Format

Send to

Choose Destination
See comment in PubMed Commons below
Nat Commun. 2012;3:1079. doi: 10.1038/ncomms2086.

Genetic architecture supports mosaic brain evolution and independent brain-body size regulation.

Author information

1
Computational and Evolutionary Biology Group, Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester M13 9PT, UK.
2
Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
3
Jiangsu Key Laboratory of Neuroregeneration, Nantong University, China.
4
Department of Neurology, Beth Isreal Deaconess Medical Center, 330 Brookline Ave., Boston, MA 02215, USA.
#
Contributed equally

Abstract

The mammalian brain consists of distinct parts that fulfil different functions. Finlay and Darlington have argued that evolution of the mammalian brain is constrained by developmental programs, suggesting that different brain parts are not free to respond individually to selection and evolve independent of other parts or overall brain size. However, comparisons among mammals with matched brain weights often reveal greater differences in brain part size, arguing against strong developmental constraints. Here we test these hypotheses using a quantitative genetic approach involving over 10,000 mice. We identify independent loci for size variation in seven key parts of the brain, and observe that brain parts show low or no phenotypic correlation, as is predicted by a mosaic scenario. We also demonstrate that variation in brain size is independently regulated from body size. The allometric relations seen at higher phylogenetic levels are thus unlikely to be the product of strong developmental constraints.

PMID:
23011133
PMCID:
PMC4267555
DOI:
10.1038/ncomms2086
[Indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Nature Publishing Group Icon for PubMed Central
    Loading ...
    Support Center