| Literature DB >> 24769279 |
Masaki Kato1, Kazuo Okanoya2, Taku Koike3, Erika Sasaki4, Hideyuki Okano5, Shigeru Watanabe6, Atsushi Iriki7.
Abstract
Language is a characteristic feature of human communication. Several familial language impairments have been identified, and candidate genes for language impairments already isolated. Studies comparing expression patterns of these genes in human brain are necessary to further understanding of these genes. However, it is difficult to examine gene expression in human brain. In this study, we used a non-human primate (common marmoset; Callithrix jacchus) as a biological model of the human brain to investigate expression patterns of human speech- and reading-related genes. Expression patterns of speech disorder- (FoxP2, FoxP1, CNTNAP2, and CMIP) and dyslexia- (ROBO1, DCDC2, and KIAA0319) related genes were analyzed. We found the genes displayed overlapping expression patterns in the ocular, auditory, and motor systems. Our results enhance understanding of the molecular mechanisms underlying language impairments.Entities:
Keywords: Common marmoset; Dyslexia; Gene expression; Language; Specific language impairment; Vocal communication
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Year: 2014 PMID: 24769279 DOI: 10.1016/j.bandl.2014.03.007
Source DB: PubMed Journal: Brain Lang ISSN: 0093-934X Impact factor: 2.381