Genome-wide identification of chromatin-enriched RNA reveals that unspliced dentin matrix protein-1 mRNA regulates cell proliferation in squamous cell carcinoma

Chromatin-enriched noncoding RNAs (ncRNAs) have emerged as key molecules in epigenetic processes by interacting with chromatin-associated proteins. Recently, protein-coding mRNA genes have been reported to be chromatin-tethered, similar with ncRNA. However, very little is known about whether chromat...

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Veröffentlicht in:Biochemical and biophysical research communications 2018-01, Vol.495 (3), p.2303-2309
Hauptverfasser: Suzuki, Shigeki, Hoshino, Hiroaki, Yoshida, Kazuma, Nakanishi, Jun, Tsuchiya-Hirata, Shizu, Kobuke, Seiji, Haruyama, Naoto, Nishimura, Fusanori, Shiba, Hideki
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container_title Biochemical and biophysical research communications
container_volume 495
creator Suzuki, Shigeki
Hoshino, Hiroaki
Yoshida, Kazuma
Nakanishi, Jun
Tsuchiya-Hirata, Shizu
Kobuke, Seiji
Haruyama, Naoto
Nishimura, Fusanori
Shiba, Hideki
description Chromatin-enriched noncoding RNAs (ncRNAs) have emerged as key molecules in epigenetic processes by interacting with chromatin-associated proteins. Recently, protein-coding mRNA genes have been reported to be chromatin-tethered, similar with ncRNA. However, very little is known about whether chromatin-enriched mRNA is involved in the chromatin modification process. Here, we comprehensively examined chromatin-enriched RNA in squamous cell carcinoma (SQCC) cells by RNA subcellular localization analysis, which was a combination of RNA fractionation and RNA-seq. We identified 11 mRNAs as highly chromatin-enriched RNAs. Among these, we focused on the dentin matrix protein-1 (DMP-1) gene because its expression in SQCC cells has not been reported. Furthermore, we clarified that DMP-1 mRNA was retained in chromatin in its unspliced form in SQCC in vitro and in vivo. As the inhibition of the unspliced DMP-1 mRNA (unspDMP-1) expression resulted in decreased cellular proliferation in SQCC cells, we performed ChIP-qPCR to identify cell cycle-related genes whose expression was epigenetically modified by unspDMP-1, and found that the CDKN1B promoter became active in SQCC cells by inhibiting unspDMP-1 expression. This result was further validated by the increased CDKN1B gene expression in the cells treated with siRNA for unspDMP-1 and by restoration of the decreased cellular proliferation rate by simultaneously inhibiting CDKN1B expression in SQCC cells. Further, to examine whether unspDMP-1 was able to associate with the CDKN1B promoter region, SQCC cells stably expressing PP7-mCherry fusion protein were transiently transfected with the unspDMP-1 fused to 24 repeats of the PP7 RNA stem loop (unspDMP-1-24xPP7) and we found that unspDMP-1-24xPP7 was efficiently precipitated with the antibody against mCherry and was significantly enriched in the CDKN1B promoter region. Thus, unspDMP-1 is a novel chromatin-enriched RNA that epigenetically regulates cellular proliferation of SQCC. •Subcellular RNA fractionation detected a number of mRNAs bound to chromatin in SQCC.•DMP-1 mRNA was identified as a highly chromatin-enriched mRNA in SQCC.•DMP-1 mRNA existed in an unspliced form in SQCC.•Unspliced DMP-1 mRNA epigenetically modulated proliferative abilities of SQCC.
