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dc.contributor.authorHart, Daniel O.
dc.contributor.authorRaha, Tamal
dc.contributor.authorLawson, Nathan D.
dc.contributor.authorGreen, Michael R.
dc.date2022-08-11T08:09:32.000
dc.date.accessioned2022-08-23T16:35:02Z
dc.date.available2022-08-23T16:35:02Z
dc.date.issued2007-11-30
dc.date.submitted2009-03-16
dc.identifier.citation<p>Nature. 2007 Dec 13;450(7172):1082-5. Epub 2007 Nov 28. <a href="http://dx.doi.org/10.1038/nature06349">Link to article on publisher's site</a></p>
dc.identifier.issn1476-4687 (Electronic)
dc.identifier.doi10.1038/nature06349
dc.identifier.pmid18046332
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38468
dc.description.abstractTATA-box-binding protein (TBP)-related factor 3, TRF3 (also called TBP2), is a vertebrate-specific member of the TBP family that has a conserved carboxy-terminal region and DNA-binding domain virtually identical to that of TBP (ref. 1). TRF3 is highly expressed during embryonic development, and studies in zebrafish and Xenopus have shown that it is required for normal embryogenesis. Here we show that zebrafish embryos depleted of Trf3 exhibit multiple developmental defects and, in particular, fail to undergo haematopoiesis. Expression profiling for Trf3-dependent genes identified mespa, which encodes a transcription factor whose murine orthologue is required for mesoderm specification, and chromatin immunoprecipitation verified that Trf3 binds to the mespa promoter. Depletion of Mespa resulted in developmental and haematopoietic defects markedly similar to those induced by Trf3 depletion. Injection of mespa messenger RNA (mRNA) restored normal development to a Trf3-depleted embryo, indicating mespa is the single Trf3 target gene required for zebrafish embryogenesis. Zebrafish embryos depleted of Trf3 or Mespa also failed to express cdx4, a caudal-related gene required for haematopoiesis. Mespa binds to the cdx4 promoter, and epistasis analysis revealed an ordered trf3-mespa-cdx4 pathway. Thus, in zebrafish, commitment of mesoderm to the haematopoietic lineage occurs through a transcription factor pathway initiated by a TBP-related factor.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18046332&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150749/
dc.subjectAnimals
dc.subjectBasic Helix-Loop-Helix Transcription
dc.subjectFactors
dc.subjectEmbryonic Development
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation, Developmental
dc.subject*Hematopoiesis
dc.subjectHomeodomain Proteins
dc.subjectMice
dc.subjectTATA Box Binding Protein-Like Proteins
dc.subjectZebrafish
dc.subjectZebrafish Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleInitiation of zebrafish haematopoiesis by the TATA-box-binding protein-related factor Trf3
dc.typeJournal Article
dc.source.journaltitleNature
dc.source.volume450
dc.source.issue7172
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1338
dc.identifier.contextkey783015
html.description.abstract<p>TATA-box-binding protein (TBP)-related factor 3, TRF3 (also called TBP2), is a vertebrate-specific member of the TBP family that has a conserved carboxy-terminal region and DNA-binding domain virtually identical to that of TBP (ref. 1). TRF3 is highly expressed during embryonic development, and studies in zebrafish and Xenopus have shown that it is required for normal embryogenesis. Here we show that zebrafish embryos depleted of Trf3 exhibit multiple developmental defects and, in particular, fail to undergo haematopoiesis. Expression profiling for Trf3-dependent genes identified mespa, which encodes a transcription factor whose murine orthologue is required for mesoderm specification, and chromatin immunoprecipitation verified that Trf3 binds to the mespa promoter. Depletion of Mespa resulted in developmental and haematopoietic defects markedly similar to those induced by Trf3 depletion. Injection of mespa messenger RNA (mRNA) restored normal development to a Trf3-depleted embryo, indicating mespa is the single Trf3 target gene required for zebrafish embryogenesis. Zebrafish embryos depleted of Trf3 or Mespa also failed to express cdx4, a caudal-related gene required for haematopoiesis. Mespa binds to the cdx4 promoter, and epistasis analysis revealed an ordered trf3-mespa-cdx4 pathway. Thus, in zebrafish, commitment of mesoderm to the haematopoietic lineage occurs through a transcription factor pathway initiated by a TBP-related factor.</p>
dc.identifier.submissionpathoapubs/1338
dc.contributor.departmentProgram in Gene Function and Expression Program in Gene Function and Expression
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages1082-5


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