Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis
Hemogen is a nuclear protein encoded by HEMGN (also known as hemogen in mouse, EDAG in human and RP59 in rat). It is considered to be a hematopoiesis‐specific gene that is expressed during the ontogeny of hematopoiesis. Herein, we characterize two distinct splicing variants of HEMGN mRNA with restri...
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Veröffentlicht in: | Developmental dynamics 2003-12, Vol.228 (4), p.606-616 |
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description | Hemogen is a nuclear protein encoded by HEMGN (also known as hemogen in mouse, EDAG in human and RP59 in rat). It is considered to be a hematopoiesis‐specific gene that is expressed during the ontogeny of hematopoiesis. Herein, we characterize two distinct splicing variants of HEMGN mRNA with restricted expression to hematopoietic cells and to round spermatids in the testis, respectively. Expression of the testis‐specific HEMGN mRNA (HEMGN‐t) is developmentally regulated and is concurrent with the first wave of meiosis in prepuberal mice. Sequence analysis reveals that HEMGN‐t and the hematopoietic HEMGN mRNA (HEMGN‐h) share a common coding sequence with distinct 5′ and 3′ untranslated regions and that these two isoforms are transcribed from the same gene locus, HEMGN, through the use of alternative promoters and polyadenylation sites. Thus, HEMGN expression exemplifies a developmental regulatory mechanism by which the diversification of gene expression is achieved through using distinct regulatory sequences in different cell types. Moreover, the existence of a testis‐specific isoform of HEMGN suggests a role in spermatogenesis. Finally, fluorescence in situ hybridization demonstrates that HEMGN is localized to chromosome 4 A5‐B2 in mouse and to chromosome 9q22 in human, which is a region known to harbor a cluster of leukemia breakpoints. Developmental Dynamics 228:606–616, 2003. © 2003 Wiley‐Liss, Inc. |
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It is considered to be a hematopoiesis‐specific gene that is expressed during the ontogeny of hematopoiesis. Herein, we characterize two distinct splicing variants of HEMGN mRNA with restricted expression to hematopoietic cells and to round spermatids in the testis, respectively. Expression of the testis‐specific HEMGN mRNA (HEMGN‐t) is developmentally regulated and is concurrent with the first wave of meiosis in prepuberal mice. Sequence analysis reveals that HEMGN‐t and the hematopoietic HEMGN mRNA (HEMGN‐h) share a common coding sequence with distinct 5′ and 3′ untranslated regions and that these two isoforms are transcribed from the same gene locus, HEMGN, through the use of alternative promoters and polyadenylation sites. Thus, HEMGN expression exemplifies a developmental regulatory mechanism by which the diversification of gene expression is achieved through using distinct regulatory sequences in different cell types. Moreover, the existence of a testis‐specific isoform of HEMGN suggests a role in spermatogenesis. Finally, fluorescence in situ hybridization demonstrates that HEMGN is localized to chromosome 4 A5‐B2 in mouse and to chromosome 9q22 in human, which is a region known to harbor a cluster of leukemia breakpoints. Developmental Dynamics 228:606–616, 2003. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/dvdy.10399</identifier><identifier>PMID: 14648837</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>3' Untranslated Regions ; 5' Untranslated Regions ; 9q22 ; Alternative Splicing ; Animals ; Base Sequence ; Blotting, Northern ; Blotting, Southern ; Bone Marrow - metabolism ; Cell Nucleus - metabolism ; Chromosome Mapping ; EDAG ; Female ; Gene Expression Regulation, Developmental ; Genome ; Hematopoiesis ; Hematopoietic Stem Cells - metabolism ; HEMGN ; Hemogen ; Humans ; In Situ Hybridization ; In Situ Hybridization, Fluorescence ; Male ; Meiosis ; Mice ; Models, Genetic ; Molecular Sequence Data ; Nuclear Proteins - biosynthesis ; Nuclear Proteins - chemistry ; Polyadenylation ; Promoter Regions, Genetic ; Protein Isoforms ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - metabolism ; RP59 ; Spermatids - metabolism ; Spermatogenesis ; testis ; Testis - metabolism</subject><ispartof>Developmental dynamics, 2003-12, Vol.228 (4), p.606-616</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3929-727d928df9d4927e0713585e89d03e92ef47977685ecebfb9d443225d6d4447d3</citedby><cites>FETCH-LOGICAL-c3929-727d928df9d4927e0713585e89d03e92ef47977685ecebfb9d443225d6d4447d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdvdy.10399$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdvdy.10399$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14648837$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Li V.