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Novel circular RNAs of the apoptosis‐related BAX and BCL2L12 genes identified in a chronic lymphocytic leukemia cell line using nanopore sequencing
Circular RNAs (circRNAs), a novel RNA type generated by back‐splicing, are key regulators of gene expression, with deregulated expression and established involvement in leukemia. The products of BCL2 and its homologs, including BAX and BCL2L12, are implicated in chronic lymphocytic leukemia (CLL). H...
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Published in: | FEBS open bio 2023-10, Vol.13 (10), p.1953-1966 |
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creator | Kontos, Christos K. Karousi, Paraskevi Artemaki, Pinelopi I. Abdelgawad, Ahmed Dimitriadou, Aspasia Machairas, Nikolaos P. Sideris, Diamantis C. Pappa, Vasiliki Scorilas, Andreas Batish, Mona Papageorgiou, Sotirios G. |
description | Circular RNAs (circRNAs), a novel RNA type generated by back‐splicing, are key regulators of gene expression, with deregulated expression and established involvement in leukemia. The products of BCL2 and its homologs, including BAX and BCL2L12, are implicated in chronic lymphocytic leukemia (CLL). However, to the best of our knowledge, nothing is known about circRNAs produced by these two genes and their role in CLL. We sought to further elucidate the contribution of BAX and BCL2L12 in CLL by unraveling the identity, localization, and potential role of their circRNAs. Therefore, total RNA from the EHEB cell line and peripheral blood mononuclear cells (PBMCs) of CLL patients and non‐leukemic blood donors was extracted and reverse‐transcribed using random hexamers. Next, nested PCRs with divergent primers were performed and the purified PCR products were subjected to 3rd generation nanopore sequencing. Nested PCRs were also applied to first‐strand cDNAs synthesized from total RNA extracts of PBMCs from CLL patients and non‐leukemic blood donors. Lastly, a single‐molecule resolution fluorescent in situ hybridization method called circFISH was used to visualize the circRNA distribution in EHEB cells. We discovered several novel circRNAs produced by BAX and BCL2L12, which were characterized by great exon structure diversity. In addition, intriguing findings regarding their formation emerged. Interestingly, visualization of the most abundant circRNAs showed distinct intracellular localization. Moreover, a complex BAX and BCL2L12 circRNA expression pattern was revealed in CLL patients and non‐leukemic blood donors. Our data suggest a multifaceted role of BAX and BCL2L12 circRNAs in B‐cell CLL.
Novel circular RNAs (circRNAs) deriving from BAX and BCL2L12 were discovered using nanopore sequencing. These circRNAs exhibit diverse exon structures, distinct intracellular localization, and may interact with microRNAs with a proven role in chronic lymphocytic leukemia (CLL). A complex circRNA expression pattern in CLL patients and non‐leukemic blood donors was found as well. Our findings suggest a multifaceted role of these circRNAs in B‐cell CLL. |
doi_str_mv | 10.1002/2211-5463.13672 |
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Novel circular RNAs (circRNAs) deriving from BAX and BCL2L12 were discovered using nanopore sequencing. These circRNAs exhibit diverse exon structures, distinct intracellular localization, and may interact with microRNAs with a proven role in chronic lymphocytic leukemia (CLL). A complex circRNA expression pattern in CLL patients and non‐leukemic blood donors was found as well. Our findings suggest a multifaceted role of these circRNAs in B‐cell CLL.