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Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell
Marek's disease (MD), a highly contagious T cell lymphoid neoplasia disease of chickens, causes huge economic losses to the poultry industry. It is the only one tumor disease which can be prevented by vaccine in chickens; therefore, MD is considered to be an excellent model to study the pathoge...
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Published in: | In vitro cellular & developmental biology. Animal 2021-03, Vol.57 (3), p.272-279 |
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description | Marek's disease (MD), a highly contagious T cell lymphoid neoplasia disease of chickens, causes huge economic losses to the poultry industry. It is the only one tumor disease which can be prevented by vaccine in chickens; therefore, MD is considered to be an excellent model to study the pathogenesis of virus-induced cancer. Recently, abundant evidences have verified that miRNAs are regulators in the process of neoplastic transformation. In our previous study on miRNome analysis of MDV-induced lymphoma in chicken, we found that gga-miR-181a was downregulated drastically in MDV-infected spleens. To further investigate the role of gga-miR-181a in MDV-induced lymphomagenesis, we performed cell migration assay, and the results suggested that gga-miR-181a suppressed the migration of MDV-transformed lymphoid cell (MSB-1). Subsequently, luciferase reporter gene assay revealed that acidic nuclear phosphoprotein 32A (ANP32A) was a functional target gene of gga-miR181a. Real-time PCR and western blot assay showed that the mRNA and protein levels of ANP32A were downregulated in gga-miR181a mimic group at 48-h and 96-h post-transfection, respectively, indicating that ANP32A was modulated by gga-miR- 181a. All the results suggested that gga-miR-181a was an inhibitor in MSB-1 cell migration. ANP32A was a direct target gene of gga-miR-181a and they were implicated in MD lymphoma tumorigenesis. |
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It is the only one tumor disease which can be prevented by vaccine in chickens; therefore, MD is considered to be an excellent model to study the pathogenesis of virus-induced cancer. Recently, abundant evidences have verified that miRNAs are regulators in the process of neoplastic transformation. In our previous study on miRNome analysis of MDV-induced lymphoma in chicken, we found that gga-miR-181a was downregulated drastically in MDV-infected spleens. To further investigate the role of gga-miR-181a in MDV-induced lymphomagenesis, we performed cell migration assay, and the results suggested that gga-miR-181a suppressed the migration of MDV-transformed lymphoid cell (MSB-1). Subsequently, luciferase reporter gene assay revealed that acidic nuclear phosphoprotein 32A (ANP32A) was a functional target gene of gga-miR181a. Real-time PCR and western blot assay showed that the mRNA and protein levels of ANP32A were downregulated in gga-miR181a mimic group at 48-h and 96-h post-transfection, respectively, indicating that ANP32A was modulated by gga-miR- 181a. All the results suggested that gga-miR-181a was an inhibitor in MSB-1 cell migration. ANP32A was a direct target gene of gga-miR-181a and they were implicated in MD lymphoma tumorigenesis.</description><identifier>ISSN: 1071-2690</identifier><identifier>EISSN: 1543-706X</identifier><identifier>DOI: 10.1007/s11626-021-00550-0</identifier><identifier>PMID: 33686586</identifier><language>eng</language><publisher>New York: Springer Science & Business Media LLC</publisher><subject>Animal Genetics and Genomics ; Assaying ; Biomedical and Life Sciences ; Cell adhesion & migration ; Cell Biology ; Cell Culture ; CELL GROWTH/DIFFERENTIATION/APOPTOSIS ; Cell migration ; Chickens ; Developmental Biology ; Economic impact ; Life Sciences ; Lymphocytes ; Lymphocytes T ; Lymphoma ; Marek's disease ; mRNA ; Pathogenesis ; Regulators ; Reporter gene ; Stem Cells ; Transfection ; Tumorigenesis ; Vaccines ; Viruses</subject><ispartof>In vitro cellular & developmental biology. Animal, 2021-03, Vol.57 (3), p.272-279</ispartof><rights>2021 Society for In Vitro Biology</rights><rights>The Society for In Vitro Biology 2021</rights><rights>The Society for In Vitro Biology 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-72b9675dd7de8ca93dad550514d08dcbadccb970b33b5d0f2cb302685c8579953</citedby><cites>FETCH-LOGICAL-c405t-72b9675dd7de8ca93dad550514d08dcbadccb970b33b5d0f2cb302685c8579953</cites><orcidid>0000-0001-8234-5827</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33686586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, X.