</creatorcontrib><creatorcontrib>Heng, Henry H.</creatorcontrib><creatorcontrib>Wan, Junmei</creatorcontrib><creatorcontrib>Southwood, Cherie M.</creatorcontrib><creatorcontrib>Gow, Alexander</creatorcontrib><creatorcontrib>Li, Li</creatorcontrib><title>Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis</title><title>Developmental dynamics</title><addtitle>Dev Dyn</addtitle><description>Hemogen is a nuclear protein encoded by HEMGN (also known as hemogen in mouse, EDAG in human and RP59 in rat). It is considered to be a hematopoiesis‐specific gene that is expressed during the ontogeny of hematopoiesis. Herein, we characterize two distinct splicing variants of HEMGN mRNA with restricted expression to hematopoietic cells and to round spermatids in the testis, respectively. Expression of the testis‐specific HEMGN mRNA (HEMGN‐t) is developmentally regulated and is concurrent with the first wave of meiosis in prepuberal mice. Sequence analysis reveals that HEMGN‐t and the hematopoietic HEMGN mRNA (HEMGN‐h) share a common coding sequence with distinct 5′ and 3′ untranslated regions and that these two isoforms are transcribed from the same gene locus, HEMGN, through the use of alternative promoters and polyadenylation sites. Thus, HEMGN expression exemplifies a developmental regulatory mechanism by which the diversification of gene expression is achieved through using distinct regulatory sequences in different cell types. Moreover, the existence of a testis‐specific isoform of HEMGN suggests a role in spermatogenesis. Finally, fluorescence in situ hybridization demonstrates that HEMGN is localized to chromosome 4 A5‐B2 in mouse and to chromosome 9q22 in human, which is a region known to harbor a cluster of leukemia breakpoints. Developmental Dynamics 228:606–616, 2003. © 2003 Wiley‐Liss, Inc.</description><subject>3' Untranslated Regions</subject><subject>5' Untranslated Regions</subject><subject>9q22</subject><subject>Alternative Splicing</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Blotting, Northern</subject><subject>Blotting, Southern</subject><subject>Bone Marrow - metabolism</subject><subject>Cell Nucleus - metabolism</subject><subject>Chromosome Mapping</subject><subject>EDAG</subject><subject>Female</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genome</subject><subject>Hematopoiesis</subject><subject>Hematopoietic Stem Cells - metabolism</subject><subject>HEMGN</subject><subject>Hemogen</subject><subject>Humans</subject><subject>In Situ Hybridization</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Meiosis</subject><subject>Mice</subject><subject>Models, Genetic</subject><subject>Molecular Sequence Data</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>Nuclear Proteins - chemistry</subject><subject>Polyadenylation</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Isoforms</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - metabolism</subject><subject>RP59</subject><subject>Spermatids - metabolism</subject><subject>Spermatogenesis</subject><subject>testis</subject><subject>Testis - metabolism</subject><issn>1058-8388</issn><issn>1097-0177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1O3TAQhS1UVCh0wwNUXnVRKa3_EttLBC1UQmIDSKyi3Hhy6yqJU09Cm10fgAXP2CepQ67Erl3NmeNPZ2QdQk44-8gZE5_cg5uTktbukUPOrM4Y1_rVonOTGWnMAXmD-J0xZgrFX5MDrgpljNSH5PG0HSH21egfgA4xdCGtSKve0SG0c-Wgn9v0GnoaYTslCXT0iBP8-f2EA9S-8TWFX0MExIUKDb2ELmyhpx5DE2KH1E3R91v6DbpqDEPwgH49kQLi4iV68Y7JflO1CG9384jcfvl8c3aZXV1ffD07vcpqaYXNtNDOCuMa65QVGpjmMjc5GOuYBCugUdpqXSSrhk2zSZiSQuSuSEJpJ4_I-zU3ffjHBDiWncca2rbqIUxYaq5Eni79FxRMGq7yIoEfVrCOATFCUw7Rd1WcS87KpaRyKal8LinB73ap06YD94LuWkkAX4GfvoX5H1Hl-d35_Rr6F467oh8</recordid><startdate>200312</startdate><enddate>200312</enddate><creator>Yang, Li V.</creator><creator>Heng, Henry H.</creator><creator>Wan, Junmei</creator><creator>Southwood, Cherie M.