The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans
The development of the single cell layer skin or hypodermis of Caenorhabditis elegans is an excellent model for understanding cell fate specification and differentiation. Early in C. elegans embryogenesis, six rows of hypodermal cells adopt dorsal, lateral or ventral fates that go on to display dist...
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description | The development of the single cell layer skin or hypodermis of Caenorhabditis elegans is an excellent model for understanding cell fate specification and differentiation. Early in C. elegans embryogenesis, six rows of hypodermal cells adopt dorsal, lateral or ventral fates that go on to display distinct behaviors during larval life. Several transcription factors are known that function in specifying these major hypodermal cell fates, but our knowledge of the specification of these cell types is sparse, particularly in the case of the ventral hypodermal cells, which become Vulval Precursor Cells and form the vulval opening in response to extracellular signals. Previously, the gene pvl-4 was identified in a screen for mutants with defects in vulval development. We found by whole genome sequencing that pvl-4 is the Paired-box gene pax-3, which encodes the sole PAX-3 transcription factor homolog in C. elegans. pax-3 mutants show embryonic and larval lethality, and body morphology abnormalities indicative of hypodermal cell defects. We report that pax-3 is expressed in ventral P cells and their descendants during embryogenesis and early larval stages, and that in pax-3 reduction-of-function animals the ventral P cells undergo a cell fate transformation and express several markers of the lateral seam cell fate. Furthermore, forced expression of pax-3 in the lateral hypodermal cells causes them to lose expression of seam cell markers. We propose that pax-3 functions in the ventral hypodermal cells to prevent these cells from adopting the lateral seam cell fate. pax-3 represents the first gene required for specification solely of the ventral hypodermal fate in C. elegans providing insights into cell type diversification.
•A mutation affecting the C. elegans homolog of the transcription factor PAX3 was identified, and is identical to a human mutation associated with Waardenburg syndrome.•pax-3 reduction of function leads to ventral embryonic hypodermal cells adopting the fate of lateral embryonic hypodermal cell (lateral).•pax-3 is the first gene required for specification of the ventral hypodermal fate in the C. elegans embryo.•Unlike vertebrates or another nematode, P. pacificus, a role for pax-3 in myogenesis was not observed in this species. |
doi_str_mv | 10.1016/j.ydbio.2016.03.002 |
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•A mutation affecting the C. elegans homolog of the transcription factor PAX3 was identified, and is identical to a human mutation associated with Waardenburg syndrome.•pax-3 reduction of function leads to ventral embryonic hypodermal cells adopting the fate of lateral embryonic hypodermal cell (lateral).•pax-3 is the first gene required for specification of the ventral hypodermal fate in the C. elegans embryo.•Unlike vertebrates or another nematode, P. pacificus, a role for pax-3 in myogenesis was not observed in this species.</description><identifier>ISSN: 0012-1606</identifier><identifier>EISSN: 1095-564X</identifier><identifier>DOI: 10.1016/j.ydbio.2016.03.002</identifier><identifier>PMID: 26953187</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Animals, Genetically Modified ; C. elegans ; Caenorhabditis elegans - embryology ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans - metabolism ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Cell Lineage - genetics ; Differentiation ; Embryo, Nonmammalian - cytology ; Embryo, Nonmammalian - embryology ; Embryo, Nonmammalian - metabolism ; Epidermal Cells ; Epidermis ; Epidermis - embryology ; Epidermis - metabolism ; Fate specification ; Female ; Gene expression ; Larva - cytology ; Larva - genetics ; Larva - metabolism ; Luminescent Proteins - genetics ; Luminescent Proteins - metabolism ; Microscopy, Fluorescence ; Mutation ; Paired Box Transcription Factors - genetics ; Paired Box Transcription Factors - metabolism ; PAX ; RNA Interference ; Vulva - cytology ; Vulva - embryology ; Vulva - metabolism</subject><ispartof>Developmental biology, 2016-04, Vol.412 (2), p.191-207</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-538f3c8a7706e7c50a63b0926f5f0a46550673154bbd4f455f3074c73de80f2f3</citedby><cites>FETCH-LOGICAL-c525t-538f3c8a7706e7c50a63b0926f5f0a46550673154bbd4f455f3074c73de80f2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ydbio.2016.03.002$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26953187$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thompson, Kenneth W.</creatorcontrib><creatorcontrib>Joshi, Pradeep</creatorcontrib><creatorcontrib>Dymond, Jessica S.</creatorcontrib><creatorcontrib>Gorrepati, Lakshmi</creatorcontrib><creatorcontrib>Smith, Harold E.</creatorcontrib><creatorcontrib>Krause, Michael W.</creatorcontrib><creatorcontrib>Eisenmann, David M.</creatorcontrib><title>The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans</title><title>Developmental biology</title><addtitle>Dev Biol</addtitle><description>The development of the single cell layer skin or hypodermis of Caenorhabditis elegans is an excellent model for understanding cell fate specification and differentiation. Early in C. elegans embryogenesis, six rows of hypodermal cells adopt dorsal, lateral or ventral fates that go on to display distinct behaviors during larval life. Several transcription factors are known that function in specifying these major hypodermal cell fates, but our knowledge of the specification of these cell types is sparse, particularly in the case of the ventral hypodermal cells, which become Vulval Precursor Cells and form the vulval opening in response to extracellular signals. Previously, the gene pvl-4 was identified in a screen for mutants with defects in vulval development. We found by whole genome sequencing that pvl-4 is the Paired-box gene pax-3, which encodes the sole PAX-3 transcription factor homolog in C. elegans. pax-3 mutants show embryonic and larval lethality, and body morphology abnormalities indicative of hypodermal cell defects. We report that pax-3 is expressed in ventral P cells and their descendants during embryogenesis and early larval stages, and that in pax-3 reduction-of-function animals the ventral P cells undergo a cell fate transformation and express several markers of the lateral seam cell fate. Furthermore, forced expression of pax-3 in the lateral hypodermal cells causes them to lose expression of seam cell markers. We propose that pax-3 functions in the ventral hypodermal cells to prevent these cells from adopting the lateral seam cell fate. pax-3 represents the first gene required for specification solely of the ventral hypodermal fate in C. elegans providing insights into cell type diversification.
