Cenedese Valentina, Mezzavilla Massimo, Morgan Anna, Marino Renato, Ettorre Cosimo Pietro, Margaglione Maurizio, Gasparini Paolo, Menini Anna
Neurobiology Group, SISSA, International School for Advanced Studies, Trieste, Italy.
Institute for Maternal and Child Health, Istituto Di Ricovero e Cura a Carattere Scientifico "Burlo Garofolo" and Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
PLoS One. 2015 Jan 30;10(1):e0116483. doi: 10.1371/journal.pone.0116483. eCollection 2015.
Type 3 Von Willebrand disease is an autosomal recessive disease caused by the virtual absence of the von Willebrand factor (VWF). A rare 253 kb gene deletion on chromosome 12, identified only in Italian and German families, involves both the VWF gene and the N-terminus of the neighbouring TMEM16B/ANO2 gene, a member of the family named transmembrane 16 (TMEM16) or anoctamin (ANO). TMEM16B is a calcium-activated chloride channel expressed in the olfactory epithelium. As a patient homozygous for the 253 kb deletion has been reported to have an olfactory impairment possibly related to the partial deletion of TMEM16B, we assessed the olfactory function in other patients using the University of Pennsylvania Smell Identification Test (UPSIT). The average UPSIT score of 4 homozygous patients was significantly lower than that of 5 healthy subjects with similar sex, age and education. However, 4 other members of the same family, 3 heterozygous for the deletion and 1 wild type, had a slightly reduced olfactory function indicating that socio-cultural or other factors were likely to be responsible for the observed difference. These results show that the ability to identify odorants of the homozygous patients for the deletion was not significantly different from that of the other members of the family, showing that the 253 kb deletion does not affect the olfactory performance. As other genes may compensate for the lack of TMEM16B, we identified some predicted functional partners from in silico studies of the protein-protein network of TMEM16B. Calculation of diversity for the corresponding genes for individuals of the 1000 Genomes Project showed that TMEM16B has the highest level of diversity among all genes of the network, indicating that TMEM16B may not be under purifying selection and suggesting that other genes in the network could compensate for its function for olfactory ability.
3型血管性血友病是一种常染色体隐性疾病,由血管性血友病因子(VWF)几乎完全缺失引起。仅在意大利和德国家庭中发现的12号染色体上一个罕见的253 kb基因缺失,涉及VWF基因和相邻的跨膜16B/anoctamin 2(TMEM16B/ANO2)基因的N端,TMEM16B/ANO2是跨膜16(TMEM16)或anoctamin(ANO)家族的成员。TMEM16B是一种在嗅觉上皮中表达的钙激活氯离子通道。由于据报道一名253 kb缺失的纯合患者存在可能与TMEM16B部分缺失相关的嗅觉障碍,我们使用宾夕法尼亚大学嗅觉识别测试(UPSIT)评估了其他患者的嗅觉功能。4名纯合患者的平均UPSIT得分显著低于5名性别、年龄和教育程度相似的健康受试者。然而,同一家族的其他4名成员,3名缺失杂合子和1名野生型,嗅觉功能略有下降,表明社会文化或其他因素可能是观察到的差异的原因。这些结果表明,缺失纯合患者识别气味的能力与家族其他成员没有显著差异,表明253 kb缺失不影响嗅觉表现。由于其他基因可能补偿TMEM16B的缺失,我们通过对TMEM16B蛋白质-蛋白质网络的计算机模拟研究确定了一些预测的功能伙伴。对千人基因组计划个体的相应基因多样性计算表明,TMEM16B在网络所有基因中具有最高水平的多样性,表明TMEM16B可能未受到纯化选择,并暗示网络中的其他基因可以补偿其嗅觉能力的功能。