RRC ID 6387
著者 King RS, Maiden SL, Hawkins NC, Kidd AR 3rd, Kimble J, Hardin J, Walston TD.
タイトル The N- or C-terminal domains of DSH-2 can activate the C. elegans Wnt/beta-catenin asymmetry pathway.
ジャーナル Dev Biol
Abstract Dishevelleds are modular proteins that lie at the crossroads of divergent Wnt signaling pathways. The DIX domain of dishevelleds modulates a beta-catenin destruction complex, and thereby mediates cell fate decisions through differential activation of Tcf transcription factors. The DEP domain of dishevelleds mediates planar polarity of cells within a sheet through regulation of actin modulators. In Caenorhabditis elegans asymmetric cell fate decisions are regulated by asymmetric localization of signaling components in a pathway termed the Wnt/beta-catenin asymmetry pathway. Which domain(s) of Disheveled regulate this pathway is unknown. We show that C. elegans embryos from dsh-2(or302) mutant mothers fail to successfully undergo morphogenesis, but transgenes containing either the DIX or the DEP domain of DSH-2 are sufficient to rescue the mutant phenotype. Embryos lacking zygotic function of SYS-1/beta-catenin, WRM-1/beta-catenin, or POP-1/Tcf show defects similar to dsh-2 mutants, including a loss of asymmetry in some cell fate decisions. Removal of two dishevelleds (dsh-2 and mig-5) leads to a global loss of POP-1 asymmetry, which can be rescued by addition of transgenes containing either the DIX or DEP domain of DSH-2. These results indicate that either the DIX or DEP domain of DSH-2 is capable of activating the Wnt/beta-catenin asymmetry pathway and regulating anterior-posterior fate decisions required for proper morphogenesis.
巻・号 328(2)
ページ 234-44
公開日 2009-4-15
DOI 10.1016/j.ydbio.2009.01.017
PII S0012-1606(09)00054-2
PMID 19298786
PMC PMC4409331
MeSH Animals Animals, Genetically Modified Body Patterning / physiology Caenorhabditis elegans / cytology Caenorhabditis elegans / embryology Caenorhabditis elegans / physiology* Caenorhabditis elegans Proteins / genetics Caenorhabditis elegans Proteins / physiology* Cell Cycle Proteins / genetics Cell Cycle Proteins / physiology* Cell Polarity / physiology Cytoskeletal Proteins / physiology* DNA-Binding Proteins / physiology Dishevelled Proteins Embryo, Nonmammalian / physiology High Mobility Group Proteins / physiology Mutation Protein Structure, Tertiary Signal Transduction / physiology Transcription Factors / physiology* Wnt Proteins / physiology* beta Catenin / physiology*
IF 2.896
引用数 17
WOS 分野 DEVELOPMENTAL BIOLOGY
リソース情報
線虫 tm2133