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        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDA34559</PRIMARY_ID>
        </IDENTIFIERS>
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            <STUDY_TITLE>RNA stability defines the identity of long noncoding RNA in mammals</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
            <STUDY_ABSTRACT>There is growing recognition that mammalian genomes produce huge number of long noncoding RNAs (ncRNAs). However, the biological functions of most long ncRNAs are still unclear. Here we report a new approach to uncover the discriminative property of the functional long ncRNAs by combination of comprehensively measuring the half-lives and functional analysis. Our approach reveals hundreds of short-lived ncRNAs in which many well-known functional long ncRNAs are sorted. Moreover, we provide strong evidence that modulation of half-lives of relatively short-lived functional long ncRNAs, viz. NEAT1/MEN ⋯ and GAS5, alters functional consequence, and identified novel short-lived intergenic noncoding transcripts (SLITs), those degradations are regulated by stimuli, involving in cell proliferation. Together, these results propose that short-lived property of ncRNA will be key parameter for identifying the uncharacterized long ncRNAs.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>Integrateve Transcriptome Analysis</CENTER_PROJECT_NAME>
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                        <DB>bioproject</DB>
                        <ID>PRJDA34559</ID>
                        <LABEL>PRJDA34559</LABEL>
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                    <IS_PRIMARY>true</IS_PRIMARY>
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                <RELATED_STUDY>
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                        <DB>genomeprj</DB>
                        <ID>34559</ID>
                        <LABEL>34559</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>false</IS_PRIMARY>
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            <STUDY_DESCRIPTION>There is growing recognition that mammalian genomes produce huge number of long noncoding RNAs (ncRNAs). However, the biological functions of most long ncRNAs are still unclear. Here we report a new approach to uncover the discriminative property of the functional long ncRNAs by combination of comprehensively measuring the half-lives and functional analysis. Our approach reveals hundreds of short-lived ncRNAs in which many well-known functional long ncRNAs are sorted. Moreover, we provide strong evidence that modulation of half-lives of relatively short-lived functional long ncRNAs, viz. NEAT1/MEN ⋯ and GAS5, alters functional consequence, and identified novel short-lived intergenic noncoding transcripts (SLITs), those degradations are regulated by stimuli, involving in cell proliferation. Together, these results propose that short-lived property of ncRNA will be key parameter for identifying the uncharacterized long ncRNAs.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
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