Revision as of 08:35, 19 June 2010 editCitation bot 1 (talk | contribs)Bots130,044 editsm Citations: added: issue, pmc, last2, first2, last3, first3, last4, first4, last5, first5, last6, first6. Tweaked: pmid, year. You can use this bot yourself! Report bugs here.← Previous edit | Revision as of 08:51, 19 August 2010 edit undoRjwilmsiBot (talk | contribs)Bots, Pending changes reviewers1,602,950 editsm →Controversy: CiteCompletion, {{dead link}}s: 1 using AWB (7016)Next edit → | ||
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}}</ref> ], writing in The ], wrote that as a result of the findings, "our cherished national dream of a well-mixed and harmonious meritocracy may be unattainable."<ref>{{cite |
}}</ref> ], writing in The ], wrote that as a result of the findings, "our cherished national dream of a well-mixed and harmonious meritocracy may be unattainable."<ref>{{cite news | ||
|url=http://findarticles.com/p/articles/mi_m1282/is_20_57/ai_n15895156/pg_3?tag=artBody;col1 | |url=http://findarticles.com/p/articles/mi_m1282/is_20_57/ai_n15895156/pg_3?tag=artBody;col1 | ||
|title=The specter of difference | |title=The specter of difference | ||
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Lahn's study began to attract considerable controversy in the science world. ] considers the two published papers as "egregious examples of going well beyond the data to try to make a splash." Lahn maintains that the science of his studies are sound, and freely admits that a direct link between these particular genes and either cognition or intelligence has not yet been conclusively established. Bruce Lahn is now engaging himself with other areas of study.<ref></ref><ref>{{cite journal | Lahn's study began to attract considerable controversy in the science world. ] considers the two published papers as "egregious examples of going well beyond the data to try to make a splash." Lahn maintains that the science of his studies are sound, and freely admits that a direct link between these particular genes and either cognition or intelligence has not yet been conclusively established. Bruce Lahn is now engaging himself with other areas of study.<ref></ref><ref>{{cite journal |
Revision as of 08:51, 19 August 2010
microcephaly, primary autosomal recessive 1 | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Symbol | MCPH1 | ||||||
Alt. symbols | Microcephalin, BRIT1 | ||||||
NCBI gene | 79648 | ||||||
HGNC | 6954 | ||||||
OMIM | 607117 | ||||||
UniProt | Q8NEM0 | ||||||
Other data | |||||||
Locus | Chr. 8 p23 | ||||||
|
microcephaly, primary autosomal recessive 2 | |
---|---|
Identifiers | |
Symbol | MCPH2 |
NCBI gene | 4181 |
HGNC | 6955 |
OMIM | 604317 |
Other data | |
Locus | Chr. 19 q13.1-13.2 |
microcephaly, primary autosomal recessive 3 | |
---|---|
Identifiers | |
Symbol | CDK5RAP2 |
Alt. symbols | MCPH3 |
NCBI gene | 23702 |
HGNC | 6956 |
OMIM | 604804 |
Other data | |
Locus | Chr. 9 q33.3 |
microcephaly, primary autosomal recessive 4 | |
---|---|
Identifiers | |
Symbol | MCPH4 |
NCBI gene | 23701 |
HGNC | 6957 |
OMIM | 604321 |
Other data | |
Locus | Chr. 15 q15-21 |
microcephaly, primary autosomal recessive 5 | |
---|---|
Identifiers | |
Symbol | ASPM |
Alt. symbols | MCPH5 |
NCBI gene | 64590 |
HGNC | 6958 |
OMIM | 608716 |
Other data | |
Locus | Chr. 1 q31 |
microcephaly, primary autosomal recessive 6 | |
---|---|
Identifiers | |
Symbol | CENPJ |
Alt. symbols | MCPH6 |
NCBI gene | 170629 |
HGNC | 17120 |
OMIM | 608393 |
Other data | |
Locus | Chr. 13 q12.2 |
Microcephalin (MCPH1) is one of six genes causing primary microcephaly (Online Mendelian Inheritance in Man (OMIM): 251200) when non-functional mutations exist in the homozygous state. Derived from the Greek words for "small" and "head", this condition is characterised by a severely diminished brain. Hence it has been assumed that variants have a role in brain development, but in normal individuals no effect on mental ability, brain size or behavior has been attributed to either this or another similarly studied microcephaly gene, ASPM.