•A mutation affecting the C. elegans homolog of the transcription factor PAX3 was identified, and is identical to a human mutation associated with Waardenburg syndrome.•pax-3 reduction of function leads to ventral embryonic hypodermal cells adopting the fate of lateral embryonic hypodermal cell (lateral).•pax-3 is the first gene required for specification of the ventral hypodermal fate in the C. elegans embryo.•Unlike vertebrates or another nematode, P. pacificus, a role for pax-3 in myogenesis was not observed in this species.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>C. elegans</subject><subject>Caenorhabditis elegans - embryology</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - metabolism</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Cell Lineage - genetics</subject><subject>Differentiation</subject><subject>Embryo, Nonmammalian - cytology</subject><subject>Embryo, Nonmammalian - embryology</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Epidermal Cells</subject><subject>Epidermis</subject><subject>Epidermis - embryology</subject><subject>Epidermis - metabolism</subject><subject>Fate specification</subject><subject>Female</subject><subject>Gene expression</subject><subject>Larva - cytology</subject><subject>Larva - genetics</subject><subject>Larva - metabolism</subject><subject>Luminescent Proteins - genetics</subject><subject>Luminescent Proteins - metabolism</subject><subject>Microscopy, Fluorescence</subject><subject>Mutation</subject><subject>Paired Box Transcription Factors - genetics</subject><subject>Paired Box Transcription Factors - metabolism</subject><subject>PAX</subject><subject>RNA Interference</subject><subject>Vulva - cytology</subject><subject>Vulva - embryology</subject><subject>Vulva - metabolism</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhS0EotvCL0BCPnJJGMex4xxAqlZAkSrRQ5F6sxxnvOtVNg52dqH_HqdbKrhw8ljz3puxP0LeMCgZMPl-V973nQ9llS8l8BKgekZWDFpRCFnfPScrAFYVTII8I-cp7QCAK8VfkrNKtoIz1azIdLtFemN8xL7owi86xTCjH-nN5V3BacTNYTAzJjpnmd0Gb5F2OP9EHOnSiGagZuzpEcd5qXHyPcZ9riwOA3UP3hy3LikOuDFjekVeODMkfP14XpDvnz_drq-K629fvq4vrwsrKjEXgivHrTJNAxIbK8BI3kFbSSccmFoKAbLhTNRd19euFsJxaGrb8B4VuMrxC_LxlDsduj329rSgnqLfm3ivg_H6387ot3oTjrpWteRC5YB3jwEx_DhgmvXep-VVZsRwSJo1TatUVTVtlvKT1MaQUkT3NIaBXljpnX5gpRdWGrjOrLLr7d8bPnn-wMmCDycB5n86eow6WY-jxT7jsrPug__vgN-5jacc</recordid><startdate>20160415</startdate><enddate>20160415</enddate><creator>Thompson, Kenneth W.</creator><creator>Joshi, Pradeep</creator><creator>Dymond, Jessica S.</creator><creator>Gorrepati, Lakshmi</creator><creator>Smith, Harold E.</creator><creator>Krause, Michael W.</creator><creator>Eisenmann, David M.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160415</creationdate><title>The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans</title><author>Thompson, Kenneth W. ; Joshi, Pradeep ; Dymond, Jessica S. ; Gorrepati, Lakshmi ; Smith, Harold E. ; Krause, Michael W. ; Eisenmann, David M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-538f3c8a7706e7c50a63b0926f5f0a46550673154bbd4f455f3074c73de80f2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>C. elegans</topic><topic>Caenorhabditis elegans - embryology</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans - metabolism</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Cell Lineage - genetics</topic><topic>Differentiation</topic><topic>Embryo, Nonmammalian - cytology</topic><topic>Embryo, Nonmammalian - embryology</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Epidermal Cells</topic><topic>Epidermis</topic><topic>Epidermis - embryology</topic><topic>Epidermis - metabolism</topic><topic>Fate specification</topic><topic>Female</topic><topic>Gene expression</topic><topic>Larva - cytology</topic><topic>Larva - genetics</topic><topic>Larva - metabolism</topic><topic>Luminescent Proteins - genetics</topic><topic>Luminescent Proteins - metabolism</topic><topic>Microscopy, Fluorescence</topic><topic>Mutation</topic><topic>Paired Box Transcription Factors - genetics</topic><topic>Paired Box Transcription Factors - metabolism</topic><topic>PAX</topic><topic>RNA Interference</topic><topic>Vulva - cytology</topic><topic>Vulva - embryology</topic><topic>Vulva - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thompson, Kenneth W.