</description><identifier>ISSN: 2211-5463</identifier><identifier>EISSN: 2211-5463</identifier><identifier>DOI: 10.1002/2211-5463.13672</identifier><identifier>PMID: 37424436</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Apoptosis ; BAX protein ; Bcl-2 protein ; BCL2 family ; Biomarkers ; Blood & organ donations ; Blood donors ; Chronic lymphocytic leukemia ; circRNA ; Circular RNA ; DNA polymerase ; Fluorescence in situ hybridization ; Gene expression ; Genes ; Hematological Cancer ; Hexamers ; Investigations ; Leukemia ; Leukocytes (mononuclear) ; Localization ; Lymphocytes B ; MicroRNAs ; Non-Coding RNA ; Pathogenesis ; Peripheral blood mononuclear cells ; Polymerase chain reaction ; pro‐apoptotic ; Ribonucleic acid ; RNA ; RNA Sequencing ; single‐molecule fluorescence in situ hybridization ; third generation (long‐read) sequencing ; transcriptomics</subject><ispartof>FEBS open bio, 2023-10, Vol.13 (10), p.1953-1966</ispartof><rights>2023 The Authors. published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.</rights><rights>This article is protected by copyright. All rights reserved.</rights><rights>2023. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4892-395e4f091b901d26ff08d4f1257c935744758507675c7b73ee9f673011fb423</cites><orcidid>0000-0001-9039-6149 ; 0009-0008-9682-1036 ; 0000-0002-8175-639X ; 0009-0004-6398-8156 ; 0000-0002-9935-8461 ; 0000-0003-2427-4949 ; 0000-0001-8435-4428 ; 0000-0003-0421-9424 ; 0000-0001-5002-0390 ; 0000-0001-6518-0098 ; 0000-0002-3376-837X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2872171137/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2872171137?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37424436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kontos, Christos K.</creatorcontrib><creatorcontrib>Karousi, Paraskevi</creatorcontrib><creatorcontrib>Artemaki, Pinelopi I.</creatorcontrib><creatorcontrib>Abdelgawad, Ahmed</creatorcontrib><creatorcontrib>Dimitriadou, Aspasia</creatorcontrib><creatorcontrib>Machairas, Nikolaos P.</creatorcontrib><creatorcontrib>Sideris, Diamantis C.</creatorcontrib><creatorcontrib>Pappa, Vasiliki</creatorcontrib><creatorcontrib>Scorilas, Andreas</creatorcontrib><creatorcontrib>Batish, Mona</creatorcontrib><creatorcontrib>Papageorgiou, Sotirios G.</creatorcontrib><title>Novel circular RNAs of the apoptosis‐related BAX and BCL2L12 genes identified in a chronic lymphocytic leukemia cell line using nanopore sequencing</title><title>FEBS open bio</title><addtitle>FEBS Open Bio</addtitle><description>Circular RNAs (circRNAs), a novel RNA type generated by back‐splicing, are key regulators of gene expression, with deregulated expression and established involvement in leukemia. The products of BCL2 and its homologs, including BAX and BCL2L12, are implicated in chronic lymphocytic leukemia (CLL). However, to the best of our knowledge, nothing is known about circRNAs produced by these two genes and their role in CLL. We sought to further elucidate the contribution of BAX and BCL2L12 in CLL by unraveling the identity, localization, and potential role of their circRNAs. Therefore, total RNA from the EHEB cell line and peripheral blood mononuclear cells (PBMCs) of CLL patients and non‐leukemic blood donors was extracted and reverse‐transcribed using random hexamers. Next, nested PCRs with divergent primers were performed and the purified PCR products were subjected to 3rd generation nanopore sequencing. Nested PCRs were also applied to first‐strand cDNAs synthesized from total RNA extracts of PBMCs from CLL patients and non‐leukemic blood donors. Lastly, a single‐molecule resolution fluorescent in situ hybridization method called circFISH was used to visualize the circRNA distribution in EHEB cells. We discovered several novel circRNAs produced by BAX and BCL2L12, which were characterized by great exon structure diversity. In addition, intriguing findings regarding their formation emerged. Interestingly, visualization of the most abundant circRNAs showed distinct intracellular localization. Moreover, a complex BAX and BCL2L12 circRNA expression pattern was revealed in CLL patients and non‐leukemic blood donors. Our data suggest a multifaceted role of BAX and BCL2L12 circRNAs in B‐cell CLL.
