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High-throughput microarray reveals the epitranscriptome-wide landscape of m6A-modified circRNA in oral squamous cell carcinoma
Emerging transcriptome-wide high-throughput screenings reveal the landscape and functions of RNAs, such as circular RNAs (circRNAs), in human cancer. In addition, the post-transcriptional RNA internal modifications, especially N.sup.6-methyladenosine (m.sup.6A), greatly enrich the variety of RNAs me...
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Published in: | BMC genomics 2022-08, Vol.23 (1), p.1-611, Article 611 |
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description | Emerging transcriptome-wide high-throughput screenings reveal the landscape and functions of RNAs, such as circular RNAs (circRNAs), in human cancer. In addition, the post-transcriptional RNA internal modifications, especially N.sup.6-methyladenosine (m.sup.6A), greatly enrich the variety of RNAs metabolism. However, the m.sup.6A modification on circRNAs has yet to be addressed. Here, we report an epitranscriptome-wide mapping of m.sup.6A-modified circRNAs (m.sup.6A-circRNA) in oral squamous cell carcinoma (OSCC). Utilizing the data of m.sup.6A methylated RNA immunoprecipitation sequencing (MeRIP-seq) and m.sup.6A-circRNAs microarray, we found that m.sup.6A-circRNAs exhibited particular modification styles in OSCC, which was independent of m.sup.6A-mRNA. Besides, m.sup.6A modification on circRNAs frequently occurred on the long exons in the front part of the coding sequence (CDS), which was distinct from m.sup.6A-mRNA that in 3'-UTR or stop codon. In conclusion, our work preliminarily demonstrates the traits of m.sup.6A-circRNAs, which may bring enlighten for the roles of m.sup.6A-circRNAs in OSCC. |
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In addition, the post-transcriptional RNA internal modifications, especially N.sup.6-methyladenosine (m.sup.6A), greatly enrich the variety of RNAs metabolism. However, the m.sup.6A modification on circRNAs has yet to be addressed. Here, we report an epitranscriptome-wide mapping of m.sup.6A-modified circRNAs (m.sup.6A-circRNA) in oral squamous cell carcinoma (OSCC). Utilizing the data of m.sup.6A methylated RNA immunoprecipitation sequencing (MeRIP-seq) and m.sup.6A-circRNAs microarray, we found that m.sup.6A-circRNAs exhibited particular modification styles in OSCC, which was independent of m.sup.6A-mRNA. Besides, m.sup.6A modification on circRNAs frequently occurred on the long exons in the front part of the coding sequence (CDS), which was distinct from m.sup.6A-mRNA that in 3'-UTR or stop codon. In conclusion, our work preliminarily demonstrates the traits of m.sup.6A-circRNAs, which may bring enlighten for the roles of m.sup.6A-circRNAs in OSCC.</description><identifier>ISSN: 1471-2164</identifier><identifier>EISSN: 1471-2164</identifier><identifier>DOI: 10.1186/s12864-022-08806-z</identifier><identifier>PMID: 35999496</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>3' Untranslated regions ; Cancer ; Circular RNA ; Diagnosis ; Enzymes ; Exons ; Gene sequencing ; Genes ; Genetic aspects ; Genetic transcription ; Genomics ; Health aspects ; Immunoprecipitation ; m6A-circRNAs ; Medical prognosis ; MeRIP-Seq ; N6-Methyladenosine ; Oral cancer ; Oral carcinoma ; Oral squamous cell carcinoma ; Post-transcription ; RNA ; RNA modification ; Squamous cell carcinoma ; Stop codon ; Transcriptomes ; Tumorigenesis</subject><ispartof>BMC genomics, 2022-08, Vol.23 (1), p.1-611, Article 611</ispartof><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-82fd5b542ea3b2bbfc0782bf3f190bc3d1990bae516362aef37ed379d5371cf93</citedby><cites>FETCH-LOGICAL-c504t-82fd5b542ea3b2bbfc0782bf3f190bc3d1990bae516362aef37ed379d5371cf93</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/PMC9400228/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2715425956?