AI Article Synopsis

  • The study sequenced 114 genes related to key biological processes in a diverse human population and found a notable increase in functional genetic variations at a minor allele frequency around 6%.
  • The researchers measured functionality by comparing nonsynonymous SNPs (which change protein sequences) to synonymous or intron SNPs, noting a stable trend at low frequencies that sharply declines after reaching 6%.
  • Four potential explanations for this threshold effect were proposed: the presence of harmful variants, balancing selection favoring heterozygotes, population-specific genetic variations, and the accumulation of adaptive variants due to significant environmental changes over the past 7,000 to 17,000 years.

Article Abstract

We sequenced 114 genes (for DNA repair, cell cycle arrest, apoptosis, and detoxification)in a mixed human population and observed a sudden increase in the number of functional polymorphisms below a minor allele frequency of approximately 6%. Functionality is assessed by considering the ratio in the number of nonsynonymous single nucletide polymorphisms (SNPs)to the number of synonymous or intron SNPs. This ratio is steady from below 1% in frequency-that regime traditionally associated with rare Mendelian diseases-all the way up to about 6% in frequency, after which it falls precipitously. We consider possible explanations for this threshold effect. There are four candidates as follows: (1). deleterious variants that have yet to be purified from the population, (2). balancing selection, in which a selective advantage accrues to the heterozygotes, (3). population-specific functional polymorphisms, and (4). adaptive variants that are accumulating in the population as a response to the dramatic environmental changes of the last 7000 approximately 17000 years.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC403778PMC
http://dx.doi.org/10.1101/gr.1324303DOI Listing

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