Expression of estrogen receptor alpha exon-deleted mRNA variants in the human and non-human primate frontal cortex
Although estrogen receptor alpha (ERα) mRNA has been detected in the primate frontal cortex, the types of ERα transcripts expressed, including exon-deleted variants (Δ), have not been determined in the monkey or human frontal cortex. Because the types of ERα mRNA expressed in brain could define neur...
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creator | Perlman, W.R. Matsumoto, M. Beltaifa, S. Hyde, T.M. Saunders, R.C. Webster, M.J. Rubinow, D.R. Kleinman, J.E. Weickert, C.S. |
description | Although estrogen receptor alpha (ERα) mRNA has been detected in the primate frontal cortex, the types of ERα transcripts expressed, including exon-deleted variants (Δ), have not been determined in the monkey or human frontal cortex. Because the types of ERα mRNA expressed in brain could define neuronal responses to estrogens, we examined the transcript pool of ERα mRNAs expressed in normal adult and developing human and macaque frontal cortex. We reverse transcribed total RNA from the postmortem frontal cortex of 29 normal adult humans, 12 rhesus macaques, and 19 people ranging from infants to adults and employed two rounds of nested polymerase chain reaction (PCR) to generate ERα products spanning the coding domain. In a third nested PCR, we used primers specific for novel sequences of exon–exon junctions created when whole exons are missing. By sequencing PCR products, we detected 60 instances of 12 distinct ΔERα mRNAs in adult humans and 94 instances of 13 distinct ΔERα mRNAs in monkeys in differing patterns from one individual to another. In adult humans, 83% of individuals expressed at least 1 ΔERα mRNA variant, and 100% of the monkeys expressed at least 1 ΔERα mRNA variant. The single Δ2, Δ5, and Δ7 variants were frequently expressed in both human and monkey frontal cortex, Δ3 variants were rare in both species, and Δ6 variants were more frequently expressed in monkeys. In both species, we detected double, triple and quadruple Δs, but these were less common than single Δs. The pattern of human variant expression did not appear to change dramatically as a function of age. These findings imply the potential to produce different ERα proteins in frontal cortex, possibly with altered structure and function which may have physiological relevance for gene transcription by virtue of altered functional interactions with each other, other steroid hormone receptors, and genomic DNA. |
doi_str_mv | 10.1016/j.neuroscience.2005.03.055 |
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Because the types of ERα mRNA expressed in brain could define neuronal responses to estrogens, we examined the transcript pool of ERα mRNAs expressed in normal adult and developing human and macaque frontal cortex. We reverse transcribed total RNA from the postmortem frontal cortex of 29 normal adult humans, 12 rhesus macaques, and 19 people ranging from infants to adults and employed two rounds of nested polymerase chain reaction (PCR) to generate ERα products spanning the coding domain. In a third nested PCR, we used primers specific for novel sequences of exon–exon junctions created when whole exons are missing. By sequencing PCR products, we detected 60 instances of 12 distinct ΔERα mRNAs in adult humans and 94 instances of 13 distinct ΔERα mRNAs in monkeys in differing patterns from one individual to another. In adult humans, 83% of individuals expressed at least 1 ΔERα mRNA variant, and 100% of the monkeys expressed at least 1 ΔERα mRNA variant. The single Δ2, Δ5, and Δ7 variants were frequently expressed in both human and monkey frontal cortex, Δ3 variants were rare in both species, and Δ6 variants were more frequently expressed in monkeys. In both species, we detected double, triple and quadruple Δs, but these were less common than single Δs. The pattern of human variant expression did not appear to change dramatically as a function of age. These findings imply the potential to produce different ERα proteins in frontal cortex, possibly with altered structure and function which may have physiological relevance for gene transcription by virtue of altered functional interactions with each other, other steroid hormone receptors, and genomic DNA.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2005.03.055</identifier><identifier>PMID: 15964702</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Age Factors ; Animals ; Biological and medical sciences ; Blotting, Northern ; brain ; Child ; Child, Preschool ; Chromosomes, Human, Pair 6 ; Estrogen Receptor alpha - genetics ; Estrogen Receptor alpha - metabolism ; Exons - genetics ; Female ; Frontal Lobe - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Deletion ; gene expression ; Gene Expression - physiology ; Gene Expression Regulation, Developmental - physiology ; hormone ; Humans ; Infant ; isoform ; Macaca mulatta ; Male ; Middle Aged ; monkey ; Primates ; Reverse Transcriptase Polymerase Chain Reaction - methods ; RNA, Messenger - metabolism ; Sex Factors ; splicing ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2005, Vol.134 (1), p.81-95</ispartof><rights>2005 IBRO</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-3c1f37da88750deb03392ac21b79150896445c7b99e3487008c06fc4c6f1db113</citedby><cites>FETCH-LOGICAL-c439t-3c1f37da88750deb03392ac21b79150896445c7b99e3487008c06fc4c6f1db113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S030645220500343X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17018754$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15964702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perlman, W.R.