Journal Article PreJuSER-10473

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On the genetic architecture of coritcal folding and brain volume in primates

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2010
Academic Press Orlando, Fla.

NeuroImage 53, 1103 - 1108 () [10.1016/j.neuroimage.2010.02.020]

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Abstract: Understanding the evolutionary forces that produced the human brain is a central problem in neuroscience and human biology. Comparisons across primate species show that both brain volume and gyrification (the degree of folding in the cerebral cortex) have progressively increased during primate evolution and there is a strong positive correlation between these two traits across primate species. The human brain is exceptional among primates in both total volume and gyrification, and therefore understanding the genetic mechanisms influencing variation in these traits will improve our understanding of a landmark feature of our species. Here we show that individual variation in gyrification is significantly heritable in both humans and an Old World monkey (baboons, Papio hamadryas). Furthermore, contrary to expectations based on the positive phenotypic correlation across species, the genetic correlation between cerebral volume and gyrification within both humans and baboons is estimated as negative. These results suggest that the positive relationship between cerebral volume and cortical folding across species cannot be explained by one set of selective pressures or genetic changes. Our data suggest that one set of selective pressures favored the progressive increase in brain volume documented in the primate fossil record, and that a second independent selective process, possibly related to parturition and neonatal brain size, may have favored brains with progressively greater cortical folding. Without a second separate selective pressure, natural selection favoring increased brain volume would be expected to produce less folded, more lissencephalic brains. These results provide initial evidence for the heritability of gyrification, and possibly a new perspective on the evolutionary mechanisms underlying long-term changes in the nonhuman primate and human brain.

Keyword(s): Animals (MeSH) ; Biological Evolution (MeSH) ; Cerebral Cortex: anatomy & histology (MeSH) ; Female (MeSH) ; Humans (MeSH) ; Image Processing, Computer-Assisted (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Male (MeSH) ; Papio: anatomy & histology (MeSH) ; Primates: anatomy & histology (MeSH) ; Species Specificity (MeSH) ; J


Note: This work was supported in part by grants from the US National Institute of Mental Health (MH078111, MH059490, and MH078143), the National Institute of Biomedical Imaging and Bioengineering (K01 EB006395) and the National Center for Research Resources base grant to the Southwest National Primate Research Center (P51-RR013986). We are grateful to the participants in the Genetics of Brain Structure Study. The supercomputing facilities used for this work at the AT&T Genetics Computing Center were supported in part by a gift from the AT&T Foundation. The work was carried out in facilities that were constructed with support from Research Facilities Improvement grants C06-RR013556, C06-RR015456 and C06-RR014578 from the National Center for Research Resources, NIH. We also wish to thank two anonymous reviewers for their helpful recommendations.

Contributing Institute(s):
  1. Molekulare Organisation des Gehirns (INM-2)
  2. Jülich-Aachen Research Alliance - Translational Brain Medicine (JARA-BRAIN)
Research Program(s):
  1. Funktion und Dysfunktion des Nervensystems (FUEK409) (FUEK409)
  2. 89571 - Connectivity and Activity (POF2-89571) (POF2-89571)

Appears in the scientific report 2010
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 Record created 2012-11-13, last modified 2021-01-29


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