Literature DB >> 27878434

Regional selection of the brain size regulating gene CASC5 provides new insight into human brain evolution.

Lei Shi1, Enzhi Hu1,2, Zhenbo Wang3, Jiewei Liu1,2, Jin Li4, Ming Li1,5, Hua Chen6, Chunshui Yu7, Tianzi Jiang3,8,9,10, Bing Su11.   

Abstract

Human evolution is marked by a continued enlargement of the brain. Previous studies on human brain evolution focused on identifying sequence divergences of brain size regulating genes between humans and nonhuman primates. However, the evolutionary pattern of the brain size regulating genes during recent human evolution is largely unknown. We conducted a comprehensive analysis of the brain size regulating gene CASC5 and found that in recent human evolution, CASC5 has accumulated many modern human specific amino acid changes, including two fixed changes and six polymorphic changes. Among human populations, 4 of the 6 amino acid polymorphic sites have high frequencies of derived alleles in East Asians, but are rare in Europeans and Africans. We proved that this between-population allelic divergence was caused by regional Darwinian positive selection in East Asians. Further analysis of brain image data of Han Chinese showed significant associations of the amino acid polymorphic sites with gray matter volume. Hence, CASC5 may contribute to the morphological and structural changes of the human brain during recent evolution. The observed between-population divergence of CASC5 variants was driven by natural selection that tends to favor a larger gray matter volume in East Asians.

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Year:  2016        PMID: 27878434     DOI: 10.1007/s00439-016-1748-5

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  52 in total

1.  A codon-based model of nucleotide substitution for protein-coding DNA sequences.

Authors:  N Goldman; Z Yang
Journal:  Mol Biol Evol       Date:  1994-09       Impact factor: 16.240

2.  Mitochondrial DNA and human evolution.

Authors:  R L Cann; M Stoneking; A C Wilson
Journal:  Nature       Date:  1987 Jan 1-7       Impact factor: 49.962

3.  Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.

Authors:  Timothy W Yu; Ganeshwaran H Mochida; David J Tischfield; Sema K Sgaier; Laura Flores-Sarnat; Consolato M Sergi; Meral Topçu; Marie T McDonald; Brenda J Barry; Jillian M Felie; Christine Sunu; William B Dobyns; Rebecca D Folkerth; A James Barkovich; Christopher A Walsh
Journal:  Nat Genet       Date:  2010-10-03       Impact factor: 38.330

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

Authors:  Patrick D Evans; Jeffrey R Anderson; Eric J Vallender; Sandra L Gilbert; Christine M Malcom; Steve Dorus; Bruce T Lahn
Journal:  Hum Mol Genet       Date:  2004-01-13       Impact factor: 6.150

5.  Kinetochore KMN network gene CASC5 mutated in primary microcephaly.

Authors:  Anne Genin; Julie Desir; Nelle Lambert; Martine Biervliet; Nathalie Van Der Aa; Genevieve Pierquin; Audrey Killian; Mario Tosi; Montse Urbina; Anne Lefort; Frederick Libert; Isabelle Pirson; Marc Abramowicz
Journal:  Hum Mol Genet       Date:  2012-09-13       Impact factor: 6.150

6.  ASPM is a major determinant of cerebral cortical size.

Authors:  Jacquelyn Bond; Emma Roberts; Ganesh H Mochida; Daniel J Hampshire; Sheila Scott; Jonathan M Askham; Kelly Springell; Meera Mahadevan; Yanick J Crow; Alexander F Markham; Christopher A Walsh; C Geoffrey Woods
Journal:  Nat Genet       Date:  2002-09-23       Impact factor: 38.330

7.  Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion.

Authors:  Natalay Kouprina; Adam Pavlicek; Ganeshwaran H Mochida; Gregory Solomon; William Gersch; Young-Ho Yoon; Randall Collura; Maryellen Ruvolo; J Carl Barrett; C Geoffrey Woods; Christopher A Walsh; Jerzy Jurka; Vladimir Larionov
Journal:  PLoS Biol       Date:  2004-03-23       Impact factor: 8.029

8.  The complete genome sequence of a Neanderthal from the Altai Mountains.

Authors:  Kay Prüfer; Fernando Racimo; Nick Patterson; Flora Jay; Sriram Sankararaman; Susanna Sawyer; Anja Heinze; Gabriel Renaud; Peter H Sudmant; Cesare de Filippo; Heng Li; Swapan Mallick; Michael Dannemann; Qiaomei Fu; Martin Kircher; Martin Kuhlwilm; Michael Lachmann; Matthias Meyer; Matthias Ongyerth; Michael Siebauer; Christoph Theunert; Arti Tandon; Priya Moorjani; Joseph Pickrell; James C Mullikin; Samuel H Vohr; Richard E Green; Ines Hellmann; Philip L F Johnson; Hélène Blanche; Howard Cann; Jacob O Kitzman; Jay Shendure; Evan E Eichler; Ed S Lein; Trygve E Bakken; Liubov V Golovanova; Vladimir B Doronichev; Michael V Shunkov; Anatoli P Derevianko; Bence Viola; Montgomery Slatkin; David Reich; Janet Kelso; Svante Pääbo
Journal:  Nature       Date:  2013-12-18       Impact factor: 49.962

9.  An integrated map of genetic variation from 1,092 human genomes.

Authors:  Goncalo R Abecasis; Adam Auton; Lisa D Brooks; Mark A DePristo; Richard M Durbin; Robert E Handsaker; Hyun Min Kang; Gabor T Marth; Gil A McVean
Journal:  Nature       Date:  2012-11-01       Impact factor: 49.962

10.  Interactions of genetic variants reveal inverse modulation patterns of dopamine system on brain gray matter volume and resting-state functional connectivity in healthy young adults.

Authors:  Jiayuan Xu; Wen Qin; Bing Liu; Tianzi Jiang; Chunshui Yu
Journal:  Brain Struct Funct       Date:  2015-10-25       Impact factor: 3.270

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  3 in total

1.  Parallel pathways for recruiting effector proteins determine centromere drive and suppression.

Authors:  Tomohiro Kumon; Jun Ma; R Brian Akins; Derek Stefanik; C Erik Nordgren; Junhyong Kim; Mia T Levine; Michael A Lampson
Journal:  Cell       Date:  2021-08-24       Impact factor: 66.850

Review 2.  Evolution of eukaryotic centromeres by drive and suppression of selfish genetic elements.

Authors:  Tomohiro Kumon; Michael A Lampson
Journal:  Semin Cell Dev Biol       Date:  2022-03-26       Impact factor: 7.499

3.  Microcephaly Modeling of Kinetochore Mutation Reveals a Brain-Specific Phenotype.

Authors:  Attya Omer Javed; Yun Li; Julien Muffat; Kuan-Chung Su; Malkiel A Cohen; Tenzin Lungjangwa; Patrick Aubourg; Iain M Cheeseman; Rudolf Jaenisch
Journal:  Cell Rep       Date:  2018-10-09       Impact factor: 9.423

  3 in total

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