The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins
Cardiac development requires the action of transcription factors, which control the specification and differentiation of cardiac cell types. One of these factors, encoded by the homeobox gene tinman ( tin), is essential for the specification of all cardiac cells in Drosophila. An increasing number o...
Gespeichert in:
Veröffentlicht in: | Biochemical and biophysical research communications 2005-08, Vol.334 (2), p.361-369 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 369 |
---|---|
container_issue | 2 |
container_start_page | 361 |
container_title | Biochemical and biophysical research communications |
container_volume | 334 |
creator | Zaffran, Stéphane Frasch, Manfred |
description | Cardiac development requires the action of transcription factors, which control the specification and differentiation of cardiac cell types. One of these factors, encoded by the homeobox gene
tinman (
tin), is essential for the specification of all cardiac cells in
Drosophila. An increasing number of examples show that protein–protein interactions can be important for determining the specific transcriptional activities of homeodomain proteins, in addition to their binding to specific DNA target sites. Here, we show that Tin and Bagpipe (Bap), another homeodomain protein, form homo- and heterodimeric complexes. We demonstrate that homo- and heterodimerization of Tin is mediated through its homeodomain and that the region required for this interaction corresponds to the first two helices that are also necessary for DNA binding. We further show that, in the yeast system, the homeodomain can function as a transcriptional repressor domain. These findings suggest that protein–protein interactions of Tin play a role in its transcriptional and developmental functions. |
doi_str_mv | 10.1016/j.bbrc.2005.06.090 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00117156v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X05013239</els_id><sourcerecordid>17560002</sourcerecordid><originalsourceid>FETCH-LOGICAL-c419t-b599193ad992dabefea707c9825d28ce89f3fb6f481939cd16cac05fd3833cfc3</originalsourceid><addsrcrecordid>eNqFkU1LxDAQhoMoun78AQ_Sk-ChddKPtAEvIn7hopcVvIU0mbBZto0mXUF_vam76E1PA8kzw8z7EHJMIaNA2fkia1uvshygyoBlwGGLTGgsaU6h3CYTAGBpzunLHtkPYQFAacn4LtmjDKDkNUzI42yOydx16LTrpO0TZ5KZ7TvZJx1qKwcM47dLE9nrZI4Deqdth95-ysG6b_7xIXn1bkDbh0OyY-Qy4NGmHpDnm-vZ1V06fbq9v7qcpqqkfEjbinPKC6k5z7Vs0aCsoVa8ySudNwobbgrTMlM2keJKU6akgsrooikKZVRxQM7Wc-dyKV697aT_EE5acXc5FePbeGtNK_ZOI3u6ZuOSbysMg-hsULhcyh7dKgjWACtZkf8L0rqKucEI5mtQeReCR_OzAgUxqhELMaoRoxoBTEQnselkM33Vxmh_WzYuInCxBjAG927Ri6As9ipq8KgGoZ39a_4XIy-e2w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17560002</pqid></control><display><type>article</type><title>The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Zaffran, Stéphane ; Frasch, Manfred</creator><creatorcontrib>Zaffran, Stéphane ; Frasch, Manfred</creatorcontrib><description>Cardiac development requires the action of transcription factors, which control the specification and differentiation of cardiac cell types. One of these factors, encoded by the homeobox gene
tinman (
tin), is essential for the specification of all cardiac cells in
Drosophila. An increasing number of examples show that protein–protein interactions can be important for determining the specific transcriptional activities of homeodomain proteins, in addition to their binding to specific DNA target sites. Here, we show that Tin and Bagpipe (Bap), another homeodomain protein, form homo- and heterodimeric complexes. We demonstrate that homo- and heterodimerization of Tin is mediated through its homeodomain and that the region required for this interaction corresponds to the first two helices that are also necessary for DNA binding. We further show that, in the yeast system, the homeodomain can function as a transcriptional repressor domain. These findings suggest that protein–protein interactions of Tin play a role in its transcriptional and developmental functions.