Literature DB >> 12682014

FGFR1 is independently required in both developing mid- and hindbrain for sustained response to isthmic signals.

Ras Trokovic1, Nina Trokovic, Sanna Hernesniemi, Ulla Pirvola, Daniela M Vogt Weisenhorn, Janet Rossant, Andrew P McMahon, Wolfgang Wurst, Juha Partanen.   

Abstract

Fibroblast growth factors (FGFs) are signaling molecules of the isthmic organizer, which regulates development of the midbrain and cerebellum. Tissue-specific inactivation of one of the FGF receptor (FGFR) genes, Fgfr1, in the midbrain and rhombomere 1 of the hindbrain of mouse embryos results in deletion of the inferior colliculi in the posterior midbrain and vermis of the cerebellum. Analyses of both midbrain-hindbrain and midbrain-specific Fgfr1 mutants suggest that after establishment of the isthmic organizer, FGFR1 is needed for continued response to the isthmic signals, and that it has direct functions on both sides of the organizer. In addition, FGFR1 appears to modify cell adhesion properties critical for maintaining a coherent organizing center. This may be achieved by regulating expression of specific cell-adhesion molecules at the midbrain-hindbrain border.

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Year:  2003        PMID: 12682014      PMCID: PMC154461          DOI: 10.1093/emboj/cdg169

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  42 in total

1.  Expression of FGFR1, FGFR2 and FGFR3 during early neural development in the chick embryo.

Authors:  J Walshe; I Mason
Journal:  Mech Dev       Date:  2000-01       Impact factor: 1.882

Review 2.  Neural plate patterning: upstream and downstream of the isthmic organizer.

Authors:  W Wurst; L Bally-Cuif
Journal:  Nat Rev Neurosci       Date:  2001-02       Impact factor: 34.870

3.  Cell mixing between the embryonic midbrain and hindbrain.

Authors:  S Jungbluth; C Larsen; A Wizenmann; A Lumsden
Journal:  Curr Biol       Date:  2001-02-06       Impact factor: 10.834

4.  Two lineage boundaries coordinate vertebrate apical ectodermal ridge formation.

Authors:  R A Kimmel; D H Turnbull; V Blanquet; W Wurst; C A Loomis; A L Joyner
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

Review 5.  Turn-off, drop-out: functional state switching of cadherins.

Authors:  Jack Lilien; Janne Balsamo; Carlos Arregui; Gang Xu
Journal:  Dev Dyn       Date:  2002-05       Impact factor: 3.780

Review 6.  Early anterior/posterior patterning of the midbrain and cerebellum.

Authors:  A Liu; A L Joyner
Journal:  Annu Rev Neurosci       Date:  2001       Impact factor: 12.449

7.  FGF signaling regulates mesoderm cell fate specification and morphogenetic movement at the primitive streak.

Authors:  B Ciruna; J Rossant
Journal:  Dev Cell       Date:  2001-07       Impact factor: 12.270

8.  Comparison of the expression of three highly related genes, Fgf8, Fgf17 and Fgf18, in the mouse embryo.

Authors:  Y Maruoka; N Ohbayashi; M Hoshikawa; N Itoh; B L Hogan; Y Furuta
Journal:  Mech Dev       Date:  1998-06       Impact factor: 1.882

9.  Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression.

Authors:  C Irving; I Mason
Journal:  Development       Date:  2000-01       Impact factor: 6.868

10.  Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures.

Authors:  J Xu; Z Liu; D M Ornitz
Journal:  Development       Date:  2000-05       Impact factor: 6.868

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  83 in total

1.  Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning.

Authors:  Youngwook Ahn; Brian W Sanderson; Ophir D Klein; Robb Krumlauf
Journal:  Development       Date:  2010-08-19       Impact factor: 6.868

2.  Fetal and postnatal lung defects reveal a novel and required role for Fgf8 in lung development.

Authors:  Shibin Yu; Bryan Poe; Margaret Schwarz; Sarah A Elliot; Kurt H Albertine; Stephen Fenton; Vidu Garg; Anne M Moon
Journal:  Dev Biol       Date:  2010-08-19       Impact factor: 3.582

3.  Structural basis by which alternative splicing modulates the organizer activity of FGF8 in the brain.

Authors:  Shaun K Olsen; James Y H Li; Carrie Bromleigh; Anna V Eliseenkova; Omar A Ibrahimi; Zhimin Lao; Fuming Zhang; Robert J Linhardt; Alexandra L Joyner; Moosa Mohammadi
Journal:  Genes Dev       Date:  2005-12-29       Impact factor: 11.361

Review 4.  Genetic networks controlling the development of midbrain dopaminergic neurons.

Authors:  Nilima Prakash; Wolfgang Wurst
Journal:  J Physiol       Date:  2006-07-06       Impact factor: 5.182

Review 5.  An essential role for FGF receptor signaling in lens development.

Authors:  Michael L Robinson
Journal:  Semin Cell Dev Biol       Date:  2006-10-27       Impact factor: 7.727

6.  Fgfr1 is required for cortical regeneration and repair after perinatal hypoxia.

Authors:  Devon M Fagel; Yosif Ganat; Elise Cheng; John Silbereis; Yasushi Ohkubo; Laura R Ment; Flora M Vaccarino
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

7.  Neuron-derived FGF9 is essential for scaffold formation of Bergmann radial fibers and migration of granule neurons in the cerebellum.

Authors:  Yongshun Lin; Lijie Chen; Chunhong Lin; Yongde Luo; Robert Y L Tsai; Fen Wang
Journal:  Dev Biol       Date:  2009-02-20       Impact factor: 3.582

8.  Regulation of self-renewing neural progenitors by FGF/ERK signaling controls formation of the inferior colliculus.

Authors:  Alexander Dee; Kairong Li; Xin Heng; Qiuxia Guo; James Y H Li
Journal:  Development       Date:  2016-08-30       Impact factor: 6.868

9.  Fibroblast growth factor receptor signaling is essential for lens fiber cell differentiation.

Authors:  Haotian Zhao; Tianyu Yang; Bhavani P Madakashira; Cornelius A Thiels; Chad A Bechtle; Claudia M Garcia; Huiming Zhang; Kai Yu; David M Ornitz; David C Beebe; Michael L Robinson
Journal:  Dev Biol       Date:  2008-03-28       Impact factor: 3.582

10.  Misexpression of Gbx2 throughout the mesencephalon by a conditional gain-of-function transgene leads to deletion of the midbrain and cerebellum in mice.

Authors:  N Abimbola Sunmonu; Li Chen; James Y H Li
Journal:  Genesis       Date:  2009-10       Impact factor: 2.487

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