Literature DB >> 8155584

Sequential expression of HNF-3 beta and HNF-3 alpha by embryonic organizing centers: the dorsal lip/node, notochord and floor plate.

A Ruiz i Altaba1, V R Prezioso, J E Darnell, T M Jessell.   

Abstract

Axial patterning in the nervous system of vertebrate embryos depends on inductive signals that derive from the organizer region (the dorsal lip in amphibians and the node in birds and mammals) and leter from the notochord and floor plate. Previous studies have shown that Pintallavis, a member of the HNF-3/fork head transcription factor family, is expressed selectively by these cell groups in frog embryos and may be involved in regulating neural development. We report here that in early rat and mouse embryos, the embryonic endoderm, the node, the notochord and the floor plate express two related transcription factors, HNF-3 alpha and HNF-3 beta, which also function in the control of liver cell differentiation. Early embryonic tissues express variant forms of HNF-3 beta which derive from the use of 5' alternative exons. Within the organizer region and notochord, HNF-3 beta and HNF-3 alpha have distinct temporal patterns of expression and appear in partially overlapping domains. The early expression pattern of mammalian HNF-3 beta in the node, notochord and midline neural plate cells is similar to that of Pintallavis in frog embryos. There does not appear to be a Pintallavis homologue in mice. This prompted us to isolate and analyze the expression of the frog HNF-3 beta gene. In frog embryos, HNF-3 beta is expressed in the dorsal lip, pharyngeal endoderm and floor plate. In contrast to mammalian HNF-3 beta, the onset of frog HNF-3 beta expression in neural tissue occurs after neural tube closure. Thus, the combined expression patterns of Pintallavis and HNF-3 beta in frogs is equivalent to that of HNF-3 beta in rats and mice. Within neural tissue, the onset of expression of these regulatory genes define successive stages in the differentiation of floor plate cells. The results reported here show that closely related members of the HNF-3/fork head gene family are expressed by axial midline cell groups involved in neural induction and patterning and suggest the involvement of these genes in the development of the vertebrate neuraxis.

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Year:  1993        PMID: 8155584     DOI: 10.1016/0925-4773(93)90060-b

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  39 in total

1.  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

2.  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

3.  A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling.

Authors:  Sara M Peyrot; John B Wallingford; Richard M Harland
Journal:  Dev Biol       Date:  2011-01-27       Impact factor: 3.582

4.  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

5.  Homeoprotein hhex-induced conversion of intestinal to ventral pancreatic precursors results in the formation of giant pancreata in Xenopus embryos.

Authors:  Hui Zhao; Dandan Han; Igor B Dawid; Tomas Pieler; Yonglong Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-16       Impact factor: 11.205

6.  Persistent dopamine functions of neurons derived from embryonic stem cells in a rodent model of Parkinson disease.

Authors:  Jose A Rodríguez-Gómez; Jian-Qiang Lu; Iván Velasco; Seth Rivera; Sami S Zoghbi; Jeih-San Liow; John L Musachio; Frederick T Chin; Hiroshi Toyama; Jurgen Seidel; Michael V Green; Panayotis K Thanos; Masanori Ichise; Victor W Pike; Robert B Innis; Ron D G McKay
Journal:  Stem Cells       Date:  2006-12-14       Impact factor: 6.277

7.  Hepatocyte nuclear factor 3/fork head homolog 11 is expressed in proliferating epithelial and mesenchymal cells of embryonic and adult tissues.

Authors:  H Ye; T F Kelly; U Samadani; L Lim; S Rubio; D G Overdier; K A Roebuck; R H Costa
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

Review 8.  Making sense out of spinal cord somatosensory development.

Authors:  Helen C Lai; Rebecca P Seal; Jane E Johnson
Journal:  Development       Date:  2016-10-01       Impact factor: 6.868

9.  Identification of a transthyretin enhancer site that selectively binds the hepatocyte nuclear factor-3 beta isoform.

Authors:  U Samadani; X Qian; R H Costa
Journal:  Gene Expr       Date:  1996

10.  Role of Foxa-2 in adipocyte metabolism and differentiation.

Authors:  Christian Wolfrum; David Q Shih; Satoru Kuwajima; Andrew W Norris; C Ronald Kahn; Markus Stoffel
Journal:  J Clin Invest       Date:  2003-07-15       Impact factor: 14.808

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