Literature DB >> 7789270

Multiple roles for FGF-3 during cranial neural development in the chicken.

R Mahmood1, P Kiefer, S Guthrie, C Dickson, I Mason.   

Abstract

FGF-3 has been implicated in the development of the hindbrain and otocyst in vertebrate embryos. Since the chicken embryo offers a favourable system in which to study the development of these structures, we have isolated and characterised cDNAs for chicken Fgf-3 and determined its pattern of expression in chick embryos from stage 3 (primitive streak) to stage 25 (early organogenesis). Within the developing cranial neural tube, Fgf-3 exhibits dynamic spatial and temporal expression. During extension of the head process, RNA is detected in the midline of the developing neural plate. In neurulating embryos, transcripts are observed initially in rhombomeres 4 and 5 of the hindbrain and later, in rhombomere 6. During hindbrain development, expression is lost from these rhombomeres, but becomes restricted to rhombomere boundaries, providing an intracellular marker which distinguishes a population of cells within boundary regions. Fgf-3 expression is elevated in ventral and medial boundary regions and is greatly reduced in dorsal parts. Studies of regenerating rhombomere boundaries show that Fgf-3 expression is induced in reforming boundaries when even-numbered rhombomere tissue is grafted next to odd, but not when like is juxtaposed to like. Fgf-3 disappears from boundary regions just prior to the loss of the morphological boundaries suggesting a boundary-associated function. Other sites of expression have also been identified. At early stages of development Fgf-3 is expressed in the epiblast and mesendoderm of the primitive streak, in mesoderm lateral to the streak and in Hensen's node. In older embryos transcripts are detected in the endoderm of the pharyngeal pouches, the ectoderm of the second and third pharyngeal arches and the stomodeum. Expression was also detected in the segmental plate and in the posterior half of the three most-recently generated somites.

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Year:  1995        PMID: 7789270     DOI: 10.1242/dev.121.5.1399

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


  25 in total

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2.  GATA-4 interacts distinctively with negative and positive regulatory elements in the Fgf-3 promoter.

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Journal:  Nucleic Acids Res       Date:  2002-02-15       Impact factor: 16.971

3.  Ring1A is a transcriptional repressor that interacts with the Polycomb-M33 protein and is expressed at rhombomere boundaries in the mouse hindbrain.

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Review 4.  Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

Authors:  C Kappen; A Neubüser; R Balling; R Finnell
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2007-12

5.  Restricted expression of the actin-regulatory protein, tropomyosin, defines distinct boundaries, evaginating neuroepithelium, and choroid plexus forerunners during early CNS development.

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Journal:  J Neurosci       Date:  1996-11-01       Impact factor: 6.167

6.  Hoxb-2 transcriptional activation in rhombomeres 3 and 5 requires an evolutionarily conserved cis-acting element in addition to the Krox-20 binding site.

Authors:  C Vesque; M Maconochie; S Nonchev; L Ariza-McNaughton; A Kuroiwa; P Charnay; R Krumlauf
Journal:  EMBO J       Date:  1996-10-01       Impact factor: 11.598

7.  Expression of Fgf-3 in relation to hindbrain segmentation, otic pit position and pharyngeal arch morphology in normal and retinoic acid-exposed mouse embryos.

Authors:  R Mahmood; I J Mason; G M Morriss-Kay
Journal:  Anat Embryol (Berl)       Date:  1996-07

Review 8.  SOX7: from a developmental regulator to an emerging tumor suppressor.

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Journal:  Histol Histopathol       Date:  2013-11-29       Impact factor: 2.303

9.  FGF8 initiates inner ear induction in chick and mouse.

Authors:  Raj K Ladher; Tracy J Wright; Anne M Moon; Suzanne L Mansour; Gary C Schoenwolf
Journal:  Genes Dev       Date:  2005-03-01       Impact factor: 11.361

10.  FGF signaling controls caudal hindbrain specification through Ras-ERK1/2 pathway.

Authors:  Ferran Aragon; Cristina Pujades
Journal:  BMC Dev Biol       Date:  2009-12-03       Impact factor: 1.978

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