatorcontrib>Zhang, Jin-fang</creatorcontrib><creatorcontrib>Yi, Can</creatorcontrib><creatorcontrib>Lv, Qing</creatorcontrib><creatorcontrib>Xie, Wei-dong</creatorcontrib><creatorcontrib>Li, Jian-na</creatorcontrib><creatorcontrib>Wan, Gang</creatorcontrib><creatorcontrib>Cui, Kai</creatorcontrib><creatorcontrib>Kung, Hsiang-fu</creatorcontrib><creatorcontrib>Yang, Jennifer</creatorcontrib><creatorcontrib>Yang, Burton B</creatorcontrib><creatorcontrib>Zhang, Yaou</creatorcontrib><title>miRNA-mediated functional changes through co-regulating function related genes</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>MicroRNAs play important roles in various biological processes involving fairly complex mechanism. Analysis of genome-wide miRNA microarray demonstrate that a single miRNA can regulate hundreds of genes, but the regulative extent on most individual genes is surprisingly mild so that it is difficult to understand how a miRNA provokes detectable functional changes with such mild regulation.
To explore the internal mechanism of miRNA-mediated regulation, we re-analyzed the data collected from genome-wide miRNA microarray with bioinformatics assay, and found that the transfection of miR-181b and miR-34a in Hela and HCT-116 tumor cells regulated large numbers of genes, among which, the genes related to cell growth and cell death demonstrated high Enrichment scores, suggesting that these miRNAs may be important in cell growth and cell death. MiR-181b induced changes in protein expression of most genes that were seemingly related to enhancing cell growth and decreasing cell death, while miR-34a mediated contrary changes of gene expression. Cell growth assays further confirmed this finding. In further study on miR-20b-mediated osteogenesis in hMSCs, miR-20b was found to enhance osteogenesis by activating BMPs/Runx2 signaling pathway in several stages by co-repressing of PPARγ, Bambi and Crim1.
With its multi-target characteristics, miR-181b, miR-34a and miR-20b provoked detectable functional changes by co-regulating functionally-related gene groups or several genes in the same signaling pathway, and thus mild regulation from individual miRNA targeting genes could have contributed to an additive effect. This might also be one of the modes of miRNA-mediated gene regulation.</description><subject>3' Untranslated Regions</subject><subject>Apoptosis</subject><subject>Base Sequence</subject><subject>Biochemistry/Transcription and Translation</subject><subject>Biocompatibility</subject><subject>Bioinformatics</subject><subject>Biological activity</subject><subject>Biomedical materials</subject><subject>Cbfa-1 protein</subject><subject>Cell Biology</subject><subject>Cell Biology/Cell Signaling</subject><subject>Cell death</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Change detection</subject><subject>Data processing</subject><subject>DNA microarrays</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Gene regulation</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Genetics and Genomics/Gene Expression</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health sciences</subject><subject>Humans</subject><subject>Life sciences</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - physiology</subject><subject>miRNA</subject><subject>Molecular Biology/Translational Regulation</subject><subject>Mortality</subject><subject>Osteogenesis</subject><subject>Proteins</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Signal Transduction</subject><subject>Signaling</subject><subject>Stem cells</subject><subject>Transfection</subject><subject>Tumor cells</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11r2zAUhs3YWNts_2BsgcHGLpJZn5ZvBqHsI1Ba6D5uhSIf2QqKlUn2WP_9lMQN8Shs-MJGft5XR-_RybIXKJ8jUqD3a9-HVrn51rcwz3NEGBOPsnNUEjzjOCePT77PsosY13nOiOD8aXaGUU4xK_h5dr2xt9eL2QYqqzqopqZvdWd9Mp7qRrU1xGnXBN_XzVT7WYC6d6qzbX0EpwHcXllDC_FZ9sQoF-H58J5k3z99_Hb5ZXZ183l5ubia6QKTLtVEja5obojAnAuG8AqVkFNhlCmFQkQztcJAixJxSoQWrBKYIQplpVZ6Zcgke3Xw3Tof5RBFlAiXmKQoCErE8kBUXq3lNtiNCnfSKyv3Cz7UUoXOageSKMOwYrRkBihUQmDKSwZCp5oqVtDk9WHYrV-lpDS0XVBuZDr-09pG1v6XxCXHfF_M28Eg-J89xE5ubNTgnGrB91EKnjZP3SH_JAuOsaCkKBL5-i_y4RgGqlbppLY1PhWod55yQQuSrFjqyCSbP0Clp4KN1emCGZvWR4J3I0FiOvjd1aqPUS6_3v4_e_NjzL45YRtQrmuid_3upsUxSA-gDj7GAObYDZTL3XzcpyF38yGH-Uiyl6edPIruB4L8AVqZCZM</recordid><startdate>20101022</startdate><enddate>20101022</enddate><creator>He, Jie</creator><creator>Zhang, Jin-fang</creator><creator>Yi, Can</creator><creator>Lv, Qing</creator><creator>Xie, Wei-dong</creator><creator>Li, Jian-na</creator><creator>Wan, Gang</creator><creator>Cui, Kai</creator><creator>Kung, Hsiang-fu</creator><creator>Yang, Jennifer</creator><creator>Yang, Burton