Tanaka Akemi J, Cho Megan T, Millan Francisca, Juusola Jane, Retterer Kyle, Joshi Charuta, Niyazov Dmitriy, Garnica Adolfo, Gratz Edward, Deardorff Matthew, Wilkins Alisha, Ortiz-Gonzalez Xilma, Mathews Katherine, Panzer Karin, Brilstra Eva, van Gassen Koen L I, Volker-Touw Catharina M L, van Binsbergen Ellen, Sobreira Nara, Hamosh Ada, McKnight Dianalee, Monaghan Kristin G, Chung Wendy K
Department of Pediatrics, Columbia University Medical Center, New York, NY 10032, USA.
GeneDx, Gaithersburg, MD 20877, USA.
Am J Hum Genet. 2015 Sep 3;97(3):457-64. doi: 10.1016/j.ajhg.2015.07.014. Epub 2015 Aug 20.
Using whole-exome sequencing, we have identified in ten families 14 individuals with microcephaly, developmental delay, intellectual disability, hypotonia, spasticity, seizures, sensorineural hearing loss, cortical visual impairment, and rare autosomal-recessive predicted pathogenic variants in spermatogenesis-associated protein 5 (SPATA5). SPATA5 encodes a ubiquitously expressed member of the ATPase associated with diverse activities (AAA) protein family and is involved in mitochondrial morphogenesis during early spermatogenesis. It might also play a role in post-translational modification during cell differentiation in neuronal development. Mutations in SPATA5 might affect brain development and function, resulting in microcephaly, developmental delay, and intellectual disability.
通过全外显子组测序,我们在10个家族中鉴定出14名患有小头畸形、发育迟缓、智力障碍、肌张力减退、痉挛、癫痫、感音神经性听力损失、皮质视觉障碍的个体,以及精子发生相关蛋白5(SPATA5)中罕见的常染色体隐性预测致病变异。SPATA5编码一种与多种活动相关的ATP酶(AAA)蛋白家族中普遍表达的成员,并且在精子发生早期参与线粒体形态发生。它可能还在神经元发育过程中细胞分化的翻译后修饰中发挥作用。SPATA5中的突变可能影响大脑发育和功能,导致小头畸形、发育迟缓和智力障碍。