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遗传性脱发性毛囊角化病是由 MBTPS2 基因突变引起的。

Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2.

机构信息

Center of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Nederlands.

出版信息

Hum Mutat. 2010 Oct;31(10):1125-33. doi: 10.1002/humu.21335.

Abstract

Keratosis Follicularis Spinulosa Decalvans (KFSD) is a rare genetic disorder characterized by development of hyperkeratotic follicular papules on the scalp followed by progressive alopecia of the scalp, eyelashes, and eyebrows. Associated eye findings include photophobia in childhood and corneal dystrophy. Due to the genetic and clinical heterogeneity of similar disorders, a definitive diagnosis of KFSD is often challenging. Toward identification of the causative gene we reanalyzed a large Dutch KFSD family. SNP arrays (1 M) redefined the locus to a 2.9-Mb region at Xp22.12-Xp22.11. Screening of all 14 genes in the candidate region identified MBTPS2 as the candidate gene carrying a c.1523A>G (p.Asn508Ser) missense mutation. The variant was also identified in two unrelated X-linked KFSD families and cosegregated with KFSD in all families. In symptomatic female carriers, skewed X-inactivation of the normal allele matched with increased severity of symptoms. MBTPS2 is required for cleavage of sterol regulatory element-binding proteins (SREBPs). In vitro functional expression studies of the c.1523A>G mutation showed that sterol responsiveness was reduced by half. Other missense mutations in MBTPS2 have recently been identified in patients with IFAP syndrome. We postulate that both phenotypes are in the spectrum of one genetic disorder with a partially overlapping phenotype.

摘要

遗传性脱发性多发性外生性角化不良(KFSD)是一种罕见的遗传疾病,其特征是头皮出现角化过度的滤泡性丘疹,随后头皮、睫毛和眉毛逐渐脱发。相关的眼部表现包括儿童时期畏光和角膜营养不良。由于类似疾病具有遗传和临床异质性,因此通常难以明确诊断 KFSD。为了确定致病基因,我们重新分析了一个大型荷兰 KFSD 家族。SNP 芯片(1M)将该基因座重新定义为 Xp22.12-Xp22.11 上的 2.9Mb 区域。对候选区域中的所有 14 个基因进行筛选,发现 MBTPS2 是携带 c.1523A>G(p.Asn508Ser)错义突变的候选基因。该变体还在两个不相关的 X 连锁 KFSD 家族中被发现,并与所有家族中的 KFSD 共分离。在有症状的女性携带者中,正常等位基因的偏性 X 失活与症状的严重程度相匹配。MBTPS2 对于固醇调节元件结合蛋白(SREBPs)的切割是必需的。体外功能表达研究显示,c.1523A>G 突变使固醇反应性降低了一半。最近在 IFAP 综合征患者中也发现了 MBTPS2 的其他错义突变。我们推测这两种表型都属于一种遗传疾病的范畴,具有部分重叠的表型。

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