Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1

Human mast cell tryptases vary strikingly in secretion, catalytic competence, and inheritance. To explore the basis of variation, we compared genes from a range of primates, including humans, great apes (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosim...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of immunology (1950) 2007-11, Vol.179 (9), p.6072-6079
Hauptverfasser: Trivedi, Neil N., Tong, Qiao, Raman, Kavita, Bhagwandin, Vikash J., Caughey, George H.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6079
container_issue 9
container_start_page 6072
container_title The Journal of immunology (1950)
container_volume 179
creator Trivedi, Neil N.
Tong, Qiao
Raman, Kavita
Bhagwandin, Vikash J.
Caughey, George H.
description Human mast cell tryptases vary strikingly in secretion, catalytic competence, and inheritance. To explore the basis of variation, we compared genes from a range of primates, including humans, great apes (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosimian (galago), tracking key changes. Our analysis reveals that extant soluble tryptase-like proteins, including α - and β -like tryptases, mastins, and implantation serine proteases, likely evolved from membrane-anchored ancestors because their more deeply rooted relatives ( γ tryptases, pancreasins, prostasins) are type I transmembrane peptidases. Function-altering mutations appeared at widely separated times during primate speciation, with tryptases evolving by duplication, gene conversion, and point mutation. The α -tryptase Gly 216 Asp catalytic domain mutation, which diminishes activity, is present in macaque tryptases, and thus arose before great apes and Old World monkeys shared an ancestor, and before the α β split. However, the Arg– 3 Gln processing mutation appeared recently, affecting only human α . By comparison, the transmembrane γ -tryptase gene, which anchors the telomeric end of the multigene tryptase locus, changed little during primate evolution. Related transmembrane peptidase genes were found in reptiles, amphibians, and fish. We identified soluble tryptase-like genes in the full spectrum of mammals, including marsupial (opossum) and monotreme (platypus), but not in nonmammalian vertebrates. Overall, our analysis suggests that soluble tryptases evolved rapidly from membrane-anchored, two-chain peptidases in ancestral vertebrates into soluble, single-chain, self-compartmentalizing, inhibitor-resistant oligomers expressed primarily by mast cells, and that much of present numerical, behavioral, and genetic diversity of α - and β -like tryptases was acquired during primate evolution.
format Article
fullrecord <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2366170</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_2366170</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_23661703</originalsourceid><addsrcrecordid>eNqljk1OwzAUhC0EouHnDu8Ckey0dWCDhKIiFiBVULGNXuPX1OA4lu1Gyjk4CXCPnKlpxYY1q1nMfJ_mhCViPueplFyesoTzLEtFLvMJuwjhnXMueTY7ZxOR385yeSMS9vmMIUJBxsDwBWgVDN-w8r2LGChAsUVbk4IXdFqZHtTOa1vD0usGI8Gro0pj1K09oouuNd243vi2geEnfdIfNMrQhoaa9ZgES3JRq6NbW7i3FYXo0cAb-UjjJFIQV-xsgybQ9W9esruHxap4TN1u3ZCqyB6Q0h1O-L5sUZd_G6u3Zd12ZTaVUuR8-m_BHgzjc2U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Trivedi, Neil N. ; Tong, Qiao ; Raman, Kavita ; Bhagwandin, Vikash J. ; Caughey, George H.</creator><creatorcontrib>Trivedi, Neil N. ; Tong, Qiao ; Raman, Kavita ; Bhagwandin, Vikash J. ; Caughey, George H.</creatorcontrib><description>Human mast cell tryptases vary strikingly in secretion, catalytic competence, and inheritance. To explore the basis of variation, we compared genes from a range of primates, including humans, great apes (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosimian (galago), tracking key changes. Our analysis reveals that extant soluble tryptase-like proteins, including α - and β -like tryptases, mastins, and implantation serine proteases, likely evolved from membrane-anchored ancestors because their more deeply rooted relatives ( γ tryptases, pancreasins, prostasins) are type I transmembrane peptidases. Function-altering mutations appeared at widely separated