B</creator><creator>Zhang, Yaou</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20101022</creationdate><title>miRNA-mediated functional changes through co-regulating function related genes</title><author>He, Jie ; Zhang, Jin-fang ; Yi, Can ; Lv, Qing ; Xie, Wei-dong ; Li, Jian-na ; Wan, Gang ; Cui, Kai ; Kung, Hsiang-fu ; Yang, Jennifer ; Yang, Burton B ; Zhang, Yaou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c723t-624fcd40f382668512b19e048faf98a13c5ab2e47916438c85d82514e9dabcbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>3' Untranslated Regions</topic><topic>Apoptosis</topic><topic>Base Sequence</topic><topic>Biochemistry/Transcription and Translation</topic><topic>Biocompatibility</topic><topic>Bioinformatics</topic><topic>Biological activity</topic><topic>Biomedical materials</topic><topic>Cbfa-1 protein</topic><topic>Cell Biology</topic><topic>Cell Biology/Cell Signaling</topic><topic>Cell death</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Change detection</topic><topic>Data processing</topic><topic>DNA microarrays</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Gene regulation</topic><topic>Genes</topic><topic>Genetic research</topic><topic>Genetics and Genomics/Gene Expression</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health sciences</topic><topic>Humans</topic><topic>Life sciences</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>MicroRNAs - 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Analysis of genome-wide miRNA microarray demonstrate that a single miRNA can regulate hundreds of genes, but the regulative extent on most individual genes is surprisingly mild so that it is difficult to understand how a miRNA provokes detectable functional changes with such mild regulation.
To explore the internal mechanism of miRNA-mediated regulation, we re-analyzed the data collected from genome-wide miRNA microarray with bioinformatics assay, and found that the transfection of miR-181b and miR-34a in Hela and HCT-116 tumor cells regulated large numbers of genes, among which, the genes related to cell growth and cell death demonstrated high Enrichment scores, suggesting that these miRNAs may be important in cell growth and cell death. MiR-181b induced changes in protein expression of most genes that were seemingly related to enhancing cell growth and decreasing cell death, while miR-34a mediated contrary changes of gene expression. Cell growth assays further confirmed this finding. In further study on miR-20b-mediated osteogenesis in hMSCs, miR-20b was found to enhance osteogenesis by activating BMPs/Runx2 signaling pathway in several stages by co-repressing of PPARγ, Bambi and Crim1.
With its multi-target characteristics, miR-181b, miR-34a and miR-20b provoked detectable functional changes by co-regulating functionally-related gene groups or several genes in the same signaling pathway, and thus mild regulation from individual miRNA targeting genes could have contributed to an additive effect. This might also be one of the modes of miRNA-mediated gene regulation.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21042576</pmid><doi>10.1371/journal.pone.0013558</doi><tpages>e13558</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated Regions Apoptosis Base Sequence Biochemistry/Transcription and Translation Biocompatibility Bioinformatics Biological activity Biomedical materials Cbfa-1 protein Cell Biology Cell Biology/Cell Signaling Cell death Cell growth Cell Line, Tumor Change detection Data processing DNA microarrays Enzyme-Linked Immunosorbent Assay Gene expression Gene Expression Regulation Gene regulation Genes Genetic research Genetics and Genomics/Gene Expression Genomes Genomics Health sciences Humans Life sciences MicroRNA MicroRNAs MicroRNAs - physiology miRNA Molecular Biology/Translational Regulation Mortality Osteogenesis Proteins Ribonucleic acid RNA Signal Transduction Signaling Stem cells Transfection Tumor cells |
title | miRNA-mediated functional changes through co-regulating function related genes |
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