Expression in the brain
MCPH1 is expressed in the fetal brain, in the developing forebrain, and on the walls of the lateral ventricles. Cells of this area divide, producing neurons that migrate to eventually form the cerebral cortex.
Evolution
A derived form of MCPH1 called haplogroup D appeared about 37,000 years ago (anytime between 14,000 and 60,000 years ago) and has spread to become the more common form throughout the world except Sub-Saharan Africa. The timing of its emergence may have closely preceded the Upper Paleolithic, when people started colonising Europe, although the margin of error is substantial and there is evidence that the transition to the Upper Paleolithic occurred in Africa before spreading to Europe. Doubts concerning origins aside, modern distributions of chromosomes bearing the ancestral forms of MCPH1 and MCPH5 coincide with the incidence of tonal languages, although the nature of this relationship can only be guessed at.
Haplogroup D may have originated from a lineage separated from modern humans approximately 1.1 million years ago and later introgressed into humans. This finding supports the possibility of admixture between modern humans and extinct Homo spp. While Neanderthals were suggested to be the possible source of this haplotype, it was not found in the individuals used to prepare the first draft of the Neanderthal genome.
On the other hand the sample of 89 individuals with only nine Africans used in the study has been criticized as being inadequate for the conclusion the paper draws, and comparable studies demonstrate that undersampling specific areas of East/Central Africa may lead to unwarranted conclusions. Additionally, scientists have not identified the evolutionary pressures that caused the supposed spread of these mutations.
Controversy
Although Chinese himself, Bruce Lahn's public announcements that some brain-genes are more advanced on some continents than on others were conscripted by websites promoting white "racialism". An American White supremacist magazine embraced the research as "the moment the antiracists and egalitarians have dreaded." John Derbyshire, writing in The National Review Online, wrote that as a result of the findings, "our cherished national dream of a well-mixed and harmonious meritocracy may be unattainable."
Lahn's study began to attract considerable controversy in the science world. Richard Lewontin considers the two published papers as "egregious examples of going well beyond the data to try to make a splash." Lahn maintains that the science of his studies are sound, and freely admits that a direct link between these particular genes and either cognition or intelligence has not yet been conclusively established. Bruce Lahn is now engaging himself with other areas of study.
Later genetic association studies by Mekel-Bobrov et al and Evans et al reported that the genotype for MCPH1 was under positive selection. Contrary to Lahn's speculation however they found no meaningful association with brain size and various cognitive measures, concluding that MCPH1 was not been selected for brain-related effects.
Other names
The microcephaly-related loci MCPH 3, 5 and 6 are usually classified by their alternate names CDK5RAP2, ASPM and CENPJ respectively, according to their other roles. (More information can be found from the articles dedicated to them and links in the information boxes.)
See also
References
- ^
Jackson, A.P.; et al. (2002). "Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain". Am. J. Hum. Genet. 71 (1): 136–142. doi:10.1086/341283. PMC 419993. PMID 12046007.
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Lin, S.Y. & Elledge, S.J. (2003). "Multiple tumor suppressor pathways negatively regulate telomerase". Cell. 113 (7): 881–889. doi:10.1016/S0092-8674(03)00430-6. PMID 12837246.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) -
Jackson, A.P.; et al. (1998). "Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter" (). Am. J. Hum. Genet. 63 (2): 541–546. doi:10.1086/301966. PMC 1377307. PMID 9683597.
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(help) - Wang, Y.Q. & B. Su (2004). "Molecular evolution of microcephalin, a gene determining human brain size". Hum. Mol. Genet. 13 (11): 1131–1137. doi:10.1093/hmg/ddh127. PMID 15056608.
