Li Xin, Hu Jintian, Zhang Jiao, Jin Qian, Wang Duen-Mei, Yu Jun, Zhang Qingguo, Zhang Yong-Biao
Beijing Institute of Genomics, Chinese Academy of Sciences and Key Laboratory of Genome Science and Information, Chinese Academy of Sciences, Beijing, P. R. China; Department of Cardiology, Beijing Anzhen Hospital of the Capital University of Medical Sciences, Beijing, P. R. China.
Department of Ear Reconstruction, Plastic Surgery Hospital, Chinese Academy of Medical Sciences, Beijing, P.R. China.
PLoS One. 2014 Jul 1;9(7):e101152. doi: 10.1371/journal.pone.0101152. eCollection 2014.
Microtia is a congenital deformity where the external ear is underdeveloped. Genetic investigations have identified many susceptibility genes of microtia-related syndromes. However, no causal genes were reported for isolated microtia, the main form of microtia. We conducted a genome-wide linkage analysis on a 5-generation Chinese pedigree with isolated bilateral microtia. We identified a suggestive linkage locus on 4p15.32-4p16.2 with parametric LOD score of 2.70 and nonparametric linkage score (Zmean) of 12.28 (simulated occurrence per genome scan equal to 0.46 and 0.47, respectively). Haplotype reconstruction analysis of the 4p15.32-4p16.2 region further confined the linkage signal to a 10-Mb segment located between rs12505562 and rs12649803 (9.65-30.24 cM; 5.54-15.58 Mb). Various human organ developmental genes reside in this 10-Mb susceptibility region, such as EVC, EVC2, SLC2A9, NKX3-2, and HMX1. The coding regions of three genes, EVC known for cartilage development and NKX3-2, HMX1 involved in microtia, were selected for sequencing with 5 individuals from the pedigree. Of the 38 identified sequence variants, none segregates along with the disease phenotype. Other genes or DNA sequences of the 10-Mb region warrant for further investigation. In conclusion, we report a susceptibility locus of isolated microtia, and this finding will encourage future studies on the genetic basis of ear deformity.
小耳畸形是一种先天性畸形,其外耳发育不全。基因研究已经确定了许多与小耳畸形相关综合征的易感基因。然而,对于小耳畸形的主要形式——散发性小耳畸形,尚未有因果基因的报道。我们对一个患有双侧散发性小耳畸形的五代中国家系进行了全基因组连锁分析。我们在4p15.32 - 4p16.2区域鉴定出一个提示性连锁位点,参数化LOD得分为2.70,非参数连锁得分(Zmean)为12.28(每次基因组扫描的模拟发生率分别为0.46和0.47)。对4p15.32 - 4p16.2区域的单倍型重建分析进一步将连锁信号限定在位于rs12505562和rs12649803之间的10 Mb片段(9.65 - 30.24 cM;5.54 - 15.58 Mb)。多种人类器官发育基因存在于这个10 Mb的易感区域,如EVC、EVC2、SLC2A9、NKX3 - 2和HMX1。选择了三个基因的编码区进行测序,其中EVC以软骨发育闻名,NKX3 - 2和HMX1与小耳畸形有关,对家系中的5名个体进行了测序。在鉴定出的38个序列变异中,没有一个与疾病表型共分离。10 Mb区域的其他基因或DNA序列值得进一步研究。总之,我们报告了散发性小耳畸形的一个易感位点,这一发现将促进未来对耳部畸形遗传基础的研究。