times during primate speciation, with tryptases evolving by duplication, gene conversion, and point mutation. The α -tryptase Gly 216 Asp catalytic domain mutation, which diminishes activity, is present in macaque tryptases, and thus arose before great apes and Old World monkeys shared an ancestor, and before the α β split. However, the Arg– 3 Gln processing mutation appeared recently, affecting only human α . By comparison, the transmembrane γ -tryptase gene, which anchors the telomeric end of the multigene tryptase locus, changed little during primate evolution. Related transmembrane peptidase genes were found in reptiles, amphibians, and fish. We identified soluble tryptase-like genes in the full spectrum of mammals, including marsupial (opossum) and monotreme (platypus), but not in nonmammalian vertebrates. Overall, our analysis suggests that soluble tryptases evolved rapidly from membrane-anchored, two-chain peptidases in ancestral vertebrates into soluble, single-chain, self-compartmentalizing, inhibitor-resistant oligomers expressed primarily by mast cells, and that much of present numerical, behavioral, and genetic diversity of α - and β -like tryptases was acquired during primate evolution.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>PMID: 17947681</identifier><language>eng</language><ispartof>The Journal of immunology (1950), 2007-11, Vol.179 (9), p.6072-6079</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885</link.rule.ids></links><search><creatorcontrib>Trivedi, Neil N.</creatorcontrib><creatorcontrib>Tong, Qiao</creatorcontrib><creatorcontrib>Raman, Kavita</creatorcontrib><creatorcontrib>Bhagwandin, Vikash J.</creatorcontrib><creatorcontrib>Caughey, George H.</creatorcontrib><title>Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1</title><title>The Journal of immunology (1950)</title><description>Human mast cell tryptases vary strikingly in secretion, catalytic competence, and inheritance. To explore the basis of variation, we compared genes from a range of primates, including humans, great apes (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosimian (galago), tracking key changes. Our analysis reveals that extant soluble tryptase-like proteins, including α - and β -like tryptases, mastins, and implantation serine proteases, likely evolved from membrane-anchored ancestors because their more deeply rooted relatives ( γ tryptases, pancreasins, prostasins) are type I transmembrane peptidases. Function-altering mutations appeared at widely separated times during primate speciation, with tryptases evolving by duplication, gene conversion, and point mutation. The α -tryptase Gly 216 Asp catalytic domain mutation, which diminishes activity, is present in macaque tryptases, and thus arose before great apes and Old World monkeys shared an ancestor, and before the α β split. However, the Arg– 3 Gln processing mutation appeared recently, affecting only human α . By comparison, the transmembrane γ -tryptase gene, which anchors the telomeric end of the multigene tryptase locus, changed little during primate evolution. Related transmembrane peptidase genes were found in reptiles, amphibians, and fish. We identified soluble tryptase-like genes in the full spectrum of mammals, including marsupial (opossum) and monotreme (platypus), but not in nonmammalian vertebrates. Overall, our analysis suggests that soluble tryptases evolved rapidly from membrane-anchored, two-chain peptidases in ancestral vertebrates into soluble, single-chain, self-compartmentalizing, inhibitor-resistant oligomers expressed primarily by mast cells, and that much of present numerical, behavioral, and genetic diversity of α - and β -like tryptases was acquired during primate evolution.</description><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqljk1OwzAUhC0EouHnDu8Ckey0dWCDhKIiFiBVULGNXuPX1OA4lu1Gyjk4CXCPnKlpxYY1q1nMfJ_mhCViPueplFyesoTzLEtFLvMJuwjhnXMueTY7ZxOR385yeSMS9vmMIUJBxsDwBWgVDN-w8r2LGChAsUVbk4IXdFqZHtTOa1vD0usGI8Gro0pj1K09oouuNd243vi2geEnfdIfNMrQhoaa9ZgES3JRq6NbW7i3FYXo0cAb-UjjJFIQV-xsgybQ9W9esruHxap4TN1u3ZCqyB6Q0h1O-L5sUZd_G6u3Zd12ZTaVUuR8-m_BHgzjc2U</recordid><startdate>20071101</startdate><enddate>20071101</enddate><creator>Trivedi, Neil N.