Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7270
pubmed:dateCreated
2009-11-12
pubmed:databankReference
pubmed:abstractText
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.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-10433909, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-10581021, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-1090005, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-11586359, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-11951044, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-12192408, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-12524352, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-12599277, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-14557539, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-15192806, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-15620360, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-15877281, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-15983371, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-16211615, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-16272123, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-16909383, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17033973, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17082449, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17327847, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17623668, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17999357, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-17999362, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-18551524, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-18849986, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-19107409, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-19477152, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-19490899, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-19907485, http://linkedlifedata.com/resource/pubmed/commentcorrection/19907493-9582070
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1476-4687
pubmed:author
pubmed:issnType
Electronic
pubmed:day
12
pubmed:volume
462
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
213-7
pubmed:dateRevised
2010-12-17
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Human-specific transcriptional regulation of CNS development genes by FOXP2.
pubmed:affiliation
Program in Neurogenetics, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA. gena@alum.mit.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural