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印度同族通婚人群(吠陀族)人体测量不对称性的遗传学研究

Genetics of anthropometric asymmetry in an Indian endogamous population-Vaidyas.

作者信息

Sengupta Mahua, Karmakar Bibha

机构信息

Biological Anthropology Unit, Indian Statistical Institute, Kolkata 700 108, India.

出版信息

Am J Hum Biol. 2007 May-Jun;19(3):399-408. doi: 10.1002/ajhb.20601.

Abstract

To understand the genetics of Fluctuating Asymmetry (FA) and Directional Asymmetry (DA), the present study comprised 14 bilateral morphometric traits from 200 Vaidya families including 824 individuals (of two generations) from North 24 Parganas, West Bengal. The statistical analysis included: Regression analysis to remove the age effect, Familial correlation, Heritability estimation, Principal Component Analysis and Segregation Analysis (SA) using genetic model test. The obtained results revealed little effect of genetic factor and considerable amount of environmental influence on anthropometric asymmetry. The results support the idea postulated by several previous authors that FA provides a measure of developmental instability in man. The contribution of heredity on these asymmetric variables is not unimportant but that of the common environment is very substantial. The magnitude of heritability of DA traits is slightly higher than that of FA traits. Five principal factors were detected from these asymmetric traits (three factors are on asymmetry on length, head, and breadth; while last two factors represent the asymmetry of diameters). SA did not suggest any evidence of major gene contribution. But the involvement of minor genes or polygenes could not be discarded. As the study on SA of asymmetry in man is limited, similar other studies are needed to confirm the result of the present study.

摘要

为了解波动不对称性(FA)和定向不对称性(DA)的遗传学,本研究纳入了来自北24区帕加纳斯、西孟加拉邦的200个吠陀家庭的14项双侧形态测量特征,包括824名(两代人)个体。统计分析包括:用于消除年龄效应的回归分析、家族相关性分析、遗传力估计、主成分分析以及使用遗传模型检验的分离分析(SA)。所得结果显示,遗传因素对人体测量不对称性影响较小,而环境影响相当大。这些结果支持了几位先前作者提出的观点,即FA为衡量人类发育不稳定性提供了一种方法。遗传因素对这些不对称变量的贡献并非不重要,但共同环境的贡献非常显著。DA特征的遗传力大小略高于FA特征。从这些不对称特征中检测到五个主要因素(三个因素涉及长度、头部和宽度的不对称性;而最后两个因素代表直径的不对称性)。SA未表明有任何主基因贡献的证据。但不能排除微基因或多基因的参与。由于对人类不对称性的SA研究有限,需要开展类似的其他研究来证实本研究结果。

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