Centre National de la Recherche Scientifique, Institut de Génétique et Développement de Rennes, Rennes, France.
Nat Genet. 2012 Jan 15;44(2):140-7. doi: 10.1038/ng.1056.
Ichthyoses comprise a heterogeneous group of genodermatoses characterized by abnormal desquamation over the whole body, for which the genetic causes of several human forms remain unknown. We used a spontaneous dog model in the golden retriever breed, which is affected by a lamellar ichthyosis resembling human autosomal recessive congenital ichthyoses (ARCI), to carry out a genome-wide association study. We identified a homozygous insertion-deletion (indel) mutation in PNPLA1 that leads to a premature stop codon in all affected golden retriever dogs. We subsequently found one missense and one nonsense mutation in the catalytic domain of human PNPLA1 in six individuals with ARCI from two families. Further experiments highlighted the importance of PNPLA1 in the formation of the epidermal lipid barrier. This study identifies a new gene involved in human ichthyoses and provides insights into the localization and function of this yet uncharacterized member of the PNPLA protein family.
鱼鳞病是一组由基因引起的皮肤疾病,其特征为全身异常脱屑,几种人类形式的遗传原因仍不清楚。我们使用了一种自发性犬模型——金毛猎犬,其患有板层状鱼鳞病,类似于人类常染色体隐性先天性鱼鳞病(ARCI),进行了全基因组关联研究。我们在所有受影响的金毛猎犬中发现了 PNPLA1 基因的纯合插入缺失(indel)突变,导致所有受影响的金毛猎犬都出现了过早的终止密码子。随后,在来自两个家族的六名 ARCI 个体的人类 PNPLA1 的催化结构域中发现了一个错义突变和一个无义突变。进一步的实验强调了 PNPLA1 在表皮脂质屏障形成中的重要性。本研究确定了一个新的与人类鱼鳞病相关的基因,并为该尚未被描述的 PNPLA 蛋白家族成员的定位和功能提供了新的见解。