Literature DB >> 8162862

Distinct developmental expression of a new avian fibroblast growth factor receptor.

C Marcelle1, A Eichmann, O Halevy, C Bréant, N M Le Douarin.   

Abstract

We have cloned a new member of the fibroblast growth factor receptor family from avian embryonic RNA. The FREK (for fibroblast growth factor receptor-like embryonic kinase) primary transcript can be alternatively spliced in a tissue- and stage-specific manner to give rise to molecules containing either two or three Ig-like domains. During elongating primitive streak stages, FREK is expressed in the rostral and lateral epiblast and in the Hensen's node. From 2.5 days of development (E 2.5) on, it is expressed in various ectoderm- and mesoderm-derived structures. Most striking is FREK expression in the skeletal muscle lineage. It is highly expressed in the early myotome and, at later stages, in all skeletal muscles of the embryo. From E9 to hatching, FREK expression in the muscles decreases dramatically but is maintained in satellite cells of adult muscles. FREK transcript is elevated upon addition of basic fibroblast growth factor to serum-starved satellite cells. From this study, we conclude: (1) that the structure and pattern of expression of FREK set it apart from other cloned fibroblast growth factor receptors (FGFR) and suggest that FREK is a new member of that family; (2) that FREK may play multiple roles in early avian development, including a specialized role in the early differentiation of skeletal muscle.

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Year:  1994        PMID: 8162862     DOI: 10.1242/dev.120.3.683

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


  8 in total

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Review 2.  Embryonic angiogenesis: a review.

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Journal:  Naturwissenschaften       Date:  1996-04

3.  Hic1 Defines Quiescent Mesenchymal Progenitor Subpopulations with Distinct Functions and Fates in Skeletal Muscle Regeneration.

Authors:  R Wilder Scott; Martin Arostegui; Ronen Schweitzer; Fabio M V Rossi; T Michael Underhill
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4.  Genomic structure and complete sequence of the human FGFR4 gene.

Authors:  M Kostrzewa; U Müller
Journal:  Mamm Genome       Date:  1998-02       Impact factor: 2.957

5.  Activation of Pax3 target genes is necessary but not sufficient for neurogenesis in the ophthalmic trigeminal placode.

Authors:  Carolynn M Dude; C-Y Kelly Kuan; James R Bradshaw; Nicholas D E Greene; Frédéric Relaix; Michael R Stark; Clare V H Baker
Journal:  Dev Biol       Date:  2008-12-07       Impact factor: 3.582

6.  FGF signaling is essential for ophthalmic trigeminal placode cell delamination and differentiation.

Authors:  Rhonda N T Lassiter; Stephanie B Reynolds; Kristopher D Marin; Tyler F Mayo; Michael R Stark
Journal:  Dev Dyn       Date:  2009-05       Impact factor: 3.780

7.  Pax3 isoforms in sensory neurogenesis: expression and function in the ophthalmic trigeminal placode.

Authors:  Jason S Adams; Sterling N Sudweeks; Michael R Stark
Journal:  Dev Dyn       Date:  2014-01-28       Impact factor: 3.780

8.  FGFR1 inhibits skeletal muscle atrophy associated with hindlimb suspension.

Authors:  John Eash; Aaron Olsen; Gert Breur; Dave Gerrard; Kevin Hannon
Journal:  BMC Musculoskelet Disord       Date:  2007-04-10       Impact factor: 2.362

  8 in total

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