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Evans, P.D.; et al. (2004). "Reconstructing the evolutionary history of microcephalin, a gene controlling human brain size". Hum. Mol. Genet. 13 (11): 1139–1145. doi:10.1093/hmg/ddh126. PMID 15056607.
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(help) - R.P. Woods; et al. (2006). "Normal variants of Microcephalin and ASPM do not account for brain size variability". Hum. Mol. Genet. 15 (12): 2025–2029. doi:10.1093/hmg/ddl126. PMID 16687438.
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(help) - J.P. Rushton, P.A. Vernon & T.A. Bons (2007). "No evidence that polymorphisms of brain regulator genes Microcephalin and ASPM are associated with general mental ability, head circumference or altruism". Biol. Lett. 3 (2): 157–160. doi:10.1098/rsbl.2006.0586. PMC 2104484. PMID 17251122.
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Evans, P.D.; et al. (2005). "Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans". Science. 309 (5741): 1717–20. doi:10.1126/science.1113722. PMID 16151009.
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ignored (help) - Ambrose, S.H. (1998). "Chronology of the Later Stone Age and food production in East Africa". J. Archaeol. Sci. 25 (4): 377–392. doi:10.1006/jasc.1997.0277.
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ignored (help) - Dediu, D. & D.R. Ladd (2007). "Linguistic tone is related to the population frequency of the adaptive haplogroups of two brain size genes, ASPM and Microcephalin". Proc. Nat. Acad. Sci. 104 (26): 10944. doi:10.1073/pnas.0610848104. PMC 1904158. PMID 17537923.
- PNAS article Evidence that the adaptive allele of the brain size gene microcephalin introgressed into Homo sapiens from an archaic Homo lineage Published online before print November 7, 2006 by Proceedings of the National Academy of Sciences of the USA
- Elizabeth Pennisi (2009). "NEANDERTAL GENOMICS: Tales of a Prehistoric Human Genome". Science. 323 (5916): 866–871. doi:10.1126/science.323.5916.866. PMID 19213888.
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ignored (help) - Richard E. Green; et al. (2010). "A Draft Sequence of the Neandertal Genome". Science. 328 (5979): 710–722. doi:10.1126/science.1188021. PMID 20448178.
{{cite journal}}
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(help) - Shimada MK, Panchapakesan K, Tishkoff SA, Nato AQ, Hey J (2007). "Divergent haplotypes and human history as revealed in a worldwide survey of X-linked DNA sequence variation". Mol. Biol. Evol. 24 (3): 687–98. doi:10.1093/molbev/msl196. PMID 17175528.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - Mekel-Bobrov, N.; et al. (2007). "The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence". Hum. Mol. Genet. 16 (6): adv. access. doi:10.1093/hmg/ddl487. PMID 17220170.
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(help) - Chris Brand (2005). "Race realism takes a step forward". American Renaissance. Retrieved 2008-09-21.
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ignored (help) - John Derbyshire (2005). "The specter of difference". National Review. Retrieved 2008-09-21.
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ignored (help) - scientists study of brain gene sparks a backlash
- Balter, M. (2006). "Bruce Lahn profile: Brain man makes waves with claims of recent human evolution". Science. 314 (5807): 1871–1873. doi:10.1126/science.314.5807.1871. PMID 17185582.
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ignored (help) - Timpson, N.; et al. (2007). "Comment on Papers by Evans et al. and Mekel-Bobrov et al. on Evidence for Positive Selection of MCPH1 and ASPM". Science. 317 (5841): 1036. doi:10.1126/science.1141705. PMID 17185582.
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External links
- Neanderthal Brains - a lecture by Bruce Lahn - from the NYAS podcasts.
- GeneReviews/NCBI/NIH/UW entry on Primary Autosomal Recessive Microcephaly
- Medterms
- JBC
- OUP Journals
- EMBL
- Bates, T; Luciano, M; Lind, P; Wright, M; Montgomery, G; Martin, N (2008). "Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language". Intelligence. 36: 689. doi:10.1016/j.intell.2008.04.001.