Publication Date:
2009-11-13
Description:
The signalling pathways controlling both the evolution and development of language in the human brain remain unknown. So far, the transcription factor FOXP2 (forkhead box P2) is the only gene implicated in Mendelian forms of human speech and language dysfunction. It has been proposed that the amino acid composition in the human variant of FOXP2 has undergone accelerated evolution, and this two-amino-acid change occurred around the time of language emergence in humans. However, this remains controversial, and whether the acquisition of these amino acids in human FOXP2 has any functional consequence in human neurons remains untested. Here we demonstrate that these two human-specific amino acids alter FOXP2 function by conferring differential transcriptional regulation in vitro. We extend these observations in vivo to human and chimpanzee brain, and use network analysis to identify novel relationships among the differentially expressed genes. These data provide experimental support for the functional relevance of changes in FOXP2 that occur on the human lineage, highlighting specific pathways with direct consequences for human brain development and disease in the central nervous system (CNS). Because FOXP2 has an important role in speech and language in humans, the identified targets may have a critical function in the development and evolution of language circuitry in humans.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778075/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778075/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Konopka, Genevieve -- Bomar, Jamee M -- Winden, Kellen -- Coppola, Giovanni -- Jonsson, Zophonias O -- Gao, Fuying -- Peng, Sophia -- Preuss, Todd M -- Wohlschlegel, James A -- Geschwind, Daniel H -- N01-HD-4-3368/HD/NICHD NIH HHS/ -- N01-HD-4-3383/HD/NICHD NIH HHS/ -- R21 MH075028/MH/NIMH NIH HHS/ -- R21 MH075028-02/MH/NIMH NIH HHS/ -- R21MH075028/MH/NIMH NIH HHS/ -- R37 MH060233/MH/NIMH NIH HHS/ -- R37 MH060233-06A1/MH/NIMH NIH HHS/ -- R37MH60233-06A1/MH/NIMH NIH HHS/ -- RR00165/RR/NCRR NIH HHS/ -- T32HD007032/HD/NICHD NIH HHS/ -- T32MH073526/MH/NIMH NIH HHS/ -- England -- Nature. 2009 Nov 12;462(7270):213-7. doi: 10.1038/nature08549.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Neurogenetics, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA. gena@alum.mit.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19907493" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Brain/cytology/*embryology/*metabolism
;
Cell Line
;
Evolution, Molecular
;
Forkhead Transcription Factors/chemistry/genetics/*metabolism
;
*Gene Expression Regulation, Developmental
;
Humans
;
Language
;
Pan troglodytes/embryology/genetics/metabolism
;
Promoter Regions, Genetic/genetics
;
Species Specificity
;
Speech/physiology
;
*Transcription, Genetic
;
Transcriptional Activation
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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