Shylo Natalia A, Christopher Kasey J, Iglesias Alejandro, Daluiski Aaron, Weatherbee Scott D
Department of Genetics, Yale University, School of Medicine, P.O. Box 208005, SHM I-142D, 333 Cedar Street, New Haven, CT, 06520.
Division of Clinical Genetics, Department of Pediatrics, Columbia University Medical Center, New York, New York.
Hum Mutat. 2016 Feb;37(2):155-9. doi: 10.1002/humu.22925. Epub 2015 Nov 23.
The proximate causes of multiple human genetic syndromes (ciliopathies) are disruptions in the formation or function of the cilium, an organelle required for a multitude of developmental processes. We previously identified Tmem107 as a critical regulator of cilia formation and embryonic organ development in the mouse. Here, we describe a patient with a mutation in TMEM107 that developed atypical Orofaciodigital syndrome (OFD), and show that the OFD patient shares several morphological features with the Tmem107 mutant mouse including polydactyly and reduced numbers of ciliated cells. We show that TMEM107 appears to function within cilia to regulate protein content, as key ciliary proteins do not localize normally in cilia derived from the Tmem107 mouse mutant and the human patient. These data indicate that TMEM107 plays a key, conserved role in regulating ciliary protein composition, and is a novel candidate for ciliopathies of unknown etiology.
多种人类遗传综合征(纤毛病)的直接病因是纤毛(一种众多发育过程所必需的细胞器)形成或功能的破坏。我们之前鉴定出Tmem107是小鼠纤毛形成和胚胎器官发育的关键调节因子。在此,我们描述了一名患有TMEM107突变的患者,该患者患有一种非典型口面指综合征(OFD),并表明该OFD患者与Tmem107突变小鼠具有若干形态学特征,包括多指畸形和纤毛细胞数量减少。我们表明,TMEM107似乎在纤毛内发挥作用以调节蛋白质含量,因为关键的纤毛蛋白在源自Tmem107小鼠突变体和人类患者的纤毛中不能正常定位。这些数据表明,TMEM107在调节纤毛蛋白组成方面发挥关键的保守作用,并且是病因不明的纤毛病的一个新候选因素。