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Heterozygous PAX6 mutation, adult brain structure and fronto‐striato‐thalamic function in a human family
Author(s) -
EllisonWright Zoë,
Heyman Isobel,
Frampton Ian,
Rubia Katya,
Chitnis Xavier,
EllisonWright Ian,
Williams Steve C. R.,
Suckling John,
Simmons Andrew,
Bullmore Edward
Publication year - 2004
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2004.03236.x
Subject(s) - neuroscience , pax6 , forebrain , corpus callosum , psychology , splenium , thalamus , neurocognitive , white matter , schizophrenia (object oriented programming) , biology , cognition , magnetic resonance imaging , central nervous system , genetics , medicine , gene , radiology , psychiatry , transcription factor
Recent progress in developmental neurobiology and neuroimaging can be drawn together to provide new insight into the links between genetically specified processes of embryonic brain development and adult human brain structure and function. We used magnetic resonance imaging (MRI) to show that individuals with aniridia and deficits in executive and social cognition, due to heterozygous mutation of the neurodevelopmental control gene PAX6 , have structural abnormalities of grey matter in anterior cingulate cortex, cerebellum and medial temporal lobe, as well as white matter deficits in corpus callosum. Functional MRI demonstrated reduced activation of fronto‐striato‐thalamic systems during performance of overt verbal fluency and nonsense sentence completion; the most consistent abnormality of verbal executive activation was located in the thalamus. These results provide the first evidence for brain functional differences in humans with PAX6 mutation that are compatible both with anatomical abnormalities in the same subjects and, more circumstantially, with the known roles of murine Pax6 in regional differentiation, axonal guidance and other aspects of early forebrain development. Highly conserved homeobox genes may be critical for normal ontogenesis of large‐scale neurocognitive networks supporting phylogenetically advanced mental functions.