Literature DB >> 8187630

Postimplantation expression patterns indicate a role for the mouse forkhead/HNF-3 alpha, beta and gamma genes in determination of the definitive endoderm, chordamesoderm and neuroectoderm.

A P Monaghan1, K H Kaestner, E Grau, G Schütz.   

Abstract

The HNF-3 alpha, beta and gamma genes constitute a family of transcription factors that are required for hepatocyte-specific gene expression of a number of genes, e.g. transthyretin, alpha-1 antitrypsin and tyrosine aminotransferase. These genes share a highly conserved DNA-binding domain first found in the Drosophila gene, forkhead, which is required for the normal patterning of the developing gut and central nervous system in Drosophila. In adult mouse tissues, transcripts from HNF-3 alpha and beta have been localised to the liver, intestine and lung, whereas HNF-3 gamma is found in the liver, intestine and testis. In light of the early developmental significance of forkhead in Drosophila, we have compared the patterns of expression of HNF-3 alpha, beta and gamma mRNAs during murine embryogenesis. We find that these genes are sequentially activated during development in the definitive endoderm. HNF-3 beta mRNA is expressed in the node at the anterior end of the primitive streak in all three germ layers and is the first gene of this family to be activated. Subsequently, HNF-3 alpha is transcribed in the primitive endoderm in the region of the invaginating foregut and HNF-3 gamma appears upon hindgut differentiation. These genes have different anterior boundaries of mRNA expression in the developing endoderm and transcripts are found in all endoderm-derived structures that differentiate posterior to this boundary. Therefore, we propose that these genes define regionalization within the definitive endoderm. Furthermore, differential mRNA expression of HNF-3 alpha and beta is detected in cells of the ventral neural epithelium, chordamesoderm and notochord. In the neural epithelium, expression of HNF-3 alpha and beta mRNA becomes localised to cells of the floor plate. We propose that, in addition to their characterised requirement for liver-specific gene expression, HNF-3 alpha and beta are required for mesoderm and neural axis formation. We also conclude that HNF-3 beta is the true orthologue of the Drosophila forkhead gene.

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Year:  1993        PMID: 8187630     DOI: 10.1242/dev.119.3.567

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  145 in total

1.  Asymmetric and node-specific nodal expression patterns are controlled by two distinct cis-acting regulatory elements.

Authors:  D P Norris; E J Robertson
Journal:  Genes Dev       Date:  1999-06-15       Impact factor: 11.361

2.  FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse.

Authors:  P A Hoodless; M Pye; C Chazaud; E Labbé; L Attisano; J Rossant; J L Wrana
Journal:  Genes Dev       Date:  2001-05-15       Impact factor: 11.361

3.  Elevated levels of hepatocyte nuclear factor 3beta in mouse hepatocytes influence expression of genes involved in bile acid and glucose homeostasis.

Authors:  F M Rausa; Y Tan; H Zhou; K W Yoo; D B Stolz; S C Watkins; R R Franks; T G Unterman; R H Costa
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

4.  Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions.

Authors:  Shanru Li; Joel Weidenfeld; Edward E Morrisey
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

Review 5.  Regulation of gene expression in the intestinal epithelium.

Authors:  Camilla A Richmond; David T Breault
Journal:  Prog Mol Biol Transl Sci       Date:  2010       Impact factor: 3.622

6.  Atypical mouse cerebellar development is caused by ectopic expression of the forkhead box transcription factor HNF-3beta.

Authors:  H Zhou; D E Hughes; M L Major; K Yoo; C Pesold; R H Costa
Journal:  Gene Expr       Date:  2001

7.  Hypoblast controls mesoderm generation and axial patterning in the gastrulating rabbit embryo.

Authors:  Jan Idkowiak; Gunnar Weisheit; Juliane Plitzner; Christoph Viebahn
Journal:  Dev Genes Evol       Date:  2004-10-06       Impact factor: 0.900

8.  Essential function of PTP-PEST during mouse embryonic vascularization, mesenchyme formation, neurogenesis and early liver development.

Authors:  Jacinthe Sirois; Jean-François Côté; Alain Charest; Noriko Uetani; Annie Bourdeau; Stephen A Duncan; Eugene Daniels; Michel L Tremblay
Journal:  Mech Dev       Date:  2006-09-01       Impact factor: 1.882

9.  Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells.

Authors:  Paul Gadue; Tara L Huber; Patrick J Paddison; Gordon M Keller
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-31       Impact factor: 11.205

10.  Nato3 integrates with the Shh-Foxa2 transcriptional network regulating the differentiation of midbrain dopaminergic neurons.

Authors:  Einat Nissim-Eliraz; Sophie Zisman; Omri Schatz; Nissim Ben-Arie
Journal:  J Mol Neurosci       Date:  2012-12-21       Impact factor: 3.444

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