</creator><creator>Gow, Alexander</creator><creator>Li, Li</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200312</creationdate><title>Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis</title><author>Yang, Li V. ; Heng, Henry H. ; Wan, Junmei ; Southwood, Cherie M. ; Gow, Alexander ; Li, Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3929-727d928df9d4927e0713585e89d03e92ef47977685ecebfb9d443225d6d4447d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>3' Untranslated Regions</topic><topic>5' Untranslated Regions</topic><topic>9q22</topic><topic>Alternative Splicing</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Blotting, Northern</topic><topic>Blotting, Southern</topic><topic>Bone Marrow - metabolism</topic><topic>Cell Nucleus - metabolism</topic><topic>Chromosome Mapping</topic><topic>EDAG</topic><topic>Female</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genome</topic><topic>Hematopoiesis</topic><topic>Hematopoietic Stem Cells - metabolism</topic><topic>HEMGN</topic><topic>Hemogen</topic><topic>Humans</topic><topic>In Situ Hybridization</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Meiosis</topic><topic>Mice</topic><topic>Models, Genetic</topic><topic>Molecular Sequence Data</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>Nuclear Proteins - chemistry</topic><topic>Polyadenylation</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Isoforms</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - metabolism</topic><topic>RP59</topic><topic>Spermatids - metabolism</topic><topic>Spermatogenesis</topic><topic>testis</topic><topic>Testis - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Li V.</creatorcontrib><creatorcontrib>Heng, Henry H.</creatorcontrib><creatorcontrib>Wan, Junmei</creatorcontrib><creatorcontrib>Southwood, Cherie M.</creatorcontrib><creatorcontrib>Gow, Alexander</creatorcontrib><creatorcontrib>Li, Li</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Li V.</au><au>Heng, Henry H.</au><au>Wan, Junmei</au><au>Southwood, Cherie M.</au><au>Gow, Alexander</au><au>Li, Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>2003-12</date><risdate>2003</risdate><volume>228</volume><issue>4</issue><spage>606</spage><epage>616</epage><pages>606-616</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><abstract>Hemogen is a nuclear protein encoded by HEMGN (also known as hemogen in mouse, EDAG in human and RP59 in rat). It is considered to be a hematopoiesis‐specific gene that is expressed during the ontogeny of hematopoiesis. Herein, we characterize two distinct splicing variants of HEMGN mRNA with restricted expression to hematopoietic cells and to round spermatids in the testis, respectively. Expression of the testis‐specific HEMGN mRNA (HEMGN‐t) is developmentally regulated and is concurrent with the first wave of meiosis in prepuberal mice. Sequence analysis reveals that HEMGN‐t and the hematopoietic HEMGN mRNA (HEMGN‐h) share a common coding sequence with distinct 5′ and 3′ untranslated regions and that these two isoforms are transcribed from the same gene locus, HEMGN, through the use of alternative promoters and polyadenylation sites. Thus, HEMGN expression exemplifies a developmental regulatory mechanism by which the diversification of gene expression is achieved through using distinct regulatory sequences in different cell types. Moreover, the existence of a testis‐specific isoform of HEMGN suggests a role in spermatogenesis. Finally, fluorescence in situ hybridization demonstrates that HEMGN is localized to chromosome 4 A5‐B2 in mouse and to chromosome 9q22 in human, which is a region known to harbor a cluster of leukemia breakpoints. Developmental Dynamics 228:606–616, 2003. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14648837</pmid><doi>10.1002/dvdy.10399</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated Regions 5' Untranslated Regions 9q22 Alternative Splicing Animals Base Sequence Blotting, Northern Blotting, Southern Bone Marrow - metabolism Cell Nucleus - metabolism Chromosome Mapping EDAG Female Gene Expression Regulation, Developmental Genome Hematopoiesis Hematopoietic Stem Cells - metabolism HEMGN Hemogen Humans In Situ Hybridization In Situ Hybridization, Fluorescence Male Meiosis Mice Models, Genetic Molecular Sequence Data Nuclear Proteins - biosynthesis Nuclear Proteins - chemistry Polyadenylation Promoter Regions, Genetic Protein Isoforms Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - metabolism RP59 Spermatids - metabolism Spermatogenesis testis Testis - metabolism |
title | Alternative promoters and polyadenylation regulate tissue‐specific expression of Hemogen isoforms during hematopoiesis and spermatogenesis |
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