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids></links><search><creatorcontrib>Zhao, Wei</creatorcontrib><creatorcontrib>Liu, Jingwen</creatorcontrib><creatorcontrib>Wu, Jie</creatorcontrib><creatorcontrib>Ma, Xiaozhou</creatorcontrib><creatorcontrib>Wang, Xi</creatorcontrib><creatorcontrib>Zhang, Leyu</creatorcontrib><creatorcontrib>Han, Zhe</creatorcontrib><creatorcontrib>Yang, Jianming</creatorcontrib><creatorcontrib>Cui, Yameng</creatorcontrib><creatorcontrib>Hu, Xin</creatorcontrib><creatorcontrib>Deng, Jiayin</creatorcontrib><title>High-throughput microarray reveals the epitranscriptome-wide landscape of m6A-modified circRNA in oral squamous cell carcinoma</title><title>BMC genomics</title><description>Emerging transcriptome-wide high-throughput screenings reveal the landscape and functions of RNAs, such as circular RNAs (circRNAs), in human cancer. In addition, the post-transcriptional RNA internal modifications, especially N.sup.6-methyladenosine (m.sup.6A), greatly enrich the variety of RNAs metabolism. However, the m.sup.6A modification on circRNAs has yet to be addressed. Here, we report an epitranscriptome-wide mapping of m.sup.6A-modified circRNAs (m.sup.6A-circRNA) in oral squamous cell carcinoma (OSCC). Utilizing the data of m.sup.6A methylated RNA immunoprecipitation sequencing (MeRIP-seq) and m.sup.6A-circRNAs microarray, we found that m.sup.6A-circRNAs exhibited particular modification styles in OSCC, which was independent of m.sup.6A-mRNA. Besides, m.sup.6A modification on circRNAs frequently occurred on the long exons in the front part of the coding sequence (CDS), which was distinct from m.sup.6A-mRNA that in 3'-UTR or stop codon. In conclusion, our work preliminarily demonstrates the traits of m.sup.6A-circRNAs, which may bring enlighten for the roles of m.sup.6A-circRNAs in OSCC.</description><subject>3' Untranslated regions</subject><subject>Cancer</subject><subject>Circular RNA</subject><subject>Diagnosis</subject><subject>Enzymes</subject><subject>Exons</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic transcription</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Immunoprecipitation</subject><subject>m6A-circRNAs</subject><subject>Medical prognosis</subject><subject>MeRIP-Seq</subject><subject>N6-Methyladenosine</subject><subject>Oral cancer</subject><subject>Oral carcinoma</subject><subject>Oral squamous cell carcinoma</subject><subject>Post-transcription</subject><subject>RNA</subject><subject>RNA modification</subject><subject>Squamous cell carcinoma</subject><subject>Stop 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m6A-modified circRNA in oral squamous cell carcinoma</atitle><jtitle>BMC genomics</jtitle><date>2022-08-23</date><risdate>2022</risdate><volume>23</volume><issue>1</issue><spage>1</spage><epage>611</epage><pages>1-611</pages><artnum>611</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>Emerging transcriptome-wide high-throughput screenings reveal the landscape and functions of RNAs, such as circular RNAs (circRNAs), in human cancer. In addition, the post-transcriptional RNA internal modifications, especially N.sup.6-methyladenosine (m.sup.6A), greatly enrich the variety of RNAs metabolism. However, the m.sup.6A modification on circRNAs has yet to be addressed. Here, we report an epitranscriptome-wide mapping of m.sup.6A-modified circRNAs (m.sup.6A-circRNA) in oral squamous cell carcinoma (OSCC). Utilizing the data of m.sup.6A methylated RNA immunoprecipitation sequencing (MeRIP-seq) and m.sup.6A-circRNAs microarray, we found that m.sup.6A-circRNAs exhibited particular modification styles in OSCC, which was independent of m.sup.6A-mRNA. Besides, m.sup.6A modification on circRNAs frequently occurred on the long exons in the front part of the coding sequence (CDS), which was distinct from m.sup.6A-mRNA that in 3'-UTR or stop codon. In conclusion, our work preliminarily demonstrates the traits of m.sup.6A-circRNAs, which may bring enlighten for the roles of m.sup.6A-circRNAs in OSCC.</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><pmid>35999496</pmid><doi>10.1186/s12864-022-08806-z</doi><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated regions Cancer Circular RNA Diagnosis Enzymes Exons Gene sequencing Genes Genetic aspects Genetic transcription Genomics Health aspects Immunoprecipitation m6A-circRNAs Medical prognosis MeRIP-Seq N6-Methyladenosine Oral cancer Oral carcinoma Oral squamous cell carcinoma Post-transcription RNA RNA modification Squamous cell carcinoma Stop codon Transcriptomes Tumorigenesis |
title | High-throughput microarray reveals the epitranscriptome-wide landscape of m6A-modified circRNA in oral squamous cell carcinoma |
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