</creatorcontrib><creatorcontrib>Matsumoto, M.</creatorcontrib><creatorcontrib>Beltaifa, S.</creatorcontrib><creatorcontrib>Hyde, T.M.</creatorcontrib><creatorcontrib>Saunders, R.C.</creatorcontrib><creatorcontrib>Webster, M.J.</creatorcontrib><creatorcontrib>Rubinow, D.R.</creatorcontrib><creatorcontrib>Kleinman, J.E.</creatorcontrib><creatorcontrib>Weickert, C.S.</creatorcontrib><title>Expression of estrogen receptor alpha exon-deleted mRNA variants in the human and non-human primate frontal cortex</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Although estrogen receptor alpha (ERα) mRNA has been detected in the primate frontal cortex, the types of ERα transcripts expressed, including exon-deleted variants (Δ), have not been determined in the monkey or human frontal cortex. Because the types of ERα mRNA expressed in brain could define neuronal responses to estrogens, we examined the transcript pool of ERα mRNAs expressed in normal adult and developing human and macaque frontal cortex. We reverse transcribed total RNA from the postmortem frontal cortex of 29 normal adult humans, 12 rhesus macaques, and 19 people ranging from infants to adults and employed two rounds of nested polymerase chain reaction (PCR) to generate ERα products spanning the coding domain. In a third nested PCR, we used primers specific for novel sequences of exon–exon junctions created when whole exons are missing. By sequencing PCR products, we detected 60 instances of 12 distinct ΔERα mRNAs in adult humans and 94 instances of 13 distinct ΔERα mRNAs in monkeys in differing patterns from one individual to another. In adult humans, 83% of individuals expressed at least 1 ΔERα mRNA variant, and 100% of the monkeys expressed at least 1 ΔERα mRNA variant. The single Δ2, Δ5, and Δ7 variants were frequently expressed in both human and monkey frontal cortex, Δ3 variants were rare in both species, and Δ6 variants were more frequently expressed in monkeys. In both species, we detected double, triple and quadruple Δs, but these were less common than single Δs. The pattern of human variant expression did not appear to change dramatically as a function of age. These findings imply the potential to produce different ERα proteins in frontal cortex, possibly with altered structure and function which may have physiological relevance for gene transcription by virtue of altered functional interactions with each other, other steroid hormone receptors, and genomic DNA.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>brain</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosomes, Human, Pair 6</subject><subject>Estrogen Receptor alpha - genetics</subject><subject>Estrogen Receptor alpha - metabolism</subject><subject>Exons - genetics</subject><subject>Female</subject><subject>Frontal Lobe - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>gene expression</subject><subject>Gene Expression - physiology</subject><subject>Gene Expression Regulation, Developmental - physiology</subject><subject>hormone</subject><subject>Humans</subject><subject>Infant</subject><subject>isoform</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Middle Aged</subject><subject>monkey</subject><subject>Primates</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>RNA, Messenger - metabolism</subject><subject>Sex Factors</subject><subject>splicing</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV2L1TAQhoMo7vHoX5Ag6F3rpGma1rtld_2ARUH0OqTp1JNDm9QkXY7_3qynsN5pbkLgmcy88xDyikHJgDVvj6XDNfhoLDqDZQUgSuAlCPGI7FgreSFFXT8mO-DQFLWoqgvyLMYj5CNq_pRcMNE1tYRqR8LNaQkYo_WO-pFiTMH_QEcDGlySD1RPy0FTPHlXDDhhwoHOXz9f0jsdrHYpUutoOiA9rLN2VLuBuoyeX0uws05Ix-Bd0hM1PiQ8PSdPRj1FfLHde_L9_c23q4_F7ZcPn64ubwtT8y4V3LCRy0G3rRQwYA-cd5U2FetlxwS0OUEtjOy7DnndSoDWQDOa2jQjG3rG-J68Of-7BP9zzcnUbKPBadIO_RpV0wLrWFP9E2SSdbyGLoPvzqDJ248BR_UnYfilGKh7Neqo_laj7tUo4CqrycUvty5rP-PwULq5yMDrDdDR6GkM2hkbHzgJ2W32tyfXZw7z8u4sBrW1G2y2ltTg7f_M8xuyirRw</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>Perlman, W.R.</creator><creator>Matsumoto, M.</creator><creator>Beltaifa, S.</creator><creator>Hyde, T.M.</creator><creator>Saunders, R.C.</creator><creator>Webster, M.J.</creator><creator>Rubinow, D.R.</creator><creator>Kleinman, J.E.</creator><creator>Weickert, C.S.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>2005</creationdate><title>Expression of estrogen receptor alpha exon-deleted mRNA variants in the human and non-human primate frontal cortex</title><author>Perlman, W.R. ; Matsumoto, M. ; Beltaifa, S. ; Hyde, T.M. ; Saunders, R.C. ; Webster, M.J. ; Rubinow, D.R. ; Kleinman, J.E. ; Weickert, C.