</creatorcontrib><creatorcontrib>Zhao, C.</creatorcontrib><creatorcontrib>Han, B.</creatorcontrib><creatorcontrib>Qu, L.</creatorcontrib><creatorcontrib>Liu, C.</creatorcontrib><creatorcontrib>Yang, N.</creatorcontrib><creatorcontrib>Lian, L.</creatorcontrib><title>Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell</title><title>In vitro cellular & developmental biology. Animal</title><addtitle>In Vitro Cell.Dev.Biol.-Animal</addtitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><description>Marek's disease (MD), a highly contagious T cell lymphoid neoplasia disease of chickens, causes huge economic losses to the poultry industry. It is the only one tumor disease which can be prevented by vaccine in chickens; therefore, MD is considered to be an excellent model to study the pathogenesis of virus-induced cancer. Recently, abundant evidences have verified that miRNAs are regulators in the process of neoplastic transformation. In our previous study on miRNome analysis of MDV-induced lymphoma in chicken, we found that gga-miR-181a was downregulated drastically in MDV-infected spleens. To further investigate the role of gga-miR-181a in MDV-induced lymphomagenesis, we performed cell migration assay, and the results suggested that gga-miR-181a suppressed the migration of MDV-transformed lymphoid cell (MSB-1). Subsequently, luciferase reporter gene assay revealed that acidic nuclear phosphoprotein 32A (ANP32A) was a functional target gene of gga-miR181a. Real-time PCR and western blot assay showed that the mRNA and protein levels of ANP32A were downregulated in gga-miR181a mimic group at 48-h and 96-h post-transfection, respectively, indicating that ANP32A was modulated by gga-miR- 181a. All the results suggested that gga-miR-181a was an inhibitor in MSB-1 cell migration. ANP32A was a direct target gene of gga-miR-181a and they were implicated in MD lymphoma tumorigenesis.</description><subject>Animal Genetics and Genomics</subject><subject>Assaying</subject><subject>Biomedical and Life Sciences</subject><subject>Cell adhesion & migration</subject><subject>Cell Biology</subject><subject>Cell Culture</subject><subject>CELL GROWTH/DIFFERENTIATION/APOPTOSIS</subject><subject>Cell migration</subject><subject>Chickens</subject><subject>Developmental Biology</subject><subject>Economic impact</subject><subject>Life Sciences</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Lymphoma</subject><subject>Marek's disease</subject><subject>mRNA</subject><subject>Pathogenesis</subject><subject>Regulators</subject><subject>Reporter gene</subject><subject>Stem Cells</subject><subject>Transfection</subject><subject>Tumorigenesis</subject><subject>Vaccines</subject><subject>Viruses</subject><issn>1071-2690</issn><issn>1543-706X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kF1LHDEUhoNY_Nj2D3ghAyJ4Ez1JJl-X63argtrSD_AuZJKszrIzsyYz0P77xs5axQtzk0Ce95yXB6EDAqcEQJ4lQgQVGCjBAJwDhi20R3jJsARxt53fIAmmQsMu2k9pCfloInbQLmNCCa7EHppf3Fvc1N8xUcQWTeeHle1DKqa33xidFuH3OoaU6q4tbOuLun2oq7pPxc3n2Qzf_DjHpHBhtfqIPizsKoVPm3uCfn2Z_5xd4uuvF1ez6TV2JfAeS1ppIbn30gflrGbe-tybk9KD8q6y3rlKS6gYq7iHBXUVAyoUd4pLrTmboJNx7jp2j0NIvWnq9FTAtqEbkqGl1kypksmMHr1Bl90Q29zOUA5C0DLLyxQdKRe7lGJYmHWsGxv_GALmSbIZJZss2fyTbCCHDjejh6oJ_n_k2WoG2Aik_NXeh_iy-92xx2Nqmfouvi5CWU6UnKm8QbO_mNeO0A</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Li, X.</creator><creator>Zhao, C.</creator><creator>Han, B.</creator><creator>Qu, L.</creator><creator>Liu, C.</creator><creator>Yang, N.</creator><creator>Lian, L.