Suppr超能文献

在英国双胞胎队列中,利用双能X线吸收测定成像技术对5号染色体上骨长度的数量性状基因座进行研究。

Quantitative trait loci for bone lengths on chromosome 5 using dual energy X-Ray absorptiometry imaging in the Twins UK cohort.

作者信息

Chinappen-Horsley Usha, Blake Glen M, Fogelman Ignac, Kato Bernet, Ahmadi Kourosh R, Spector Tim D

机构信息

Twin Research and Genetic Epidemiology Unit, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom.

出版信息

PLoS One. 2008 Mar 12;3(3):e1752. doi: 10.1371/journal.pone.0001752.

Abstract

Human height is a highly heritable and complex trait but finding important genes has proven more difficult than expected. One reason might be the composite measure of height which may add heterogeneity and noise. The aim of this study was to conduct a genome-wide linkage scan to identify quantitative trait loci (QTL) for lengths of spine, femur, tibia, humerus and radius. These were investigated as alternative measures for height in a large, population-based twin sample with the potential to find genes underlying bone size and bone diseases. 3,782 normal Caucasian females, 18-80 years old, with whole body dual energy X-ray absorptiometry (DXA) images were used. A novel and reproducible method, linear pixel count (LPC) was used to measure skeletal sizes on DXA images. Intraclass correlations and heritability estimates were calculated for lengths of spine, femur, tibia, humerus and radius on monozygotic (MZ; n = 1,157) and dizygotic (DZ; n = 2,594) twins. A genome-wide linkage scan was performed on 2000 DZ twin subjects. All skeletal sites excluding spine were highly correlated. Intraclass correlations showed results for MZ twins to be significantly higher than DZ twins for all traits. Heritability results were as follows: spine, 66%; femur, 73%; tibia, 65%; humerus, 57%; radius, 68%. Results showed reliable evidence of highly suggestive linkage on chromosome 5 for spine (LOD score = 3.0) and suggestive linkage for femur (LOD score = 2.19) in the regions of 105cM and 155cM respectively. We have shown strong heritability of all skeletal sizes measured in this study and provide preliminary evidence that spine length is linked to the chromosomal region 5q15-5q23.1. Bone size phenotype appears to be more useful than traditional height measures to uncover novel genes. Replication and further fine mapping of this region is ongoing to determine potential genes influencing bone size and diseases affecting bone.

摘要

人类身高是一种高度可遗传的复杂性状,但发现重要基因比预期的更困难。一个原因可能是身高的综合测量,这可能会增加异质性和噪声。本研究的目的是进行全基因组连锁扫描,以确定脊柱、股骨、胫骨、肱骨和桡骨长度的数量性状位点(QTL)。在一个基于人群的大型双胞胎样本中,将这些作为身高的替代测量指标进行研究,有可能找到影响骨大小和骨疾病的潜在基因。研究使用了3782名18至80岁的正常白种女性,她们都有全身双能X线吸收测定(DXA)图像。一种新颖且可重复的方法,即线性像素计数(LPC),用于测量DXA图像上的骨骼大小。计算了单卵双胞胎(MZ;n = 1157)和双卵双胞胎(DZ;n = 2594)的脊柱、股骨、胫骨、肱骨和桡骨长度的组内相关性和遗传度估计值。对2000名DZ双胞胎受试者进行了全基因组连锁扫描。除脊柱外,所有骨骼部位都高度相关。组内相关性显示,所有性状的MZ双胞胎结果均显著高于DZ双胞胎。遗传度结果如下:脊柱66%;股骨73%;胫骨65%;肱骨57%;桡骨68%。结果显示,在5号染色体上,脊柱有高度提示性连锁的可靠证据(LOD得分 = 3.0),股骨在105cM和155cM区域有提示性连锁(LOD得分 = 2.19)。我们已经证明了本研究中测量的所有骨骼大小都具有很强的遗传性,并提供了初步证据表明脊柱长度与染色体区域5q15 - 5q23.1相关。骨大小表型似乎比传统身高测量更有助于发现新基因。正在对该区域进行重复研究和进一步精细定位,以确定影响骨大小的潜在基因以及影响骨骼的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c5a/2262137/363162568b96/pone.0001752.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验