Cardiac Troponin I Is a Heart-Specific Marker in the Xenopus Embryo: Expression during Abnormal Heart Morphogenesis
Cardiac troponin I (troponin Ic) expression is restricted to the heart at all stages of Xenopus development. Whole-mount in situ hybridization and Northern blot analysis indicates that troponin Ic is first expressed in tailbud embryos (stage 28) about the time of the first cytological heart differen...
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Veröffentlicht in: | Developmental biology 1994-10, Vol.165 (2), p.432-441 |
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creator | Drysdale, Thomas A. Tonissen, Kathryn F. Patterson, Kristin D. Crawford, Michael J. Krieg, Paul A. |
description | Cardiac troponin I (troponin Ic) expression is restricted to the heart at all stages of Xenopus development. Whole-mount in situ hybridization and Northern blot analysis indicates that troponin Ic is first expressed in tailbud embryos (stage 28) about the time of the first cytological heart differentiation and about 24 hr before beating tissue is observed. We have used this marker to examine abnormal heart morphogenesis in embryos treated with retinoic acid and lithium. When retinoic acid is administered to embryos prior to heart specification, heart tissue is reduced and often completely ablated. When embryos are treated after heart specification, but before the heart primordium migrates to the ventral midline, the migration is unaffected but smaller, abnormal hearts result. Lithium treatment of cleavage stage embryos causes an increase in heart tissue. In severely dorsalized embryos, heart tissue can be found around the entire embryo with the exception of a small gap at the most dorsal point. This gap indicates that migration of the heart to the ventral midline does not occur in these embryos. Later in development, a centrally located, beating heart is observed in dorsalized embryos. The timing of its appearance suggests that it is formed by movements normally associated with heart morphogenesis rather than migration. |
doi_str_mv | 10.1006/dbio.1994.1265 |
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Whole-mount in situ hybridization and Northern blot analysis indicates that troponin Ic is first expressed in tailbud embryos (stage 28) about the time of the first cytological heart differentiation and about 24 hr before beating tissue is observed. We have used this marker to examine abnormal heart morphogenesis in embryos treated with retinoic acid and lithium. When retinoic acid is administered to embryos prior to heart specification, heart tissue is reduced and often completely ablated. When embryos are treated after heart specification, but before the heart primordium migrates to the ventral midline, the migration is unaffected but smaller, abnormal hearts result. Lithium treatment of cleavage stage embryos causes an increase in heart tissue. In severely dorsalized embryos, heart tissue can be found around the entire embryo with the exception of a small gap at the most dorsal point. This gap indicates that migration of the heart to the ventral midline does not occur in these embryos. Later in development, a centrally located, beating heart is observed in dorsalized embryos. The timing of its appearance suggests that it is formed by movements normally associated with heart morphogenesis rather than migration.</description><identifier>ISSN: 0012-1606</identifier><identifier>EISSN: 1095-564X</identifier><identifier>DOI: 10.1006/dbio.1994.1265</identifier><identifier>PMID: 7958411</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Base Sequence ; Biomarkers ; Cloning, Molecular ; DNA Primers - chemistry ; Freshwater ; Gene Expression ; Heart - embryology ; Heart Defects, Congenital - chemically induced ; In Situ Hybridization ; Lithium - pharmacology ; Molecular Sequence Data ; Morphogenesis - drug effects ; Myocardium - metabolism ; RNA, Messenger - genetics ; Tretinoin - pharmacology ; Troponin - metabolism ; Troponin I ; Xenopus ; Xenopus laevis - embryology</subject><ispartof>Developmental biology, 1994-10, Vol.165 (2), p.432-441</ispartof><rights>1994 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-fd88dc00949beb5cb90c279f9d6d05713258d622f4a33318492d9ace4e3689523</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/dbio.1994.1265$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7958411$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Drysdale, Thomas A.</creatorcontrib><creatorcontrib>Tonissen, Kathryn F.</creatorcontrib><creatorcontrib>Patterson, Kristin D.</creatorcontrib><creatorcontrib>Crawford, Michael J.</creatorcontrib><creatorcontrib>Krieg, Paul A.</creatorcontrib><title>Cardiac Troponin I Is a Heart-Specific Marker in the Xenopus Embryo: Expression during Abnormal Heart Morphogenesis</title><title>Developmental biology</title><addtitle>Dev Biol</addtitle><description>Cardiac troponin I (troponin Ic) expression is restricted to the heart at all stages of Xenopus development. Whole-mount in situ hybridization and Northern blot analysis indicates that troponin Ic is first expressed in tailbud embryos (stage 28) about the time of the first cytological heart differentiation and about 24 hr before beating tissue is observed. We have used this marker to examine abnormal heart morphogenesis in embryos treated with retinoic acid and lithium. When retinoic acid is administered to embryos prior to heart specification, heart tissue is reduced and often completely ablated. When embryos are treated after heart specification, but before the heart primordium migrates to the ventral midline, the migration is unaffected but smaller, abnormal hearts result. Lithium treatment of cleavage stage embryos causes an increase in heart tissue. In severely dorsalized embryos, heart tissue can be found around the entire embryo with the exception of a small gap at the most dorsal point. This gap indicates that migration of the heart to the ventral midline does not occur in these embryos. Later in development, a centrally located, beating heart is observed in dorsalized embryos. The timing of its appearance suggests that it is formed by movements normally associated with heart morphogenesis rather than migration.