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http://purl.uniprot.org/citations/19386265http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19386265http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19386265http://www.w3.org/2000/01/rdf-schema#comment"How asymmetric divisions are connected to the terminal differentiation program of neuronal subtypes is poorly understood. In C. elegans, two homeodomain transcription factors, TTX-3 (a LHX2/9 ortholog) and CEH-10 (a CHX10 ortholog), directly activate a large battery of terminal differentiation genes in the cholinergic interneuron AIY. We establish here a transcriptional cascade linking asymmetric division to this differentiation program. A transient lineage-specific input formed by the Zic factor REF-2 and the bHLH factor HLH-2 directly activates ttx-3 expression in the AIY mother. During the terminal division of the AIY mother, an asymmetric Wnt/beta-catenin pathway cooperates with TTX-3 to directly restrict ceh-10 expression to only one of the two daughter cells. TTX-3 and CEH-10 automaintain their expression, thereby locking in the differentiation state. Our study establishes how transient lineage and asymmetric division inputs are integrated and suggests that the Wnt/beta-catenin pathway is widely used to control the identity of neuronal lineages."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.org/dc/terms/identifier"doi:10.1016/j.devcel.2009.02.011"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.org/dc/terms/identifier"doi:10.1016/j.devcel.2009.02.011"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/author"Hobert O."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/author"Hobert O."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/author"Bertrand V."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/author"Bertrand V."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/name"Dev. Cell"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/name"Dev. Cell"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/pages"563-575"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/pages"563-575"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/title"Linking asymmetric cell division to the terminal differentiation program of postmitotic neurons in C. elegans."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/title"Linking asymmetric cell division to the terminal differentiation program of postmitotic neurons in C. elegans."xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/19386265http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/19386265http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19386265
http://purl.uniprot.org/citations/19386265http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19386265
http://purl.uniprot.org/citations/19386265http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19386265
http://purl.uniprot.org/citations/19386265http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19386265
http://purl.uniprot.org/uniprot/G5EE86http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/19386265
http://purl.uniprot.org/uniprot/Q10666http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/19386265