Novel circular RNAs (circRNAs) deriving from BAX and BCL2L12 were discovered using nanopore sequencing. These circRNAs exhibit diverse exon structures, distinct intracellular localization, and may interact with microRNAs with a proven role in chronic lymphocytic leukemia (CLL). A complex circRNA expression pattern in CLL patients and non‐leukemic blood donors was found as well. Our findings suggest a multifaceted role of these circRNAs in B‐cell CLL.</description><subject>Apoptosis</subject><subject>BAX protein</subject><subject>Bcl-2 protein</subject><subject>BCL2 family</subject><subject>Biomarkers</subject><subject>Blood & organ donations</subject><subject>Blood donors</subject><subject>Chronic lymphocytic leukemia</subject><subject>circRNA</subject><subject>Circular RNA</subject><subject>DNA polymerase</subject><subject>Fluorescence in situ hybridization</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Hematological Cancer</subject><subject>Hexamers</subject><subject>Investigations</subject><subject>Leukemia</subject><subject>Leukocytes (mononuclear)</subject><subject>Localization</subject><subject>Lymphocytes B</subject><subject>MicroRNAs</subject><subject>Non-Coding RNA</subject><subject>Pathogenesis</subject><subject>Peripheral blood mononuclear cells</subject><subject>Polymerase chain reaction</subject><subject>pro‐apoptotic</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA Sequencing</subject><subject>single‐molecule fluorescence in situ hybridization</subject><subject>third generation (long‐read) sequencing</subject><subject>transcriptomics</subject><issn>2211-5463</issn><issn>2211-5463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFks9u1DAQxiMEotXSMzdkiQuXbf03jk-oXbVQaVUk4MDNcpzJrpesHeykaG88AhdekCfB6ZZVywVfZjTz-afx-CuKlwSfEozpGaWEzAUv2SlhpaRPiuND5emD_Kg4SWmD8ykxKTF-XhwxySnnrDwuft2EW-iQddGOnYno4815QqFFwxqQ6UM_hOTS7x8_I3RmgAZdnH9Bxue4WNIloWgFHhJyDfjBtS4LnEcG2XUM3lnU7bb9OtjdMOUwfoWty03oOtQ5D2hMzq-QNz70IQJK8G0Eb3PtRfGsNV2Ck_s4Kz5dXX5evJ8vP7y7Xpwv55ZXis6ZEsBbrEitMGlo2ba4anhLqJBWMSE5l6ISWJZSWFlLBqDaUjJMSFtzymbF9Z7aBLPRfXRbE3c6GKfvCiGutIl59A40q0ytFGukUpQLBZVoJJRt1di6sTajZ8XbPasf6y00Nu8jmu4R9HHHu7VehVtNsOCKEpUJb-4JMeQ9pEFvXZp2ZTyEMWlaifxlRIgqS1__I92EMfq8qaySlEhC2DTS2V5lY0gpQnuYhmA9GUhPFtGTRfSdgfKNVw8fcdD_tUsWlHvBd9fB7n88fXV5wffkP4tQ0Ho</recordid><startdate>202310</startdate><enddate>202310</enddate><creator>Kontos, Christos K.</creator><creator>Karousi, Paraskevi</creator><creator>Artemaki, Pinelopi I.</creator><creator>Abdelgawad, Ahmed</creator><creator>Dimitriadou, Aspasia</creator><creator>Machairas, Nikolaos P.</creator><creator>Sideris, Diamantis C.</creator><creator>Pappa, Vasiliki</creator><creator>Scorilas, Andreas</creator><creator>Batish, Mona</creator><creator>Papageorgiou, Sotirios G.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9039-6149</orcidid><orcidid>https://orcid.org/0009-0008-9682-1036</orcidid><orcidid>https://orcid.org/0000-0002-8175-639X</orcidid><orcidid>https://orcid.org/0009-0004-6398-8156</orcidid><orcidid>https://orcid.org/0000-0002-9935-8461</orcidid><orcidid>https://orcid.org/0000-0003-2427-4949</orcidid><orcidid>https://orcid.org/0000-0001-8435-4428</orcidid><orcidid>https://orcid.org/0000-0003-0421-9424</orcidid><orcidid>https://orcid.org/0000-0001-5002-0390</orcidid><orcidid>https://orcid.org/0000-0001-6518-0098</orcidid><orcidid>https://orcid.org/0000-0002-3376-837X</orcidid></search><sort><creationdate>202310</creationdate><title>Novel