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biomarkers</subject><subject>Cloning, Molecular</subject><subject>DNA Primers - chemistry</subject><subject>Freshwater</subject><subject>Gene Expression</subject><subject>Heart - embryology</subject><subject>Heart Defects, Congenital - chemically induced</subject><subject>In Situ Hybridization</subject><subject>Lithium - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>Morphogenesis - drug effects</subject><subject>Myocardium - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>Tretinoin - pharmacology</subject><subject>Troponin - metabolism</subject><subject>Troponin I</subject><subject>Xenopus</subject><subject>Xenopus laevis - embryology</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFP3DAQha0KBFvaa29IPnHL1o7jxOaGVktZCdQDVOJmOfYEXDZ2GCcV_Huy2hW3nubw3vuk-Qj5wdmSM1b_9G1IS651teRlLb-QBWdaFrKuHo_IgjFeFrxm9Sn5mvNfxphQSpyQk0ZLVXG-IHll0Qfr6AOmIcUQ6YZuMrX0BiyOxf0ALnTB0TuLL4B0zsdnoI8Q0zBluu5bfE-XdP02IOQcUqR-whCf6FUbE_Z2u-fQu4TDc3qCCDnkb-S4s9sM3w_3jPy5Xj-sborb3782q6vbwomGjUXnlfKOMV3pFlrpWs1c2ehO-9oz2XBRSuXrsuwqK4TgqtKl19ZBBaJWWpbijFzsuQOm1wnyaPqQHWy3NkKasuENq4SUai4u90WHKWeEzgwYeovvhjOzs2x2ls3OstlZngfnB_LU9uA_6wetc672Oczv_QuAJrsA0YEPCG40PoX_oT8ApzSL5Q</recordid><startdate>19941001</startdate><enddate>19941001</enddate><creator>Drysdale, Thomas A.</creator><creator>Tonissen, Kathryn F.</creator><creator>Patterson, Kristin D.</creator><creator>Crawford, Michael J.</creator><creator>Krieg, Paul A.</creator><general>Elsevier Inc</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>7TM</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>19941001</creationdate><title>Cardiac Troponin I Is a Heart-Specific Marker in the Xenopus Embryo: Expression during Abnormal Heart Morphogenesis</title><author>Drysdale, Thomas A. ; Tonissen, Kathryn F. ; Patterson, Kristin D. ; Crawford, Michael J. ; Krieg, Paul A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-fd88dc00949beb5cb90c279f9d6d05713258d622f4a33318492d9ace4e3689523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Biomarkers</topic><topic>Cloning, Molecular</topic><topic>DNA Primers - chemistry</topic><topic>Freshwater</topic><topic>Gene Expression</topic><topic>Heart - embryology</topic><topic>Heart Defects, Congenital - chemically induced</topic><topic>In Situ Hybridization</topic><topic>Lithium - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>Morphogenesis - drug effects</topic><topic>Myocardium - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>Tretinoin - pharmacology</topic><topic>Troponin - metabolism</topic><topic>Troponin I</topic><topic>Xenopus</topic><topic>Xenopus laevis - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Drysdale, Thomas A.</creatorcontrib><creatorcontrib>Tonissen, Kathryn F.</creatorcontrib><creatorcontrib>Patterson, Kristin D.</creatorcontrib><creatorcontrib>Crawford, Michael J.</creatorcontrib><creatorcontrib>Krieg, Paul A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Drysdale, Thomas A.</au><au>Tonissen, Kathryn F.</au><au>Patterson, Kristin D.</au><au>Crawford, Michael J.</au><au>Krieg, Paul A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac Troponin I Is a Heart-Specific Marker in the Xenopus Embryo: Expression during Abnormal Heart Morphogenesis</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>1994-10-01</date><risdate>1994</risdate><volume>165</volume><issue>2</issue><spage>432</spage><epage>441</epage><pages>432-441</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><abstract>Cardiac troponin I (troponin Ic) expression is restricted to the heart at all stages of Xenopus development. Whole-mount in situ hybridization and Northern blot analysis indicates that troponin Ic is first expressed in tailbud embryos (stage 28) about the time of the first cytological heart differentiation and about 24 hr before beating tissue is observed. We have used this marker to examine abnormal heart morphogenesis in embryos treated with retinoic acid and lithium. When retinoic acid is administered to embryos prior to heart specification, heart tissue is reduced and often completely ablated. When embryos are treated after heart specification, but before the heart primordium migrates to the ventral midline, the migration is unaffected but smaller, abnormal hearts result. Lithium treatment of cleavage stage embryos causes an increase in heart tissue. In severely dorsalized embryos, heart tissue can be found around the entire embryo with the exception of a small gap at the most dorsal point. This gap indicates that migration of the heart to the ventral midline does not occur in these embryos. Later in development, a centrally located, beating heart is observed in dorsalized embryos. The timing of its appearance suggests that it is formed by movements normally associated with heart morphogenesis rather than migration.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>7958411</pmid><doi>10.1006/dbio.1994.1265</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Base Sequence Biomarkers Cloning, Molecular DNA Primers - chemistry Freshwater Gene Expression Heart - embryology Heart Defects, Congenital - chemically induced In Situ Hybridization Lithium - pharmacology Molecular Sequence Data Morphogenesis - drug effects Myocardium - metabolism RNA, Messenger - genetics Tretinoin - pharmacology Troponin - metabolism Troponin I Xenopus Xenopus laevis - embryology |
title | Cardiac Troponin I Is a Heart-Specific Marker in the Xenopus Embryo: Expression during Abnormal Heart Morphogenesis |
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