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节俭基因型假说及其对人类复杂遗传疾病研究的启示。

The thrifty-genotype hypothesis and its implications for the study of complex genetic disorders in man.

作者信息

Sharma A M

机构信息

Medizinische Klinik IV, Klinikum Benjamin Franklin, Freie Universität Berlin, Germany.

出版信息

J Mol Med (Berl). 1998 Jul;76(8):568-71. doi: 10.1007/s001090050251.

Abstract

According to the "thrifty-genotype" hypothesis proposed by Neel, diseases of civilization such as non-insulin-dependent diabetes mellitus and hypertension result from a discordance between certain features of our present-day environment and our genetic make-up which evolved to fit the life of Paleolithic humans. This concept implies that while "affected" individuals harbor the "original" ancestral version of the relevant genes, healthy or "unaffected" individuals have picked up recent mutations leading to a "loss of thriftiness" of these genes. Support for this concept now comes from recent studies of the angiotensinogen gene, where an ancestral variant of the gene (AGT 235T), also present in primates, has now been associated with hypertension whereas a neomorphic variant (AGT 235M) apparently reduces the risk of high blood pressure. The implications of these findings for our understanding and approach to the study of complex genetic diseases is discussed.

摘要

根据尼尔提出的“节俭基因型”假说,诸如非胰岛素依赖型糖尿病和高血压等文明病是由我们当今环境的某些特征与我们为适应旧石器时代人类生活而进化出的基因构成之间的不协调所导致的。这一概念意味着,虽然“患病”个体携带相关基因的“原始”祖先版本,但健康或“未患病”个体发生了近期突变,导致这些基因出现“节俭性丧失”。现在,对这一概念的支持来自对血管紧张素原基因的最新研究,该基因的一个祖先变体(AGT 235T)在灵长类动物中也存在,现在已与高血压相关联,而一个新形态变体(AGT 235M)显然降低了患高血压的风险。本文讨论了这些发现对我们理解和研究复杂遗传疾病方法的影响。

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