Adaptive evolution of ASPM, a major determinant of cerebral cortical size in humans.

A prominent trend in the evolution of humans is the progressive enlargement of the cerebral cortex. The ASPM (Abnormal spindle-like microcephaly associated) gene has the potential to play a role in this evolutionary process, because mutations in this gene cause severe reductions in the cerebral cortical size of affected humans. Here, we show that the evolution of ASPM is significantly accelerated in great apes, especially along the ape lineages leading to humans. Additionally, the lineage from the last human/chimpanzee ancestor to humans shows an excess of non-synonymous over synonymous substitutions, which is a signature of positive Darwinian selection. A comparison of polymorphism and divergence using the McDonald-Kreitman test confirms that ASPM has indeed experienced intense positive selection during recent human evolution. This test also reveals that, on average, ASPM fixed one advantageous amino acid change in every 300,000-400,000 years since the human lineage diverged from chimpanzees some 5-6 million years ago. We therefore conclude that ASPM underwent strong adaptive evolution in the descent of Homo sapiens, which is consistent with its putative role in the evolutionary enlargement of the human brain.

[1]  B. Finlay,et al.  Linked regularities in the development and evolution of mammalian brains. , 1995, Science.

[2]  D. Glover,et al.  Polo kinase and Asp are needed to promote the mitotic organizing activity of centrosomes , 2001, Nature Cell Biology.

[3]  J. Fryns,et al.  Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32. , 2000, American journal of human genetics.

[4]  M. Abramowicz,et al.  Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15. , 1999, American journal of human genetics.

[5]  D. Labie,et al.  Molecular Evolution , 1991, Nature.

[6]  B. Bainbridge,et al.  Genetics , 1981, Experientia.

[7]  R. Saunders,et al.  The Drosophila Gene abnormal spindle Encodes a Novel Microtubule-associated Protein That Associates with the Polar Regions of the Mitotic Spindle , 1997, The Journal of cell biology.

[8]  Justin C. Fay,et al.  Positive and negative selection on the human genome. , 2001, Genetics.

[9]  C. Woods,et al.  Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter. , 1998, American journal of human genetics.

[10]  C. Noback,et al.  The primate brain , 1970 .

[11]  Wen-Hsiung Li Unbiased estimation of the rates of synonymous and nonsynonymous substitution , 2006, Journal of Molecular Evolution.

[12]  Alexander F. Markham,et al.  ASPM is a major determinant of cerebral cortical size , 2002, Nature Genetics.

[13]  C. Woods,et al.  The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2 , 1999, European Journal of Human Genetics.

[14]  M. Kreitman,et al.  Adaptive protein evolution at the Adh locus in Drosophila , 1991, Nature.

[15]  M. Kreitman,et al.  Methods to detect selection in populations with applications to the human. , 2000, Annual review of genomics and human genetics.

[16]  Christopher A. Walsh,et al.  Molecular genetics of human microcephaly , 2001, Current opinion in neurology.

[17]  Justin C. Fay,et al.  Testing the neutral theory of molecular evolution with genomic data from Drosophila , 2002, Nature.

[18]  Jerel Clayton Davis,et al.  Molecular evolution meets the genomics revolution , 2005 .

[19]  S. O’Brien,et al.  Molecular phylogenetics and the origins of placental mammals , 2001, Nature.

[20]  C. Woods,et al.  A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31. , 2000, American journal of human genetics.

[21]  W. Dobyns Primary microcephaly: new approaches for an old disorder. , 2002, American journal of medical genetics.

[22]  P. Rakic A small step for the cell, a giant leap for mankind: a hypothesis of neocortical expansion during evolution , 1995, Trends in Neurosciences.

[23]  V. Caviness,et al.  Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model , 1995, Trends in Neurosciences.

[24]  C. Woods,et al.  A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34. , 2000, American journal of human genetics.

[25]  Santiago F. Elena,et al.  A Sliding Window-Based Method to Detect Selective Constraints in Protein-Coding Genes and Its Application to RNA Viruses , 2002, Journal of Molecular Evolution.

[26]  J. Ávila,et al.  A cell division mutant of drosophila with a functionally abnormal spindle , 1985, Cell.

[27]  C. Groves,et al.  Toward a phylogenetic classification of Primates based on DNA evidence complemented by fossil evidence. , 1998, Molecular phylogenetics and evolution.

[28]  C. Walsh,et al.  Protein-truncating mutations in ASPM cause variable reduction in brain size. , 2003, American journal of human genetics.

[29]  Gerald J. Wyckoff,et al.  Rapid evolution of male reproductive genes in the descent of man , 2000, Nature.