</creator><creator>Tong, Qiao</creator><creator>Raman, Kavita</creator><creator>Bhagwandin, Vikash J.</creator><creator>Caughey, George H.</creator><scope>5PM</scope></search><sort><creationdate>20071101</creationdate><title>Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1</title><author>Trivedi, Neil N. ; Tong, Qiao ; Raman, Kavita ; Bhagwandin, Vikash J. ; Caughey, George H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_23661703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trivedi, Neil N.</creatorcontrib><creatorcontrib>Tong, Qiao</creatorcontrib><creatorcontrib>Raman, Kavita</creatorcontrib><creatorcontrib>Bhagwandin, Vikash J.</creatorcontrib><creatorcontrib>Caughey, George H.</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trivedi, Neil N.</au><au>Tong, Qiao</au><au>Raman, Kavita</au><au>Bhagwandin, Vikash J.</au><au>Caughey, George H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1</atitle><jtitle>The Journal of immunology (1950)</jtitle><date>2007-11-01</date><risdate>2007</risdate><volume>179</volume><issue>9</issue><spage>6072</spage><epage>6079</epage><pages>6072-6079</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Human mast cell tryptases vary strikingly in secretion, catalytic competence, and inheritance. To explore the basis of variation, we compared genes from a range of primates, including humans, great apes (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosimian (galago), tracking key changes. Our analysis reveals that extant soluble tryptase-like proteins, including α - and β -like tryptases, mastins, and implantation serine proteases, likely evolved from membrane-anchored ancestors because their more deeply rooted relatives ( γ tryptases, pancreasins, prostasins) are type I transmembrane peptidases. Function-altering mutations appeared at widely separated times during primate speciation, with tryptases evolving by duplication, gene conversion, and point mutation. The α -tryptase Gly 216 Asp catalytic domain mutation, which diminishes activity, is present in macaque tryptases, and thus arose before great apes and Old World monkeys shared an ancestor, and before the α β split. However, the Arg– 3 Gln processing mutation appeared recently, affecting only human α . By comparison, the transmembrane γ -tryptase gene, which anchors the telomeric end of the multigene tryptase locus, changed little during primate evolution. Related transmembrane peptidase genes were found in reptiles, amphibians, and fish. We identified soluble tryptase-like genes in the full spectrum of mammals, including marsupial (opossum) and monotreme (platypus), but not in nonmammalian vertebrates. Overall, our analysis suggests that soluble tryptases evolved rapidly from membrane-anchored, two-chain peptidases in ancestral vertebrates into soluble, single-chain, self-compartmentalizing, inhibitor-resistant oligomers expressed primarily by mast cells, and that much of present numerical, behavioral, and genetic diversity of α - and β -like tryptases was acquired during primate evolution.</abstract><pmid>17947681</pmid></addata></record>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 2007-11, Vol.179 (9), p.6072-6079
issn 0022-1767
1550-6606
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2366170
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
title Mast Cell α and β Tryptases Changed Rapidly during Primate Speciation and Evolved from γ-Like Transmembrane Peptidases in Ancestral Vertebrates1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T08%3A41%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mast%20Cell%20%CE%B1%20and%20%CE%B2%20Tryptases%20Changed%20Rapidly%20during%20Primate%20Speciation%20and%20Evolved%20from%20%CE%B3-Like%20Transmembrane%20Peptidases%20in%20Ancestral%20Vertebrates1&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Trivedi,%20Neil%20N.&rft.date=2007-11-01&rft.volume=179&rft.issue=9&rft.spage=6072&rft.epage=6079&rft.pages=6072-6079&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/&rft_dat=%3Cpubmedcentral%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_2366170%3C/pubmedcentral%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/17947681&rfr_iscdi=true