MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh EH4 2XU, UK.
BMC Genet. 2009 Dec 30;10:88. doi: 10.1186/1471-2156-10-88.
Eye and hair colour is highly variable in the European population, and is largely genetically determined. Both linkage and association studies have previously been used to identify candidate genes underlying this variation. Many of the genes found were previously known as underlying mutant mouse phenotypes or human genetic disease, but others, previously unsuspected as pigmentation genes, have also been discovered.
We assayed the hair of a population of individuals of Scottish origin using tristimulus colorimetry, in order to produce a quantitative measure of hair colour. Cluster analysis of this data defined two groups, with overlapping borders, which corresponded to visually assessed dark versus red/light hair colour. The Danish population was assigned into categorical hair colour groups. Both cohorts were also assessed for eye colour. DNA from the Scottish group was genotyped at SNPs in 33 candidate genes, using 384 SNPs identified by HapMap as representatives of each gene. Associations found between SNPs and colorimetric hair data and eye colour categories were replicated in a cohort of the Danish population. The Danish population was also genotyped with SNPs in 4 previously described pigmentation genes. We found replicable associations of hair colour with the KITLG and OCA2 genes. MC1R variation correlated, as expected, with the red dimension of colorimetric hair colour in Scots. The Danish analysis excluded those with red hair, and no associations were found with MC1R in this group, emphasising that MC1R regulates the colour rather than the intensity of pigmentation. A previously unreported association with the HPS3 gene was seen in the Scottish population. However, although this replicated in the smaller cohort of the Danish population, no association was seen when the whole study population was analysed.
We have found novel associations with SNPs in known pigmentation genes and colorimetrically assessed hair colour in a Scottish and a Danish population.
欧洲人群的眼睛和头发颜色高度多变,主要由遗传决定。先前已经使用连锁和关联研究来鉴定导致这种变化的候选基因。许多发现的基因以前是作为导致突变鼠表型或人类遗传疾病的基因,但也发现了其他以前不被认为是色素基因的基因。
我们使用三刺激比色法对一群具有苏格兰血统的个体的头发进行了检测,以产生头发颜色的定量测量值。对这些数据进行聚类分析定义了两个群体,边界重叠,对应于视觉评估的深色与红色/浅色头发颜色。丹麦人群被分配到分类头发颜色组中。两个队列也都评估了眼睛颜色。使用 HapMap 鉴定的代表每个基因的 384 个 SNP,对苏格兰组的 DNA 进行了 33 个候选基因的 SNP 基因分型。在丹麦人群的一个队列中复制了 SNP 与比色头发数据和眼睛颜色分类之间的关联。丹麦人群还使用 4 个先前描述的色素基因的 SNP 进行了基因分型。我们发现头发颜色与 KITLG 和 OCA2 基因之间存在可复制的关联。正如预期的那样,MC1R 变异与苏格兰人比色头发颜色的红色维度相关。丹麦分析排除了红发者,并且在该组中没有发现与 MC1R 的关联,这强调了 MC1R 调节颜色而不是色素沉着的强度。在苏格兰人群中观察到与 HPS3 基因的先前未报道的关联。然而,尽管在丹麦人群的较小队列中复制了该关联,但当分析整个研究人群时,没有发现关联。
我们在苏格兰和丹麦人群中发现了与已知色素基因和比色评估的头发颜色的 SNP 的新关联。