Regeneration‐specific expression pattern of three posterior Hox genes
Homeobox genes encode positional information during primary and secondary axis formation during development. For this reason, the Hox genes have attracted attention in regeneration research as well. At early stages of regeneration, Hox genes have been implicated in wound healing and the dedifferenti...
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Veröffentlicht in: | Developmental dynamics 2003-02, Vol.226 (2), p.349-355 |
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description | Homeobox genes encode positional information during primary and secondary axis formation during development. For this reason, the Hox genes have attracted attention in regeneration research as well. At early stages of regeneration, Hox genes have been implicated in wound healing and the dedifferentiation process and at later stages in the patterning of the blastema. We studied the expression of three Abdominal B‐type Hox genes in Xenopus: XHoxc10, XHoxa13, and XHoxd13 during normal limb development and during regeneration of limbs and tails. We compared their expression with nonregenerating and with wounded limbs and tails, respectively. We show that the temporal and spatial control of these three Hox genes in blastemas differs from normal development. All three are specific to regeneration, XHoxc10 is up‐regulated at the right time and at the site where cells dedifferentiate and undifferentiated cells are recruited, whereas XHoxa13 is reexpressed slightly later in regeneration, when the blastemal cells proliferate and remains on during patterning of the blastema. XHoxd13 is not expressed until relatively late and appears to be involved only in patterning of the blastema. Developmental Dynamics 226:349–355, 2003.© 2003 Wiley‐Liss, Inc. |
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For this reason, the Hox genes have attracted attention in regeneration research as well. At early stages of regeneration, Hox genes have been implicated in wound healing and the dedifferentiation process and at later stages in the patterning of the blastema. We studied the expression of three Abdominal B‐type Hox genes in Xenopus: XHoxc10, XHoxa13, and XHoxd13 during normal limb development and during regeneration of limbs and tails. We compared their expression with nonregenerating and with wounded limbs and tails, respectively. We show that the temporal and spatial control of these three Hox genes in blastemas differs from normal development. All three are specific to regeneration, XHoxc10 is up‐regulated at the right time and at the site where cells dedifferentiate and undifferentiated cells are recruited, whereas XHoxa13 is reexpressed slightly later in regeneration, when the blastemal cells proliferate and remains on during patterning of the blastema. XHoxd13 is not expressed until relatively late and appears to be involved only in patterning of the blastema. Developmental Dynamics 226:349–355, 2003.© 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/dvdy.10231</identifier><identifier>PMID: 12557213</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aging - metabolism ; Animals ; Embryo, Nonmammalian - metabolism ; Extremities - growth & development ; Gene Expression ; Genes, Homeobox ; Homeodomain Proteins - genetics ; Hox genes ; Larva - metabolism ; regeneration ; Regeneration - genetics ; Tail - injuries ; Transcription Factors ; wounding ; Wounds, Penetrating - genetics ; Xenopus ; Xenopus - embryology ; Xenopus - genetics ; Xenopus - growth & development ; Xenopus Proteins</subject><ispartof>Developmental dynamics, 2003-02, Vol.226 (2), p.349-355</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4891-2f40b71af0552b38db502c55a84eb7addbac4001c74a83edad18e3de9d49a1553</citedby><cites>FETCH-LOGICAL-c4891-2f40b71af0552b38db502c55a84eb7addbac4001c74a83edad18e3de9d49a1553</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.10231$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdvdy.10231$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12557213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Christen, Bea</creatorcontrib><creatorcontrib>Beck, Caroline W.</creatorcontrib><creatorcontrib>Lombardo, Aurora</creatorcontrib><creatorcontrib>Slack, Jonathan M.W.</creatorcontrib><title>Regeneration‐specific expression pattern of three posterior Hox genes</title><title>Developmental dynamics</title><addtitle>Dev Dyn</addtitle><description>Homeobox genes encode positional information during primary and secondary axis formation during development. For this reason, the Hox genes have attracted attention in regeneration research as well. At early stages of regeneration, Hox genes have been implicated in wound healing and the dedifferentiation process and at later stages in the patterning of the blastema. We studied the expression of three Abdominal B‐type Hox genes in Xenopus: XHoxc10, XHoxa13, and XHoxd13 during normal limb development and during regeneration of limbs and tails. We compared their expression with nonregenerating and with wounded limbs and tails, respectively. We show that the temporal and spatial control of these three Hox genes in blastemas differs from normal development. All three are specific to regeneration, XHoxc10 is up‐regulated at the right time and at the site where cells dedifferentiate and undifferentiated cells are recruited, whereas XHoxa13 is reexpressed slightly later in regeneration, when the blastemal cells proliferate and remains on during patterning of the blastema. XHoxd13 is not expressed until relatively late and appears to be involved only in patterning of the blastema. Developmental Dynamics 226:349–355, 2003.