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2005.06.090</identifier><identifier>PMID: 16004970</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Binding Sites ; Cardiac ; Cellular Biology ; Dimerization ; Drosophila ; Drosophila Proteins - chemistry ; Drosophila Proteins - metabolism ; Homeodomain ; Homeodomain Proteins - chemistry ; Homeodomain Proteins - metabolism ; Life Sciences ; NK-2 ; Protein Binding ; Protein Interaction Mapping ; Protein Structure, Tertiary ; Repressor Proteins - chemistry ; Repressor Proteins - metabolism ; Structure-Activity Relationship ; Tinman ; Trans-Activators - chemistry ; Trans-Activators - metabolism ; Transcription Factors - chemistry ; Transcription Factors - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2005-08, Vol.334 (2), p.361-369</ispartof><rights>2005 Elsevier Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-b599193ad992dabefea707c9825d28ce89f3fb6f481939cd16cac05fd3833cfc3</citedby><cites>FETCH-LOGICAL-c419t-b599193ad992dabefea707c9825d28ce89f3fb6f481939cd16cac05fd3833cfc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2005.06.090$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16004970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00117156$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Zaffran, Stéphane</creatorcontrib><creatorcontrib>Frasch, Manfred</creatorcontrib><title>The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Cardiac development requires the action of transcription factors, which control the specification and differentiation of cardiac cell types. One of these factors, encoded by the homeobox gene
tinman (
tin), is essential for the specification of all cardiac cells in
Drosophila. An increasing number of examples show that protein–protein interactions can be important for determining the specific transcriptional activities of homeodomain proteins, in addition to their binding to specific DNA target sites. Here, we show that Tin and Bagpipe (Bap), another homeodomain protein, form homo- and heterodimeric complexes. We demonstrate that homo- and heterodimerization of Tin is mediated through its homeodomain and that the region required for this interaction corresponds to the first two helices that are also necessary for DNA binding. We further show that, in the yeast system, the homeodomain can function as a transcriptional repressor domain. These findings suggest that protein–protein interactions of Tin play a role in its transcriptional and developmental functions.</description><subject>Binding Sites</subject><subject>Cardiac</subject><subject>Cellular Biology</subject><subject>Dimerization</subject><subject>Drosophila</subject><subject>Drosophila Proteins - chemistry</subject><subject>Drosophila Proteins - metabolism</subject><subject>Homeodomain</subject><subject>Homeodomain Proteins - chemistry</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Life Sciences</subject><subject>NK-2</subject><subject>Protein Binding</subject><subject>Protein Interaction Mapping</subject><subject>Protein Structure, Tertiary</subject><subject>Repressor Proteins - chemistry</subject><subject>Repressor Proteins - metabolism</subject><subject>Structure-Activity Relationship</subject><subject>Tinman</subject><subject>Trans-Activators - chemistry</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - chemistry</subject><subject>Transcription Factors - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1LxDAQhoMoun78AQ_Sk-ChddKPtAEvIn7hopcVvIU0mbBZto0mXUF_vam76E1PA8kzw8z7EHJMIaNA2fkia1uvshygyoBlwGGLTGgsaU6h3CYTAGBpzunLHtkPYQFAacn4LtmjDKDkNUzI42yOydx16LTrpO0TZ5KZ7TvZJx1qKwcM47dLE9nrZI4Deqdth95-ysG6b_7xIXn1bkDbh0OyY-Qy4NGmHpDnm-vZ1V06fbq9v7qcpqqkfEjbinPKC6k5z7Vs0aCsoVa8ySudNwobbgrTMlM2keJKU6akgsrooikKZVRxQM7Wc-dyKV697aT_EE5acXc5FePbeGtNK_ZOI3u6ZuOSbysMg-hsULhcyh7dKgjWACtZkf8L0rqKucEI5mtQeReCR_OzAgUxqhELMaoRoxoBTEQnselkM33Vxmh_WzYuInCxBjAG927Ri6As9ipq8KgGoZ39a_4XIy-e2w</recordid><startdate>20050826</startdate><enddate>20050826</enddate><creator>Zaffran, Stéphane</creator><creator>Frasch, Manfred</creator><general>Elsevier Inc</general><general>Elsevier</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>7SS</scope><scope>7TM</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>20050826</creationdate><title>The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins</title><author>Zaffran, Stéphane ; Frasch, Manfred</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-b599193ad992dabefea707c9825d28ce89f3fb6f481939cd16cac05fd3833cfc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Binding Sites</topic><topic>Cardiac</topic><topic>Cellular Biology</topic><topic>Dimerization</topic><topic>Drosophila</topic><topic>Drosophila Proteins - chemistry</topic><topic>Drosophila Proteins - metabolism</topic><topic>Homeodomain</topic><topic>Homeodomain Proteins - chemistry</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Life Sciences</topic><topic>NK-2</topic><topic>Protein Binding</topic><topic>Protein Interaction Mapping</topic><topic>Protein Structure, Tertiary</topic><topic>Repressor Proteins - chemistry</topic><topic>Repressor Proteins - metabolism</topic><topic>Structure-Activity Relationship</topic><topic>Tinman</topic><topic>Trans-Activators - chemistry</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors - chemistry</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaffran, Stéphane</creatorcontrib><creatorcontrib>Frasch, Manfred</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaffran, Stéphane</au><au>Frasch, Manfred</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2005-08-26</date><risdate>2005</risdate><volume>334</volume><issue>2</issue><spage>361</spage><epage>369</epage><pages>361-369</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Cardiac development requires the action of transcription factors, which control the specification and differentiation of cardiac cell types. One of these factors, encoded by the homeobox gene
tinman (
tin), is essential for the specification of all cardiac cells in
Drosophila. An increasing number of examples show that protein–protein interactions can be important for determining the specific transcriptional activities of homeodomain proteins, in addition to their binding to specific DNA target sites. Here, we show that Tin and Bagpipe (Bap), another homeodomain protein, form homo- and heterodimeric complexes. We demonstrate that homo- and heterodimerization of Tin is mediated through its homeodomain and that the region required for this interaction corresponds to the first two helices that are also necessary for DNA binding. We further show that, in the yeast system, the homeodomain can function as a transcriptional repressor domain. These findings suggest that protein–protein interactions of Tin play a role in its transcriptional and developmental functions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16004970</pmid><doi>10.1016/j.bbrc.2005.06.090</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-291X |
ispartof | Biochemical and biophysical research communications, 2005-08, Vol.334 (2), p.361-369 |
issn | 0006-291X 1090-2104 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_00117156v1 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Binding Sites Cardiac Cellular Biology Dimerization Drosophila Drosophila Proteins - chemistry Drosophila Proteins - metabolism Homeodomain Homeodomain Proteins - chemistry Homeodomain Proteins - metabolism Life Sciences NK-2 Protein Binding Protein Interaction Mapping Protein Structure, Tertiary Repressor Proteins - chemistry Repressor Proteins - metabolism Structure-Activity Relationship Tinman Trans-Activators - chemistry Trans-Activators - metabolism Transcription Factors - chemistry Transcription Factors - metabolism |
title | The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T10%3A07%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20homeodomain%20of%20Tinman%20mediates%20homo-%20and%20heterodimerization%20of%20NK%20proteins&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Zaffran,%20St%C3%A9phane&rft.date=2005-08-26&rft.volume=334&rft.issue=2&rft.spage=361&rft.epage=369&rft.pages=361-369&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2005.06.090&rft_dat=%3Cproquest_hal_p%3E17560002%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17560002&rft_id=info:pmid/16004970&rft_els_id=S0006291X05013239&rfr_iscdi=true |