Literature DB >> 19846726

The development of the thalamic motor learning area is regulated by Fgf8 expression.

Almudena Martinez-Ferre1, Salvador Martinez.   

Abstract

Habenular nuclei play a key role in the control of motor and cognitive behavior, processing emotion, motivation, and reward values in the brain. Thus, analysis of the molecular and cellular mechanisms underlying the development and evolution of this region will contribute to a better understanding of brain function. The Fgf8 gene is expressed in the dorsal midline of the diencephalon, close to the area in which the habenular region will develop. Given that Fgf8 is an important morphogenetic signal, we decided to investigate the role of Fgf8 signaling in diencephalic development. To this end, we analyzed the effects of altered Fgf8 expression in the mouse embryo, using molecular and cellular markers. Decreasing Fgf8 activity in the diencephalon was found to be associated with dosage-dependent alterations in the epithalamus: the habenular region and pineal gland are reduced or lacking in Fgf8 hypomorphic mice. Actually, our findings indicate that Fgf8 may be the master gene for these diencephalic domains, acting as an inductive and morphogenetic regulator. Therefore, the emergence of the habenular region in vertebrates could be understood in terms of a phylogenetic territorial addition caused by de novo expression of Fgf8 in the diencephalic alar plate. This region specializes to permit the development of adaptive control of the motor function in the vertebrate brain.

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Year:  2009        PMID: 19846726      PMCID: PMC6665203          DOI: 10.1523/JNEUROSCI.2625-09.2009

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  23 in total

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Authors:  Qiuxia Guo; James Y H Li
Journal:  Development       Date:  2019-04-01       Impact factor: 6.868

2.  Gbx2 is essential for maintaining thalamic neuron identity and repressing habenular characters in the developing thalamus.

Authors:  Chatterjee Mallika; Qiuxia Guo; James Y H Li
Journal:  Dev Biol       Date:  2015-08-20       Impact factor: 3.582

3.  Fractone-associated N-sulfated heparan sulfate shows reduced quantity in BTBR T+tf/J mice: a strong model of autism.

Authors:  Ksenia Z Meyza; D Caroline Blanchard; Brandon L Pearson; Roger L H Pobbe; Robert J Blanchard
Journal:  Behav Brain Res       Date:  2011-11-12       Impact factor: 3.332

4.  BTBR T+tf/J mice: autism-relevant behaviors and reduced fractone-associated heparan sulfate.

Authors:  D Caroline Blanchard; Erwin B Defensor; Ksenia Z Meyza; Roger L H Pobbe; Brandon L Pearson; Valerie J Bolivar; Robert J Blanchard
Journal:  Neurosci Biobehav Rev       Date:  2011-07-01       Impact factor: 8.989

Review 5.  Numerous isoforms of Fgf8 reflect its multiple roles in the developing brain.

Authors:  N Abimbola Sunmonu; Kairong Li; James Y H Li
Journal:  J Cell Physiol       Date:  2011-07       Impact factor: 6.384

6.  Fgf signaling governs cell fate in the zebrafish pineal complex.

Authors:  Joshua A Clanton; Kyle D Hope; Joshua T Gamse
Journal:  Development       Date:  2013-01-15       Impact factor: 6.868

Review 7.  Building a bridal chamber: development of the thalamus.

Authors:  Steffen Scholpp; Andrew Lumsden
Journal:  Trends Neurosci       Date:  2010-06-11       Impact factor: 13.837

Review 8.  Development and connectivity of the habenular nuclei.

Authors:  Sara Roberson; Marnie E Halpern
Journal:  Semin Cell Dev Biol       Date:  2017-11-06       Impact factor: 7.727

9.  Regulation of thalamic development by sonic hedgehog.

Authors:  Douglas J Epstein
Journal:  Front Neurosci       Date:  2012-04-18       Impact factor: 4.677

10.  A SINE-derived element constitutes a unique modular enhancer for mammalian diencephalic Fgf8.

Authors:  Akiko Nakanishi; Naoki Kobayashi; Asuka Suzuki-Hirano; Hidenori Nishihara; Takeshi Sasaki; Mika Hirakawa; Kenta Sumiyama; Tomomi Shimogori; Norihiro Okada
Journal:  PLoS One       Date:  2012-08-24       Impact factor: 3.240

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