Literature DB >> 18079162

The medaka FoxP2, a homologue of human language gene FOXP2, has a diverged structure and function.

Tatsuo Itakura1, Abhishek Chandra, Zhi Yang, Xiaodong Xue, Bo Wang, Wataru Kimura, Keisuke Hikosaka, Keiji Inohaya, Akira Kudo, Tadayoshi Uezato, Naoyuki Miura.   

Abstract

Forkhead box (Fox) genes are involved in organogenesis and cell differentiation. A mutation of FOXP2 was discovered in patients with severe defects in speech and language. The medaka FoxP2 was cloned in order to clarify the molecular evolution and difference in the protein structure and function by comparing human/mouse and medaka genes. The result showed that medaka FoxP2 had a 73.7% homology to the human and mouse counterparts, and its zinc finger, leucine zipper and forkhead domain structures were conserved. However, medaka FoxP2 lacked a long polyglutamine repeat and had two insertions of unique amino acid sequences. FoxP2 expression was found in the epiphysis and retina, in addition to the midbrain and cerebellum. The transcriptional assay revealed that medaka FoxP2 showed a very weak repressive activity to the CC10 promoter while mouse Foxp2 exhibited a strong repressive activity. Mutational analyses of medaka FoxP2 showed that the three amino acids of forkhead domain were responsible for the weak repressive activity. These results suggest that medaka FoxP2 may play a different function in the development of the medaka fish.

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Year:  2007        PMID: 18079162     DOI: 10.1093/jb/mvm235

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  5 in total

Review 1.  Human brain evolution: from gene discovery to phenotype discovery.

Authors:  Todd M Preuss
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-20       Impact factor: 11.205

Review 2.  Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language.

Authors:  Constance Scharff; Jana Petri
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-07-27       Impact factor: 6.237

3.  Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

Authors:  Sara B Estruch; Sarah A Graham; Swathi M Chinnappa; Pelagia Deriziotis; Simon E Fisher
Journal:  J Neurodev Disord       Date:  2016-11-28       Impact factor: 4.025

4.  Domain-specific regulation of foxP2 CNS expression by lef1.

Authors:  Joshua L Bonkowsky; Xu Wang; Esther Fujimoto; Ji Eun Lee; Chi-Bin Chien; Richard I Dorsky
Journal:  BMC Dev Biol       Date:  2008-10-24       Impact factor: 1.978

5.  Rapid diversification of FoxP2 in teleosts through gene duplication in the teleost-specific whole genome duplication event.

Authors:  Xiaowei Song; Yajun Wang; Yezhong Tang
Journal:  PLoS One       Date:  2013-12-09       Impact factor: 3.240

  5 in total

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