PloS Genetics:用五个基因勾勒出你的面容
导读 | 华人科学家Liu等人研究指出只需要五个基因便能够勾勒出一个人的面容,这一则消息应该会让警察很开心,以后要抓犯罪嫌疑人,通过DNA技术便能预先知道他的容貌,这让警察可以省很多力气。同样,对于想知道未出生的胎儿模样的准父母来说,也是件有趣的事情。
<a href="http://img.360zhyx.com/uploads/2012/09/journal.pgen_.10029... |
华人科学家Liu等人研究指出只需要五个基因便能够勾勒出一个人的面容,这一则消息应该会让警察很开心,以后要抓犯罪嫌疑人,通过DNA技术便能预先知道他的容貌,这让警察可以省很多力气。同样,对于想知道未出生的胎儿模样的准父母来说,也是件有趣的事情。
<a href="http://img.360zhyx.com/uploads/2012/09/journal.pgen_.1002932.g005.png"><img class="aligncenter size-full wp-image-4050" title="journal.pgen.1002932.g005" src="http://img.360zhyx.com/uploads/2012/09/journal.pgen_.1002932.g005.png" alt="" width="320" height="636" /><!--more--></a>
参考文献:
A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans
Inter-individual variation in facial shape is one of the most noticeable phenotypes in humans, and it is clearly under genetic regulation; however, almost nothing is known about the genetic basis of normal human facial morphology. We therefore conducted a genome-wide association study for facial shape phenotypes in multiple discovery and replication cohorts, considering almost ten thousand individuals of European descent from several countries. Phenotyping of facial shape features was based on landmark data obtained from three-dimensional head magnetic resonance images (MRIs) and two-dimensional portrait images. We identified five independent genetic loci associated with different facial phenotypes, suggesting the involvement of five candidate genes—PRDM16, PAX3, TP63, C5orf50, and COL17A1—in the determination of the human face. Three of them have been implicated previously in vertebrate craniofacial development and disease, and the remaining two genes potentially represent novel players in the molecular networks governing facial development. Our finding at PAX3 influencing the position of the nasion replicates a recent GWAS of facial features. In addition to the reported GWA findings, we established links between common DNA variants previously associated with NSCL/P at 2p21, 8q24, 13q31, and 17q22 and normal facial-shape variations based on a candidate gene approach. Overall our study implies that DNA variants in genes essential for craniofacial development contribute with relatively small effect size to the spectrum of normal variation in human facial morphology. This observation has important consequences for future studies aiming to identify more genes involved in the human facial morphology, as well as for potential applications of DNA prediction of facial shape such as in future forensic applications.
文献链接:<a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002932">http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002932</a>
<br/>来源:全球分子诊断网
<a href="http://img.360zhyx.com/uploads/2012/09/journal.pgen_.1002932.g005.png"><img class="aligncenter size-full wp-image-4050" title="journal.pgen.1002932.g005" src="http://img.360zhyx.com/uploads/2012/09/journal.pgen_.1002932.g005.png" alt="" width="320" height="636" /><!--more--></a>
参考文献:
A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans
Inter-individual variation in facial shape is one of the most noticeable phenotypes in humans, and it is clearly under genetic regulation; however, almost nothing is known about the genetic basis of normal human facial morphology. We therefore conducted a genome-wide association study for facial shape phenotypes in multiple discovery and replication cohorts, considering almost ten thousand individuals of European descent from several countries. Phenotyping of facial shape features was based on landmark data obtained from three-dimensional head magnetic resonance images (MRIs) and two-dimensional portrait images. We identified five independent genetic loci associated with different facial phenotypes, suggesting the involvement of five candidate genes—PRDM16, PAX3, TP63, C5orf50, and COL17A1—in the determination of the human face. Three of them have been implicated previously in vertebrate craniofacial development and disease, and the remaining two genes potentially represent novel players in the molecular networks governing facial development. Our finding at PAX3 influencing the position of the nasion replicates a recent GWAS of facial features. In addition to the reported GWA findings, we established links between common DNA variants previously associated with NSCL/P at 2p21, 8q24, 13q31, and 17q22 and normal facial-shape variations based on a candidate gene approach. Overall our study implies that DNA variants in genes essential for craniofacial development contribute with relatively small effect size to the spectrum of normal variation in human facial morphology. This observation has important consequences for future studies aiming to identify more genes involved in the human facial morphology, as well as for potential applications of DNA prediction of facial shape such as in future forensic applications.
文献链接:<a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002932">http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1002932</a>
<br/>来源:全球分子诊断网
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