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基因型与表型:人类色素沉着

Genotype versus phenotype: human pigmentation.

作者信息

Tully Gillian

机构信息

The Forensic Science Service Ltd., Trident Court, Solihull Parkway, Birmingham B37 7YN, United Kingdom.

出版信息

Forensic Sci Int Genet. 2007 Jun;1(2):105-10. doi: 10.1016/j.fsigen.2007.01.005. Epub 2007 Mar 1.

Abstract

The natural range of hair and skin colour is a continuous spectrum, controlled by multiple genes in a complex fashion. Many of these genes are as yet unknown, but several key pigmentation genes have been characterised, in particular the melanocortin 1 receptor gene (MC1R). Here, the function and known mutations of MC1R and other human pigmentation genes including ASIP, MATP, SLC24A5, TYR, TYRP1 and OCA2 are outlined, and a forensic test based on MC1R SNPs presented. The forensic utility of this and potential future genetic tests for phenotypic traits are discussed, in the light of the extensive debate on the ethics of predicting phenotypic traits from crime scene samples.

摘要

头发和肤色的自然范围是一个连续的光谱,由多个基因以复杂的方式控制。其中许多基因尚不清楚,但已经鉴定出几个关键的色素沉着基因,特别是黑皮质素1受体基因(MC1R)。本文概述了MC1R以及其他人类色素沉着基因(包括ASIP、MATP、SLC24A5、TYR、TYRP1和OCA2)的功能和已知突变,并介绍了一种基于MC1R单核苷酸多态性的法医检测方法。鉴于从犯罪现场样本预测表型特征的伦理问题存在广泛争议,本文讨论了该检测方法以及未来潜在的表型特征基因检测方法在法医领域的实用性。

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