Analysis of secondary structural elements in human microRNA hairpin precursors
MicroRNAs (miRNAs) regulate gene expression by targeting complementary mRNAs for destruction or translational repression. Aberrant expression of miRNAs has been associated with various diseases including cancer, thus making them interesting therapeutic targets. The composite of secondary structural...
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description | MicroRNAs (miRNAs) regulate gene expression by targeting complementary mRNAs for destruction or translational repression. Aberrant expression of miRNAs has been associated with various diseases including cancer, thus making them interesting therapeutic targets. The composite of secondary structural elements that comprise miRNAs could aid the design of small molecules that modulate their function.
We analyzed the secondary structural elements, or motifs, present in all human miRNA hairpin precursors and compared them to highly expressed human RNAs with known structures and other RNAs from various organisms. Amongst human miRNAs, there are 3808 are unique motifs, many residing in processing sites. Further, we identified motifs in miRNAs that are not present in other highly expressed human RNAs, desirable targets for small molecules. MiRNA motifs were incorporated into a searchable database that is freely available. We also analyzed the most frequently occurring bulges and internal loops for each RNA class and found that the smallest loops possible prevail. However, the distribution of loops and the preferred closing base pairs were unique to each class.
Collectively, we have completed a broad survey of motifs found in human miRNA precursors, highly expressed human RNAs, and RNAs from other organisms. Interestingly, unique motifs were identified in human miRNA processing sites, binding to which could inhibit miRNA maturation and hence function. |
doi_str_mv | 10.1186/s12859-016-0960-6 |
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We analyzed the secondary structural elements, or motifs, present in all human miRNA hairpin precursors and compared them to highly expressed human RNAs with known structures and other RNAs from various organisms. Amongst human miRNAs, there are 3808 are unique motifs, many residing in processing sites. Further, we identified motifs in miRNAs that are not present in other highly expressed human RNAs, desirable targets for small molecules. MiRNA motifs were incorporated into a searchable database that is freely available. We also analyzed the most frequently occurring bulges and internal loops for each RNA class and found that the smallest loops possible prevail. However, the distribution of loops and the preferred closing base pairs were unique to each class.
Collectively, we have completed a broad survey of motifs found in human miRNA precursors, highly expressed human RNAs, and RNAs from other organisms. Interestingly, unique motifs were identified in human miRNA processing sites, binding to which could inhibit miRNA maturation and hence function.</description><identifier>ISSN: 1471-2105</identifier><identifier>EISSN: 1471-2105</identifier><identifier>DOI: 10.1186/s12859-016-0960-6</identifier><identifier>PMID: 26928172</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Gene expression ; Gene Expression Regulation ; Humans ; MicroRNA ; MicroRNAs - chemistry ; MicroRNAs - genetics ; Nucleic Acid Conformation ; Nucleotide Motifs - genetics ; RNA Precursors - genetics</subject><ispartof>BMC bioinformatics, 2016-03, Vol.17 (89), p.112-112, Article 112</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>Liu et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-b215ff7f5ee0c6ac57f6c340a7a86df6ca3b8f68d76fb327b389022bf5daa02b3</citedby><cites>FETCH-LOGICAL-c528t-b215ff7f5ee0c6ac57f6c340a7a86df6ca3b8f68d76fb327b389022bf5daa02b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772329/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772329/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26928172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Biao</creatorcontrib><creatorcontrib>Childs-Disney, Jessica L</creatorcontrib><creatorcontrib>Znosko, Brent M</creatorcontrib><creatorcontrib>Wang, Dan</creatorcontrib><creatorcontrib>Fallahi, Mohammad</creatorcontrib><creatorcontrib>Gallo, Steven M</creatorcontrib><creatorcontrib>Disney, Matthew D</creatorcontrib><title>Analysis of secondary structural elements in human microRNA hairpin precursors</title><title>BMC bioinformatics</title><addtitle>BMC Bioinformatics</addtitle><description>MicroRNAs (miRNAs) regulate gene expression by targeting complementary mRNAs for destruction or translational repression. Aberrant expression of miRNAs has been associated with various diseases including cancer, thus making them interesting therapeutic targets. The composite of secondary structural elements that comprise miRNAs could aid the design of small molecules that modulate their function.
We analyzed the secondary structural elements, or motifs, present in all human miRNA hairpin precursors and compared them to highly expressed human RNAs with known structures and other RNAs from various organisms. Amongst human miRNAs, there are 3808 are unique motifs, many residing in processing sites. Further, we identified motifs in miRNAs that are not present in other highly expressed human RNAs, desirable targets for small molecules. MiRNA motifs were incorporated into a searchable database that is freely available. We also analyzed the most frequently occurring bulges and internal loops for each RNA class and found that the smallest loops possible prevail. However, the distribution of loops and the preferred closing base pairs were unique to each class.