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-3c1f37da88750deb03392ac21b79150896445c7b99e3487008c06fc4c6f1db113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>brain</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromosomes, Human, Pair 6</topic><topic>Estrogen Receptor alpha - genetics</topic><topic>Estrogen Receptor alpha - metabolism</topic><topic>Exons - genetics</topic><topic>Female</topic><topic>Frontal Lobe - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Deletion</topic><topic>gene expression</topic><topic>Gene Expression - physiology</topic><topic>Gene Expression Regulation, Developmental - physiology</topic><topic>hormone</topic><topic>Humans</topic><topic>Infant</topic><topic>isoform</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>Middle Aged</topic><topic>monkey</topic><topic>Primates</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>RNA, Messenger - metabolism</topic><topic>Sex Factors</topic><topic>splicing</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perlman, W.R.</creatorcontrib><creatorcontrib>Matsumoto, M.</creatorcontrib><creatorcontrib>Beltaifa, S.</creatorcontrib><creatorcontrib>Hyde, T.M.</creatorcontrib><creatorcontrib>Saunders, R.C.</creatorcontrib><creatorcontrib>Webster, M.J.</creatorcontrib><creatorcontrib>Rubinow, D.R.</creatorcontrib><creatorcontrib>Kleinman, J.E.</creatorcontrib><creatorcontrib>Weickert, C.S.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perlman, W.R.</au><au>Matsumoto, M.</au><au>Beltaifa, S.</au><au>Hyde, T.M.</au><au>Saunders, R.C.</au><au>Webster, M.J.</au><au>Rubinow, D.R.</au><au>Kleinman, J.E.</au><au>Weickert, C.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of estrogen receptor alpha exon-deleted mRNA variants in the human and non-human primate frontal cortex</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2005</date><risdate>2005</risdate><volume>134</volume><issue>1</issue><spage>81</spage><epage>95</epage><pages>81-95</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Although estrogen receptor alpha (ERα) mRNA has been detected in the primate frontal cortex, the types of ERα transcripts expressed, including exon-deleted variants (Δ), have not been determined in the monkey or human frontal cortex. Because the types of ERα mRNA expressed in brain could define neuronal responses to estrogens, we examined the transcript pool of ERα mRNAs expressed in normal adult and developing human and macaque frontal cortex. We reverse transcribed total RNA from the postmortem frontal cortex of 29 normal adult humans, 12 rhesus macaques, and 19 people ranging from infants to adults and employed two rounds of nested polymerase chain reaction (PCR) to generate ERα products spanning the coding domain. In a third nested PCR, we used primers specific for novel sequences of exon–exon junctions created when whole exons are missing. By sequencing PCR products, we detected 60 instances of 12 distinct ΔERα mRNAs in adult humans and 94 instances of 13 distinct ΔERα mRNAs in monkeys in differing patterns from one individual to another. In adult humans, 83% of individuals expressed at least 1 ΔERα mRNA variant, and 100% of the monkeys expressed at least 1 ΔERα mRNA variant. The single Δ2, Δ5, and Δ7 variants were frequently expressed in both human and monkey frontal cortex, Δ3 variants were rare in both species, and Δ6 variants were more frequently expressed in monkeys. In both species, we detected double, triple and quadruple Δs, but these were less common than single Δs. The pattern of human variant expression did not appear to change dramatically as a function of age. These findings imply the potential to produce different ERα proteins in frontal cortex, possibly with altered structure and function which may have physiological relevance for gene transcription by virtue of altered functional interactions with each other, other steroid hormone receptors, and genomic DNA.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15964702</pmid><doi>10.1016/j.neuroscience.2005.03.055</doi><tpages>15</tpages></addata></record> |
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subjects | Adolescent Adult Age Factors Animals Biological and medical sciences Blotting, Northern brain Child Child, Preschool Chromosomes, Human, Pair 6 Estrogen Receptor alpha - genetics Estrogen Receptor alpha - metabolism Exons - genetics Female Frontal Lobe - metabolism Fundamental and applied biological sciences. Psychology Gene Deletion gene expression Gene Expression - physiology Gene Expression Regulation, Developmental - physiology hormone Humans Infant isoform Macaca mulatta Male Middle Aged monkey Primates Reverse Transcriptase Polymerase Chain Reaction - methods RNA, Messenger - metabolism Sex Factors splicing Vertebrates: nervous system and sense organs |
title | Expression of estrogen receptor alpha exon-deleted mRNA variants in the human and non-human primate frontal cortex |
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