</creatorcontrib><creatorcontrib>Joshi, Pradeep</creatorcontrib><creatorcontrib>Dymond, Jessica S.</creatorcontrib><creatorcontrib>Gorrepati, Lakshmi</creatorcontrib><creatorcontrib>Smith, Harold E.</creatorcontrib><creatorcontrib>Krause, Michael W.</creatorcontrib><creatorcontrib>Eisenmann, David M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thompson, Kenneth W.</au><au>Joshi, Pradeep</au><au>Dymond, Jessica S.</au><au>Gorrepati, Lakshmi</au><au>Smith, Harold E.</au><au>Krause, Michael W.</au><au>Eisenmann, David M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>2016-04-15</date><risdate>2016</risdate><volume>412</volume><issue>2</issue><spage>191</spage><epage>207</epage><pages>191-207</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><abstract>The development of the single cell layer skin or hypodermis of Caenorhabditis elegans is an excellent model for understanding cell fate specification and differentiation. Early in C. elegans embryogenesis, six rows of hypodermal cells adopt dorsal, lateral or ventral fates that go on to display distinct behaviors during larval life. Several transcription factors are known that function in specifying these major hypodermal cell fates, but our knowledge of the specification of these cell types is sparse, particularly in the case of the ventral hypodermal cells, which become Vulval Precursor Cells and form the vulval opening in response to extracellular signals. Previously, the gene pvl-4 was identified in a screen for mutants with defects in vulval development. We found by whole genome sequencing that pvl-4 is the Paired-box gene pax-3, which encodes the sole PAX-3 transcription factor homolog in C. elegans. pax-3 mutants show embryonic and larval lethality, and body morphology abnormalities indicative of hypodermal cell defects. We report that pax-3 is expressed in ventral P cells and their descendants during embryogenesis and early larval stages, and that in pax-3 reduction-of-function animals the ventral P cells undergo a cell fate transformation and express several markers of the lateral seam cell fate. Furthermore, forced expression of pax-3 in the lateral hypodermal cells causes them to lose expression of seam cell markers. We propose that pax-3 functions in the ventral hypodermal cells to prevent these cells from adopting the lateral seam cell fate. pax-3 represents the first gene required for specification solely of the ventral hypodermal fate in C. elegans providing insights into cell type diversification.
•A mutation affecting the C. elegans homolog of the transcription factor PAX3 was identified, and is identical to a human mutation associated with Waardenburg syndrome.•pax-3 reduction of function leads to ventral embryonic hypodermal cells adopting the fate of lateral embryonic hypodermal cell (lateral).•pax-3 is the first gene required for specification of the ventral hypodermal fate in the C. elegans embryo.•Unlike vertebrates or another nematode, P. pacificus, a role for pax-3 in myogenesis was not observed in this species.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26953187</pmid><doi>10.1016/j.ydbio.2016.03.002</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Genetically Modified C. elegans Caenorhabditis elegans - embryology Caenorhabditis elegans - genetics Caenorhabditis elegans - metabolism Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Cell Lineage - genetics Differentiation Embryo, Nonmammalian - cytology Embryo, Nonmammalian - embryology Embryo, Nonmammalian - metabolism Epidermal Cells Epidermis Epidermis - embryology Epidermis - metabolism Fate specification Female Gene expression Larva - cytology Larva - genetics Larva - metabolism Luminescent Proteins - genetics Luminescent Proteins - metabolism Microscopy, Fluorescence Mutation Paired Box Transcription Factors - genetics Paired Box Transcription Factors - metabolism PAX RNA Interference Vulva - cytology Vulva - embryology Vulva - metabolism |
title | The Paired-box protein PAX-3 regulates the choice between lateral and ventral epidermal cell fates in C. elegans |
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