doi_str_mv 10.1016/j.bbrc.2017.12.136
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Recently, protein-coding mRNA genes have been reported to be chromatin-tethered, similar with ncRNA. However, very little is known about whether chromatin-enriched mRNA is involved in the chromatin modification process. Here, we comprehensively examined chromatin-enriched RNA in squamous cell carcinoma (SQCC) cells by RNA subcellular localization analysis, which was a combination of RNA fractionation and RNA-seq. We identified 11 mRNAs as highly chromatin-enriched RNAs. Among these, we focused on the dentin matrix protein-1 (DMP-1) gene because its expression in SQCC cells has not been reported. Furthermore, we clarified that DMP-1 mRNA was retained in chromatin in its unspliced form in SQCC in vitro and in vivo. As the inhibition of the unspliced DMP-1 mRNA (unspDMP-1) expression resulted in decreased cellular proliferation in SQCC cells, we performed ChIP-qPCR to identify cell cycle-related genes whose expression was epigenetically modified by unspDMP-1, and found that the CDKN1B promoter became active in SQCC cells by inhibiting unspDMP-1 expression. This result was further validated by the increased CDKN1B gene expression in the cells treated with siRNA for unspDMP-1 and by restoration of the decreased cellular proliferation rate by simultaneously inhibiting CDKN1B expression in SQCC cells. Further, to examine whether unspDMP-1 was able to associate with the CDKN1B promoter region, SQCC cells stably expressing PP7-mCherry fusion protein were transiently transfected with the unspDMP-1 fused to 24 repeats of the PP7 RNA stem loop (unspDMP-1-24xPP7) and we found that unspDMP-1-24xPP7 was efficiently precipitated with the antibody against mCherry and was significantly enriched in the CDKN1B promoter region. 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As the inhibition of the unspliced DMP-1 mRNA (unspDMP-1) expression resulted in decreased cellular proliferation in SQCC cells, we performed ChIP-qPCR to identify cell cycle-related genes whose expression was epigenetically modified by unspDMP-1, and found that the CDKN1B promoter became active in SQCC cells by inhibiting unspDMP-1 expression. This result was further validated by the increased CDKN1B gene expression in the cells treated with siRNA for unspDMP-1 and by restoration of the decreased cellular proliferation rate by simultaneously inhibiting CDKN1B expression in SQCC cells. 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Thus, unspDMP-1 is a novel chromatin-enriched RNA that epigenetically regulates cellular proliferation of SQCC. •Subcellular RNA fractionation detected a number of mRNAs bound to chromatin in SQCC.•DMP-1 mRNA was identified as a highly chromatin-enriched mRNA in SQCC.•DMP-1 mRNA existed in an unspliced form in SQCC.•Unspliced DMP-1 mRNA epigenetically modulated proliferative abilities of SQCC.</description><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - genetics</subject><subject>Cellular proliferation</subject><subject>Chromatin - genetics</subject><subject>Chromatin-enriched RNA</subject><subject>Chromosome Mapping - methods</subject><subject>Dentin matrix protein-1</subject><subject>Extracellular Matrix Proteins - genetics</subject><subject>Humans</subject><subject>MicroRNAs - genetics</subject><subject>Phosphoproteins - genetics</subject><subject>RNA subcellular fractionation</subject><subject>RNA, Neoplasm - genetics</subject><subject>RNA, Untranslated - genetics</subject><subject>Squamous cell carcinoma</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1TAQhS1ERS-FF2CBvGST4Jk4fxKbqqIFqQKpAomd5Thjrq_yc2s7Bd6mj4pDLixZWJY155s548PYKxA5CKjeHvKu8yZHAXUOmENRPWE7EK3IEIR8ynZCiCrDFr6ds-chHIQAkFX7jJ1ji3VTi2bHHm9omkfKfrieeDpTdNYZHd088dlys_fzmF5TRpN3Zk89v_t0yT09kB4Cj3sd-TKF4-BMKv3BJ54A737yo58jJRL4uDHfl0FHCtzQMKzVwVny26hEhftFj_NyKhvtjUvO9At2ZtMoenm6L9jX6_dfrj5kt59vPl5d3mamKKuY6Zo6sqhFayWKRhYVFK1sSl2UQsq60h32hG2Htm6krNAAoTS9xQJLaeu2uGBvtr7J2P1CIarRhdWKnii5UtA2IEqJgEmKm9T4OQRPVh29G7X_pUCoNRl1UGsyak1GAaqUTIJen_ov3Uj9P-RvFEnwbhNQ2vLBkVfBOJrSvzpPJqp-dv_r_xuv3KIV</recordid><startdate>20180115</startdate><enddate>20180115</enddate><creator>Suzuki, Shigeki</creator><creator>Hoshino, Hiroaki</creator><creator>Yoshida, Kazuma</creator><creator>Nakanishi, Jun</creator><creator>Tsuchiya-Hirata, Shizu</creator><creator>Kobuke, Seiji</creator><creator>Haruyama, Naoto</creator><creator>Nishimura, Fusanori</creator><creator>Shiba, Hideki</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20180115</creationdate><title>Genome-wide identification of chromatin-enriched RNA reveals that unspliced dentin matrix protein-1 mRNA regulates cell proliferation in squamous cell carcinoma</title><author>Suzuki, Shigeki ; Hoshino, Hiroaki ; Yoshida, Kazuma ; Nakanishi, Jun ; Tsuchiya-Hirata, Shizu ; Kobuke, Seiji ; Haruyama, Naoto ; Nishimura, Fusanori ; Shiba, Hideki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-a7ebef2a09f4208436139485a3504476ab2de29b2f784462c1e24cdf23254f793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - genetics</topic><topic>Cellular proliferation</topic><topic>Chromatin - genetics</topic><topic>Chromatin-enriched RNA</topic><topic>Chromosome Mapping - methods</topic><topic>Dentin matrix protein-1</topic><topic>Extracellular Matrix Proteins - genetics</topic><topic>Humans</topic><topic>MicroRNAs - genetics</topic><topic>Phosphoproteins - genetics</topic><topic>RNA subcellular fractionation</topic><topic>RNA, Neoplasm - genetics</topic><topic>RNA, Untranslated - genetics</topic><topic>Squamous cell carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Shigeki</creatorcontrib><creatorcontrib>Hoshino, Hiroaki</creatorcontrib><creatorcontrib>Yoshida, Kazuma</creatorcontrib><creatorcontrib>Nakanishi, Jun</creatorcontrib><creatorcontrib>Tsuchiya-Hirata, Shizu</creatorcontrib><creatorcontrib>Kobuke, Seiji</creatorcontrib><creatorcontrib>Haruyama, Naoto</creatorcontrib><creatorcontrib>Nishimura, Fusanori</creatorcontrib><creatorcontrib>Shiba, Hideki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Shigeki</au><au>Hoshino, Hiroaki</au><au>Yoshida, Kazuma</au><au>Nakanishi, Jun</au><au>Tsuchiya-Hirata, Shizu</au><au>Kobuke, Seiji</au><au>Haruyama, Naoto</au><au>Nishimura, Fusanori</au><au>Shiba, Hideki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide identification of chromatin-enriched RNA reveals that unspliced dentin matrix protein-1 mRNA regulates cell proliferation in squamous cell carcinoma</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2018-01-15</date><risdate>2018</risdate><volume>495</volume><issue>3</issue><spage>2303</spage><epage>2309</epage><pages>2303-2309</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Chromatin-enriched noncoding RNAs (ncRNAs) have emerged as key molecules in epigenetic processes by interacting with chromatin-associated proteins. Recently, protein-coding mRNA genes have been reported to be chromatin-tethered, similar with ncRNA. However, very little is known about whether chromatin-enriched mRNA is involved in the chromatin modification process. Here, we comprehensively examined chromatin-enriched RNA in squamous cell carcinoma (SQCC) cells by RNA subcellular localization analysis, which was a combination of RNA fractionation and RNA-seq. We identified 11 mRNAs as highly chromatin-enriched RNAs. Among these, we focused on the dentin matrix protein-1 (DMP-1) gene because its expression in SQCC cells has not been reported. Furthermore, we clarified that DMP-1 mRNA was retained in chromatin in its unspliced form in SQCC in vitro and in vivo. As the inhibition of the unspliced DMP-1 mRNA (unspDMP-1) expression resulted in decreased cellular proliferation in SQCC cells, we performed ChIP-qPCR to identify cell cycle-related genes whose expression was epigenetically modified by unspDMP-1, and found that the CDKN1B promoter became active in SQCC cells by inhibiting unspDMP-1 expression. This result was further validated by the increased CDKN1B gene expression in the cells treated with siRNA for unspDMP-1 and by restoration of the decreased cellular proliferation rate by simultaneously inhibiting CDKN1B expression in SQCC cells. Further, to examine whether unspDMP-1 was able to associate with the CDKN1B promoter region, SQCC cells stably expressing PP7-mCherry fusion protein were transiently transfected with the unspDMP-1 fused to 24 repeats of the PP7 RNA stem loop (unspDMP-1-24xPP7) and we found that unspDMP-1-24xPP7 was efficiently precipitated with the antibody against mCherry and was significantly enriched in the CDKN1B promoter region. Thus, unspDMP-1 is a novel chromatin-enriched RNA that epigenetically regulates cellular proliferation of SQCC. •Subcellular RNA fractionation detected a number of mRNAs bound to chromatin in SQCC.•DMP-1 mRNA was identified as a highly chromatin-enriched mRNA in SQCC.•DMP-1 mRNA existed in an unspliced form in SQCC.•Unspliced DMP-1 mRNA epigenetically modulated proliferative abilities of SQCC.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29278708</pmid><doi>10.1016/j.bbrc.2017.12.136</doi><tpages>7</tpages></addata></record>
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subjects Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - metabolism
Carcinoma, Squamous Cell - pathology
Cell Line, Tumor
Cell Proliferation - genetics
Cellular proliferation
Chromatin - genetics
Chromatin-enriched RNA
Chromosome Mapping - methods
Dentin matrix protein-1
Extracellular Matrix Proteins - genetics
Humans
MicroRNAs - genetics
Phosphoproteins - genetics
RNA subcellular fractionation
RNA, Neoplasm - genetics
RNA, Untranslated - genetics
Squamous cell carcinoma
title Genome-wide identification of chromatin-enriched RNA reveals that unspliced dentin matrix protein-1 mRNA regulates cell proliferation in squamous cell carcinoma
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