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dc.contributor.authorKarp, Xantha
dc.contributor.authorAmbros, Victor R.
dc.date2022-08-11T08:10:18.000
dc.date.accessioned2022-08-23T17:03:30Z
dc.date.available2022-08-23T17:03:30Z
dc.date.issued2011-01-01
dc.date.submitted2015-01-12
dc.identifier.citation<p>Genetics. 2011 Jan;187(1):345-53. doi: 10.1534/genetics.110.123992. Epub 2010 Oct 26. <a href="http://dx.doi.org/10.1534/genetics.110.123992" target="_blank">Link to article on publisher's site</a></p>
dc.identifier.issn0016-6731 (Linking)
dc.identifier.doi10.1534/genetics.110.123992
dc.identifier.pmid20980238
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44438
dc.description.abstractAnimals developing in the wild encounter a range of environmental conditions, and so developmental mechanisms have evolved that can accommodate different environmental contingencies. Harsh environmental conditions cause Caenorhabditis elegans larvae to arrest as stress-resistant "dauer" larvae after the second larval stage (L2), thereby indefinitely postponing L3 cell fates. HBL-1 is a key transcriptional regulator of L2 vs. L3 cell fate. Through the analysis of genetic interactions between mutations of hbl-1 and of genes encoding regulators of dauer larva formation, we find that hbl-1 can also modulate the dauer formation decision in a complex manner. We propose that dynamic interactions between genes that regulate stage-specific cell fate decisions and those that regulate dauer formation promote the robustness of developmental outcomes to changing environmental conditions.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20980238&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018311/
dc.subjectAnimals
dc.subjectCaenorhabditis elegans
dc.subjectCaenorhabditis elegans Proteins
dc.subjectCytochrome P-450 Enzyme System
dc.subjectDNA-Binding Proteins
dc.subjectInsulin
dc.subjectLarva
dc.subjectSignal Transduction
dc.subjectTime Factors
dc.subjectTranscription Factors
dc.subjectTransforming Growth Factor beta
dc.subjectBiochemistry
dc.subjectDevelopmental Biology
dc.subjectMolecular Biology
dc.subjectMolecular Genetics
dc.titleThe developmental timing regulator HBL-1 modulates the dauer formation decision in Caenorhabditis elegans
dc.typeJournal Article
dc.source.journaltitleGenetics
dc.source.volume187
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pmm_pp/30
dc.identifier.contextkey6519782
html.description.abstract<p>Animals developing in the wild encounter a range of environmental conditions, and so developmental mechanisms have evolved that can accommodate different environmental contingencies. Harsh environmental conditions cause Caenorhabditis elegans larvae to arrest as stress-resistant "dauer" larvae after the second larval stage (L2), thereby indefinitely postponing L3 cell fates. HBL-1 is a key transcriptional regulator of L2 vs. L3 cell fate. Through the analysis of genetic interactions between mutations of hbl-1 and of genes encoding regulators of dauer larva formation, we find that hbl-1 can also modulate the dauer formation decision in a complex manner. We propose that dynamic interactions between genes that regulate stage-specific cell fate decisions and those that regulate dauer formation promote the robustness of developmental outcomes to changing environmental conditions.</p>
dc.identifier.submissionpathpmm_pp/30
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages345-53


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