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首页> 外文期刊>Human Biology: Official Publication of the Human Biology Council >Extending Genome-wide Association Study Results to Test Classic Anthropological Hypotheses: Human Third Molar Agenesis and the 'Probable Mutation Effect'
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Extending Genome-wide Association Study Results to Test Classic Anthropological Hypotheses: Human Third Molar Agenesis and the 'Probable Mutation Effect'

机译:扩展基因组关联研究结果以测试经典人类学假设:人类第三摩尔刺激和“可能的突变效应”

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A genome-wide association study (GWAS) identifies regions of the genome that likely afffect the variable state of a phenotype of interest. These regions can then be studied with population genetic methods to make inferences about the evolutionary history of the trait. There are increasing opportunities to use GWAS results-even from clinically motivated studies-for tests of classic anthropological hypotheses. One such example, presented here as a case study for this approach, involves tooth development variation related to dental crowding. Specifically, more than 10% of humans fail to develop one or more permanent third molars (M3 agenesis). M3 presence/absence variation within human populations has a significant genetic component (heritability estimate h(2) = 0.47). The evolutionary significance of M3 agenesis has a long history of anthropological speculation. First, the modern frequency of M3 agenesis could reflect a relaxation of selection pressure to retain larger and more teeth following the origins of cooking and other food-softening behaviors (i.e., the genetic drift hypothesis or, classically, the "probable mutation efffect"). Alternatively, commensurate with increasing hominin brain size and facial shortening, M3 agenesis may have conferred an adaptive fitness advantage if it reduced the risk of M3 impaction and potential health complications (i.e., the positive selection hypothesis). A recent GWAS identified 70 genetic loci that may play a role in human M3 presence/absence variation. To begin evaluating the contrasting evolutionary scenarios for M3 agenesis, we used the integrated haplotype score (iHS) statistic to test whether those 70 genetic regions are enriched for genomic signatures of recent positive selection. None of our findings are inconsistent with the null hypothesis of genetic drift to explain the high prevalence of human M3 agenesis. This result might suggest that M3 impaction rates for modern humans do not accurately retrodict those of the preagricultural past. Alternatively, the absence of support for the positive selection hypothesis could reflect a lack of power; this analysis should be repeated following the completion of more comprehensive GWAS analyses for human M3 agenesis.
机译:一个基因组 - 范围的协会研究(GWAs)识别可能相应于感兴趣表型的可变状态的基因组的区域。然后可以用群体遗传方法研究这些区域,以便对特性的进化史进行推断。越来越多的机会使用GWAS结果 - 即使来自临床动机研究 - 用于经典人类学假设的测试。这里呈现的一个这样的例子作为这种方法的案例研究,涉及与牙科拥挤有关的牙齿开发变化。具体而言,超过10%的人类未能发展一种或多种永久性的第三磨牙(M3刺激)。人群中的M3存在/不存在变化具有显着的遗传组分(遗传性估计H(2)= 0.47)。 M3患者的进化意义具有悠久的人类猜测历史。首先,M3衰老的现代频率可以反映选择压力的放松,以便在烹饪和其他食物软化行为的起源之后保持较大,更牙齿(即遗传漂移假说或经典,“可能的突变efffect”) 。或者,随着MAININ脑大小和面部缩短的增加,M3衰退可能已经赋予了适应性的适应性优势,如果降低M3冒号和潜在的健康并发症(即阳性选择假说)。最近的Gwas确定了70个遗传基因座,其可能在人M3存在/缺失变化中发挥作用。为了开始评估M3患者的对比化进化场景,我们使用集成的单倍型评分(IHS)统计学来测试这些70个遗传区域是否富集近期阳性选择的基因组特征。我们的发现都不是与遗传漂移的零假设不一致,以解释人体M3的高患病率。这一结果可能表明现代人类的M3拨款率不准确地撤销血统过去的那些。或者,没有对阳性选择假设的支持可能会反映缺乏力量;在完成更全面的GWAS分析后,应重复该分析,用于人体M3刺激。

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