Collectively, we have completed a broad survey of motifs found in human miRNA precursors, highly expressed human RNAs, and RNAs from other organisms. Interestingly, unique motifs were identified in human miRNA processing sites, binding to which could inhibit miRNA maturation and hence function.</description><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>MicroRNA</subject><subject>MicroRNAs - chemistry</subject><subject>MicroRNAs - genetics</subject><subject>Nucleic Acid Conformation</subject><subject>Nucleotide Motifs - genetics</subject><subject>RNA Precursors - genetics</subject><issn>1471-2105</issn><issn>1471-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkk1rFTEUhoMotlZ_gBsZcKOLafMxk2Q2wqXYWigtVF2HTCa5N2UmuSYTsf--Z7ht7RXJIoeT53zw5kXoPcHHhEh-kgmVbVdjwmvccVzzF-iQNILUlOD25bP4AL3J-RZjIiRuX6MDyjsqiaCH6GoV9HiXfa6iq7I1MQw63VV5TsXMJemxsqOdbJhz5UO1KZMO1eRNijdXq2qjfdpCepusKSnHlN-iV06P2b57uI_Qz7OvP06_1ZfX5xenq8vatFTOdU9J65xwrbXYcG1a4bhhDdZCSz5ArFkvHZeD4K5nVPRMdpjS3rWD1pj27Ah92fXdln6yg4EFYVe1TX6C9VXUXu2_BL9R6_hbNUJQRjto8OmhQYq_is2zmnw2dhx1sLFkRYSAgUyyBf34D3obSwLZFqoToCMX5C-11qNVPrgIc83SVK2aphG0A_mBOv4PBWewoGoM1nnI7xV83isAZrZ_5rUuOauL7zf7LNmx8D05J-ue9CBYLYZRO8MoMIxaDKM41Hx4LuRTxaND2D2NLLsM</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Liu, Biao</creator><creator>Childs-Disney, Jessica L</creator><creator>Znosko, Brent M</creator><creator>Wang, Dan</creator><creator>Fallahi, Mohammad</creator><creator>Gallo, Steven M</creator><creator>Disney, Matthew D</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7SC</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AL</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0N</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160301</creationdate><title>Analysis of secondary structural elements in human microRNA hairpin precursors</title><author>Liu, Biao ; Childs-Disney, Jessica L ; Znosko, Brent M ; Wang, Dan ; Fallahi, Mohammad ; Gallo, Steven M ; Disney, Matthew D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-b215ff7f5ee0c6ac57f6c340a7a86df6ca3b8f68d76fb327b389022bf5daa02b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>MicroRNA</topic><topic>MicroRNAs - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC bioinformatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Biao</au><au>Childs-Disney, Jessica L</au><au>Znosko, Brent M</au><au>Wang, Dan</au><au>Fallahi, Mohammad</au><au>Gallo, Steven M</au><au>Disney, Matthew D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of secondary structural elements in human microRNA hairpin precursors</atitle><jtitle>BMC bioinformatics</jtitle><addtitle>BMC Bioinformatics</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>17</volume><issue>89</issue><spage>112</spage><epage>112</epage><pages>112-112</pages><artnum>112</artnum><issn>1471-2105</issn><eissn>1471-2105</eissn><abstract>MicroRNAs (miRNAs) regulate gene expression by targeting complementary mRNAs for destruction or translational repression. Aberrant expression of miRNAs has been associated with various diseases including cancer, thus making them interesting therapeutic targets. The composite of secondary structural elements that comprise miRNAs could aid the design of small molecules that modulate their function.
We analyzed the secondary structural elements, or motifs, present in all human miRNA hairpin precursors and compared them to highly expressed human RNAs with known structures and other RNAs from various organisms. Amongst human miRNAs, there are 3808 are unique motifs, many residing in processing sites. Further, we identified motifs in miRNAs that are not present in other highly expressed human RNAs, desirable targets for small molecules. MiRNA motifs were incorporated into a searchable database that is freely available. We also analyzed the most frequently occurring bulges and internal loops for each RNA class and found that the smallest loops possible prevail. However, the distribution of loops and the preferred closing base pairs were unique to each class.
Collectively, we have completed a broad survey of motifs found in human miRNA precursors, highly expressed human RNAs, and RNAs from other organisms. Interestingly, unique motifs were identified in human miRNA processing sites, binding to which could inhibit miRNA maturation and hence function.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26928172</pmid><doi>10.1186/s12859-016-0960-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Springer Nature OA Free Journals; Springer Nature - Complete Springer Journals; PubMed Central |
subjects | Gene expression Gene Expression Regulation Humans MicroRNA MicroRNAs - chemistry MicroRNAs - genetics Nucleic Acid Conformation Nucleotide Motifs - genetics RNA Precursors - genetics |
title | Analysis of secondary structural elements in human microRNA hairpin precursors |
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