circular RNAs of the apoptosis‐related BAX and BCL2L12 genes identified in a chronic lymphocytic leukemia cell line using nanopore sequencing</title><author>Kontos, Christos K. ; Karousi, Paraskevi ; Artemaki, Pinelopi I. ; Abdelgawad, Ahmed ; Dimitriadou, Aspasia ; Machairas, Nikolaos P. ; Sideris, Diamantis C. ; Pappa, Vasiliki ; Scorilas, Andreas ; Batish, Mona ; Papageorgiou, Sotirios G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4892-395e4f091b901d26ff08d4f1257c935744758507675c7b73ee9f673011fb423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Apoptosis</topic><topic>BAX protein</topic><topic>Bcl-2 protein</topic><topic>BCL2 family</topic><topic>Biomarkers</topic><topic>Blood & organ donations</topic><topic>Blood donors</topic><topic>Chronic lymphocytic leukemia</topic><topic>circRNA</topic><topic>Circular RNA</topic><topic>DNA polymerase</topic><topic>Fluorescence in situ hybridization</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Hematological Cancer</topic><topic>Hexamers</topic><topic>Investigations</topic><topic>Leukemia</topic><topic>Leukocytes (mononuclear)</topic><topic>Localization</topic><topic>Lymphocytes B</topic><topic>MicroRNAs</topic><topic>Non-Coding RNA</topic><topic>Pathogenesis</topic><topic>Peripheral blood mononuclear cells</topic><topic>Polymerase chain reaction</topic><topic>pro‐apoptotic</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA Sequencing</topic><topic>single‐molecule fluorescence in situ hybridization</topic><topic>third generation (long‐read) sequencing</topic><topic>transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kontos, Christos K.</creatorcontrib><creatorcontrib>Karousi, Paraskevi</creatorcontrib><creatorcontrib>Artemaki, Pinelopi I.</creatorcontrib><creatorcontrib>Abdelgawad, Ahmed</creatorcontrib><creatorcontrib>Dimitriadou, Aspasia</creatorcontrib><creatorcontrib>Machairas, Nikolaos P.</creatorcontrib><creatorcontrib>Sideris, Diamantis C.</creatorcontrib><creatorcontrib>Pappa, Vasiliki</creatorcontrib><creatorcontrib>Scorilas, Andreas</creatorcontrib><creatorcontrib>Batish, Mona</creatorcontrib><creatorcontrib>Papageorgiou, Sotirios G.</creatorcontrib><collection>Open Access: Wiley-Blackwell Open Access Journals</collection><collection>Wiley Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>FEBS open bio</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kontos, Christos K.</au><au>Karousi, Paraskevi</au><au>Artemaki, Pinelopi I.</au><au>Abdelgawad, Ahmed</au><au>Dimitriadou, Aspasia</au><au>Machairas, Nikolaos P.</au><au>Sideris, Diamantis C.</au><au>Pappa, Vasiliki</au><au>Scorilas, Andreas</au><au>Batish, Mona</au><au>Papageorgiou, Sotirios G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel circular RNAs of the apoptosis‐related BAX and BCL2L12 genes identified in a chronic lymphocytic leukemia cell line using nanopore sequencing</atitle><jtitle>FEBS open bio</jtitle><addtitle>FEBS Open Bio</addtitle><date>2023-10</date><risdate>2023</risdate><volume>13</volume><issue>10</issue><spage>1953</spage><epage>1966</epage><pages>1953-1966</pages><issn>2211-5463</issn><eissn>2211-5463</eissn><abstract>Circular RNAs (circRNAs), a novel RNA type generated by back‐splicing, are key regulators of gene expression, with deregulated expression and established involvement in leukemia. The products of BCL2 and its homologs, including BAX and BCL2L12, are implicated in chronic lymphocytic leukemia (CLL). However, to the best of our knowledge, nothing is known about circRNAs produced by these two genes and their role in CLL. We sought to further elucidate the contribution of BAX and BCL2L12 in CLL by unraveling the identity, localization, and potential role of their circRNAs. Therefore, total RNA from the EHEB cell line and peripheral blood mononuclear cells (PBMCs) of CLL patients and non‐leukemic blood donors was extracted and reverse‐transcribed using random hexamers. Next, nested PCRs with divergent primers were performed and the purified PCR products were subjected to 3rd generation nanopore sequencing. Nested PCRs were also applied to first‐strand cDNAs synthesized from total RNA extracts of PBMCs from CLL patients and non‐leukemic blood donors. Lastly, a single‐molecule resolution fluorescent in situ hybridization method called circFISH was used to visualize the circRNA distribution in EHEB cells. We discovered several novel circRNAs produced by BAX and BCL2L12, which were characterized by great exon structure diversity. In addition, intriguing findings regarding their formation emerged. Interestingly, visualization of the most abundant circRNAs showed distinct intracellular localization. Moreover, a complex BAX and BCL2L12 circRNA expression pattern was revealed in CLL patients and non‐leukemic blood donors. Our data suggest a multifaceted role of BAX and BCL2L12 circRNAs in B‐cell CLL.
Novel circular RNAs (circRNAs) deriving from BAX and BCL2L12 were discovered using nanopore sequencing. These circRNAs exhibit diverse exon structures, distinct intracellular localization, and may interact with microRNAs with a proven role in chronic lymphocytic leukemia (CLL). A complex circRNA expression pattern in CLL patients and non‐leukemic blood donors was found as well. Our findings suggest a multifaceted role of these circRNAs in B‐cell CLL.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>37424436</pmid><doi>10.1002/2211-5463.13672</doi><tpages>1966</tpages><orcidid>https://orcid.org/0000-0001-9039-6149</orcidid><orcidid>https://orcid.org/0009-0008-9682-1036</orcidid><orcidid>https://orcid.org/0000-0002-8175-639X</orcidid><orcidid>https://orcid.org/0009-0004-6398-8156</orcidid><orcidid>https://orcid.org/0000-0002-9935-8461</orcidid><orcidid>https://orcid.org/0000-0003-2427-4949</orcidid><orcidid>https://orcid.org/0000-0001-8435-4428</orcidid><orcidid>https://orcid.org/0000-0003-0421-9424</orcidid><orcidid>https://orcid.org/0000-0001-5002-0390</orcidid><orcidid>https://orcid.org/0000-0001-6518-0098</orcidid><orcidid>https://orcid.org/0000-0002-3376-837X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis BAX protein Bcl-2 protein BCL2 family Biomarkers Blood & organ donations Blood donors Chronic lymphocytic leukemia circRNA Circular RNA DNA polymerase Fluorescence in situ hybridization Gene expression Genes Hematological Cancer Hexamers Investigations Leukemia Leukocytes (mononuclear) Localization Lymphocytes B MicroRNAs Non-Coding RNA Pathogenesis Peripheral blood mononuclear cells Polymerase chain reaction pro‐apoptotic Ribonucleic acid RNA RNA Sequencing single‐molecule fluorescence in situ hybridization third generation (long‐read) sequencing transcriptomics |
title | Novel circular RNAs of the apoptosis‐related BAX and BCL2L12 genes identified in a chronic lymphocytic leukemia cell line using nanopore sequencing |
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