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Development, Vol 118, Issue 1 47-59, Copyright © 1993 by Company of Biologists
JOURNAL ARTICLES |
H Sasaki and BL Hogan
Department of Cell Biology, Vanderbilt University Medical School, Nashville, Tennessee 37232.
Four genes encoding fork-head-domain-containing proteins (FD genes) have been isolated from a mouse 8.5 days post coitum (p.c.) embryo cDNA library. Two are mouse homologues of rat HNF-3 beta and HNF-3 alpha. The other two are novel and have been named MF-1 and MF-2 (for mesoderm/mesenchyme fork head). Wholemount in situ hybridization of embryos between 6.5 and 9.5 days p. c. shows that each gene has a unique expression pattern. HNF-3 beta is expressed in the node, notochord, floor plate and gut, while HNF-3 alpha is mainly in the definitive endoderm and gut, but also in the floor plate of the midbrain. These results suggest that HNF-3 beta and HNF-3 alpha, in addition to their known functions as transcriptional activators in adult liver, play a role in body axis formation, neural tube patterning and definitive endoderm formation during gastrulation. MF-1 RNA is present in non-notochordal mesoderm, and in neural-crest-derived head mesenchyme, while MF-2 transcripts are found in the sclerotomes of the somites and in head mesenchyme, including that from neural crest. Studies on gastrulation stage embryos suggest that the early temporal and spatial patterns of HNF-3 beta, MF-1 and HNF-3 alpha correlate with populations of cells undergoing commitment to different developmental fates. A model is proposed linking FD gene expression with gastrulation events in the mouse.
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C Faust, K. Lawson, N. Schork, B Thiel, and T Magnuson The Polycomb-group gene eed is required for normal morphogenetic movements during gastrulation in the mouse embryo Development, January 11, 1998; 125(22): 4495 - 4506. [Abstract] [PDF] |
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M. Matise, D. Epstein, H. Park, K. Platt, and A. Joyner Gli2 is required for induction of floor plate and adjacent cells, but not most ventral neurons in the mouse central nervous system Development, January 8, 1998; 125(15): 2759 - 2770. [Abstract] [PDF] |
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D. Roberts, D. Smith, D. Goff, and C. Tabin Epithelial-mesenchymal signaling during the regionalization of the chick gut Development, January 8, 1998; 125(15): 2791 - 2801. [Abstract] [PDF] |
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D Dufort, L Schwartz, K Harpal, and J Rossant The transcription factor HNF3beta is required in visceral endoderm for normal primitive streak morphogenesis Development, January 8, 1998; 125(16): 3015 - 3025. [Abstract] [PDF] |
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P. Thomas, A Brown, and R. Beddington Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors Development, January 1, 1998; 125(1): 85 - 94. [Abstract] [PDF] |
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D. G. Overdier, H. Ye, R. S. Peterson, D. E. Clevidence, and R. H. Costa The Winged Helix Transcriptional Activator HFH-3 Is Expressed in the Distal Tubules of Embryonic and Adult Mouse Kidney J. Biol. Chem., May 23, 1997; 272(21): 13725 - 13730. [Abstract] [Full Text] [PDF] |
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A I McClatchey, I Saotome, V Ramesh, J F Gusella, and T Jacks The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation. Genes & Dev., May 15, 1997; 11(10): 1253 - 1265. [Abstract] [PDF] |
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J D Molkentin, Q Lin, S A Duncan, and E N Olson Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis. Genes & Dev., April 15, 1997; 11(8): 1061 - 1072. [Abstract] [PDF] |
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L. Lim, H. Zhou, and R. H. Costa The winged helix transcription factor HFH-4 is expressed during choroid plexus epithelial development in the mouse embryo PNAS, April 1, 1997; 94(7): 3094 - 3099. [Abstract] [Full Text] [PDF] |
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G E Winnier, L Hargett, and B L Hogan The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo. Genes & Dev., April 1, 1997; 11(7): 926 - 940. [Abstract] [PDF] |
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R Wehr, A Mansouri, T de Maeyer, and P Gruss Fkh5-deficient mice show dysgenesis in the caudal midbrain and hypothalamic mammillary body Development, January 11, 1997; 124(22): 4447 - 4456. [Abstract] [PDF] |
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K Iida, H Koseki, H Kakinuma, N Kato, Y Mizutani-Koseki, H Ohuchi, H Yoshioka, S Noji, K Kawamura, Y Kataoka, et al. Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis Development, January 11, 1997; 124(22): 4627 - 4638. [Abstract] [PDF] |
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Y Takihara, D Tomotsune, M Shirai, Y Katoh-Fukui, K Nishii, M. Motaleb, M Nomura, R Tsuchiya, Y Fujita, Y Shibata, et al. Targeted disruption of the mouse homologue of the Drosophila polyhomeotic gene leads to altered anteroposterior patterning and neural crest defects Development, January 10, 1997; 124(19): 3673 - 3682. [Abstract] [PDF] |
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S Qu, K. Niswender, Q Ji, R van der Meer, D Keeney, M. Magnuson, and R Wisdom Polydactyly and ectopic ZPA formation in Alx-4 mutant mice Development, January 10, 1997; 124(20): 3999 - 4008. [Abstract] [PDF] |
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C. Olsen and W. Jeffery A forkhead gene related to HNF-3beta is required for gastrulation and axis formation in the ascidian embryo Development, January 9, 1997; 124(18): 3609 - 3619. [Abstract] [PDF] |
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