Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7028
pubmed:dateCreated
2005-2-24
pubmed:abstractText
Most stem cells are not totipotent. Instead, they are partially committed but remain undifferentiated. Upon appropriate stimulation they are capable of regenerating mature cell types. Little is known about the genetic programmes that maintain the undifferentiated phenotype of lineage-restricted stem cells. Here we describe the molecular details of a nodal point in adult melanocyte stem cell differentiation in which Pax3 simultaneously functions to initiate a melanogenic cascade while acting downstream to prevent terminal differentiation. Pax3 activates expression of Mitf, a transcription factor critical for melanogenesis, while at the same time it competes with Mitf for occupancy of an enhancer required for expression of dopachrome tautomerase, an enzyme that functions in melanin synthesis. Pax3-expressing melanoblasts are thus committed but undifferentiated until Pax3-mediated repression is relieved by activated beta-catenin. Thus, a stem cell transcription factor can both determine cell fate and simultaneously maintain an undifferentiated state, leaving a cell poised to differentiate in response to external stimuli.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CTNNB1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Catnb protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intramolecular Oxidoreductases, http://linkedlifedata.com/resource/pubmed/chemical/MITF protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Microphthalmia-Associated..., http://linkedlifedata.com/resource/pubmed/chemical/Mitf protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Paired Box Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Pax3 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/beta Catenin, http://linkedlifedata.com/resource/pubmed/chemical/dopachrome isomerase
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1476-4687
pubmed:author
pubmed:issnType
Electronic
pubmed:day
24
pubmed:volume
433
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
884-7
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15729346-Aging, pubmed-meshheading:15729346-Animals, pubmed-meshheading:15729346-Base Sequence, pubmed-meshheading:15729346-Binding, Competitive, pubmed-meshheading:15729346-Cell Differentiation, pubmed-meshheading:15729346-Cell Line, pubmed-meshheading:15729346-Cell Lineage, pubmed-meshheading:15729346-Cytoskeletal Proteins, pubmed-meshheading:15729346-DNA-Binding Proteins, pubmed-meshheading:15729346-Enhancer Elements, Genetic, pubmed-meshheading:15729346-Gene Expression Regulation, pubmed-meshheading:15729346-Hair Follicle, pubmed-meshheading:15729346-Humans, pubmed-meshheading:15729346-Intramolecular Oxidoreductases, pubmed-meshheading:15729346-Melanocytes, pubmed-meshheading:15729346-Mice, pubmed-meshheading:15729346-Microphthalmia-Associated Transcription Factor, pubmed-meshheading:15729346-Molecular Sequence Data, pubmed-meshheading:15729346-Paired Box Transcription Factors, pubmed-meshheading:15729346-Sequence Deletion, pubmed-meshheading:15729346-Stem Cells, pubmed-meshheading:15729346-Trans-Activators, pubmed-meshheading:15729346-Transcription Factors, pubmed-meshheading:15729346-beta Catenin
pubmed:year
2005
pubmed:articleTitle
Pax3 functions at a nodal point in melanocyte stem cell differentiation.
pubmed:affiliation
Cardiovascular Division, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.