© 2003 Wiley‐Liss, Inc.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Extremities - growth & development</subject><subject>Gene Expression</subject><subject>Genes, Homeobox</subject><subject>Homeodomain Proteins - genetics</subject><subject>Hox genes</subject><subject>Larva - metabolism</subject><subject>regeneration</subject><subject>Regeneration - genetics</subject><subject>Tail - injuries</subject><subject>Transcription Factors</subject><subject>wounding</subject><subject>Wounds, Penetrating - genetics</subject><subject>Xenopus</subject><subject>Xenopus - embryology</subject><subject>Xenopus - genetics</subject><subject>Xenopus - growth & development</subject><subject>Xenopus Proteins</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>eNqNkcFKxDAYhIMo7rp68QGkJw9CNUkTkx7F1V1hQRAVPIW0-auVblOTru7efASf0ScxtQve1NM_DN8_hxmE9gk-JhjTE_NqVkHRhGygIcGpiDERYrPTXMYykXKAdrx_xhjLU0a20YBQzgUlyRBNbuARanC6LW39-f7hG8jLoswjWDYOvA9u1Oi2BVdHtojaJwcQNdYHo7Qumtpl1P37XbRV6MrD3vqO0N3lxe35NJ5dT67Oz2ZxzmRKYlownAmiC8w5zRJpMo5pzrmWDDKhjcl0zjAmuWBaJmC0IRISA6lhqSacJyN02Oc2zr4swLdqXvocqkrXYBdeCZpKypj8E6ShHIpDB_8DQ7sjdNSDubPeOyhU48q5ditFsOqGUN0Q6nuIAB-sUxfZHMwPum4-AKQH3soKVr9EqfH9-KEP_QKcZJSF</recordid><startdate>200302</startdate><enddate>200302</enddate><creator>Christen, Bea</creator><creator>Beck, Caroline W.</creator><creator>Lombardo, Aurora</creator><creator>Slack, Jonathan M.W.</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>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200302</creationdate><title>Regeneration‐specific expression pattern of three posterior Hox genes</title><author>Christen, Bea ; Beck, Caroline W. ; Lombardo, Aurora ; Slack, Jonathan M.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4891-2f40b71af0552b38db502c55a84eb7addbac4001c74a83edad18e3de9d49a1553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aging - metabolism</topic><topic>Animals</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Extremities - growth & development</topic><topic>Gene Expression</topic><topic>Genes, Homeobox</topic><topic>Homeodomain Proteins - genetics</topic><topic>Hox genes</topic><topic>Larva - metabolism</topic><topic>regeneration</topic><topic>Regeneration - genetics</topic><topic>Tail - injuries</topic><topic>Transcription Factors</topic><topic>wounding</topic><topic>Wounds, Penetrating - genetics</topic><topic>Xenopus</topic><topic>Xenopus - embryology</topic><topic>Xenopus - genetics</topic><topic>Xenopus - growth & development</topic><topic>Xenopus Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Christen, Bea</creatorcontrib><creatorcontrib>Beck, Caroline W.</creatorcontrib><creatorcontrib>Lombardo, Aurora</creatorcontrib><creatorcontrib>Slack, Jonathan M.W.</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>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</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>Christen, Bea</au><au>Beck, Caroline W.</au><au>Lombardo, Aurora</au><au>Slack, Jonathan M.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regeneration‐specific expression pattern of three posterior Hox genes</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>2003-02</date><risdate>2003</risdate><volume>226</volume><issue>2</issue><spage>349</spage><epage>355</epage><pages>349-355</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><abstract>Homeobox genes encode positional information during primary and secondary axis formation during development. For this reason, the Hox genes have attracted attention in regeneration research as well. At early stages of regeneration, Hox genes have been implicated in wound healing and the dedifferentiation process and at later stages in the patterning of the blastema. We studied the expression of three Abdominal B‐type Hox genes in Xenopus: XHoxc10, XHoxa13, and XHoxd13 during normal limb development and during regeneration of limbs and tails. We compared their expression with nonregenerating and with wounded limbs and tails, respectively. We show that the temporal and spatial control of these three Hox genes in blastemas differs from normal development. All three are specific to regeneration, XHoxc10 is up‐regulated at the right time and at the site where cells dedifferentiate and undifferentiated cells are recruited, whereas XHoxa13 is reexpressed slightly later in regeneration, when the blastemal cells proliferate and remains on during patterning of the blastema. XHoxd13 is not expressed until relatively late and appears to be involved only in patterning of the blastema. Developmental Dynamics 226:349–355, 2003.© 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12557213</pmid><doi>10.1002/dvdy.10231</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging - metabolism Animals Embryo, Nonmammalian - metabolism Extremities - growth & development Gene Expression Genes, Homeobox Homeodomain Proteins - genetics Hox genes Larva - metabolism regeneration Regeneration - genetics Tail - injuries Transcription Factors wounding Wounds, Penetrating - genetics Xenopus Xenopus - embryology Xenopus - genetics Xenopus - growth & development Xenopus Proteins |
title | Regeneration‐specific expression pattern of three posterior Hox genes |
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