</creator><general>Springer Science & Business Media LLC</general><general>Springer US</general><general>Society for In Vitro Biology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8234-5827</orcidid></search><sort><creationdate>20210301</creationdate><title>Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell</title><author>Li, X. ; Zhao, C. ; Han, B. ; Qu, L. ; Liu, C. ; Yang, N. ; Lian, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-72b9675dd7de8ca93dad550514d08dcbadccb970b33b5d0f2cb302685c8579953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animal Genetics and Genomics</topic><topic>Assaying</topic><topic>Biomedical and Life Sciences</topic><topic>Cell adhesion & migration</topic><topic>Cell Biology</topic><topic>Cell Culture</topic><topic>CELL GROWTH/DIFFERENTIATION/APOPTOSIS</topic><topic>Cell migration</topic><topic>Chickens</topic><topic>Developmental Biology</topic><topic>Economic impact</topic><topic>Life Sciences</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Lymphoma</topic><topic>Marek's disease</topic><topic>mRNA</topic><topic>Pathogenesis</topic><topic>Regulators</topic><topic>Reporter gene</topic><topic>Stem Cells</topic><topic>Transfection</topic><topic>Tumorigenesis</topic><topic>Vaccines</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, X.</creatorcontrib><creatorcontrib>Zhao, C.</creatorcontrib><creatorcontrib>Han, B.</creatorcontrib><creatorcontrib>Qu, L.</creatorcontrib><creatorcontrib>Liu, C.</creatorcontrib><creatorcontrib>Yang, N.</creatorcontrib><creatorcontrib>Lian, L.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>In vitro cellular & developmental biology. Animal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, X.</au><au>Zhao, C.</au><au>Han, B.</au><au>Qu, L.</au><au>Liu, C.</au><au>Yang, N.</au><au>Lian, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell</atitle><jtitle>In vitro cellular & developmental biology. Animal</jtitle><stitle>In Vitro Cell.Dev.Biol.-Animal</stitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>57</volume><issue>3</issue><spage>272</spage><epage>279</epage><pages>272-279</pages><issn>1071-2690</issn><eissn>1543-706X</eissn><abstract>Marek's disease (MD), a highly contagious T cell lymphoid neoplasia disease of chickens, causes huge economic losses to the poultry industry. It is the only one tumor disease which can be prevented by vaccine in chickens; therefore, MD is considered to be an excellent model to study the pathogenesis of virus-induced cancer. Recently, abundant evidences have verified that miRNAs are regulators in the process of neoplastic transformation. In our previous study on miRNome analysis of MDV-induced lymphoma in chicken, we found that gga-miR-181a was downregulated drastically in MDV-infected spleens. To further investigate the role of gga-miR-181a in MDV-induced lymphomagenesis, we performed cell migration assay, and the results suggested that gga-miR-181a suppressed the migration of MDV-transformed lymphoid cell (MSB-1). Subsequently, luciferase reporter gene assay revealed that acidic nuclear phosphoprotein 32A (ANP32A) was a functional target gene of gga-miR181a. Real-time PCR and western blot assay showed that the mRNA and protein levels of ANP32A were downregulated in gga-miR181a mimic group at 48-h and 96-h post-transfection, respectively, indicating that ANP32A was modulated by gga-miR- 181a. All the results suggested that gga-miR-181a was an inhibitor in MSB-1 cell migration. ANP32A was a direct target gene of gga-miR-181a and they were implicated in MD lymphoma tumorigenesis.</abstract><cop>New York</cop><pub>Springer Science & Business Media LLC</pub><pmid>33686586</pmid><doi>10.1007/s11626-021-00550-0</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8234-5827</orcidid></addata></record> |
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subjects | Animal Genetics and Genomics Assaying Biomedical and Life Sciences Cell adhesion & migration Cell Biology Cell Culture CELL GROWTH/DIFFERENTIATION/APOPTOSIS Cell migration Chickens Developmental Biology Economic impact Life Sciences Lymphocytes Lymphocytes T Lymphoma Marek's disease mRNA Pathogenesis Regulators Reporter gene Stem Cells Transfection Tumorigenesis Vaccines Viruses |
title | Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell |
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