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丘疹性皮损型无毛症患者无毛基因遗传缺陷的鉴定:遗传性无毛症表型异质性的证据

Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias.

作者信息

Sprecher E, Bergman R, Szargel R, Friedman-Birnbaum R, Cohen N

机构信息

Department of Dermatology, Rambam Medical Center, Technion-Israel Institute of Technology, Haifa 31096, Israel.

出版信息

Am J Hum Genet. 1999 May;64(5):1323-9. doi: 10.1086/302368.

Abstract

Recently, we showed that atrichia with papular lesions (APL), a rare inherited form of alopecia, is transmitted as an autosomal recessive trait in a large inbred kindred of Israeli-Arab origin. Furthermore, we mapped the APL locus to a 5-cM region of chromosome 8p12 in this family. The human "hairless" gene is a candidate target gene for the disease mutation because it maps to the APL locus and because it was recently found to be mutated in a related but clinically distinct form of alopecia known as "alopecia universalis" or "congenital alopecia." In the present study, the coding sequence of the hairless gene was compared by reverse transcription-PCR in fibroblast cell lines derived from an affected patient and an unrelated individual. We identified a single-base deletion (3434delC) in the hairless gene that cosegregated with the disease phenotype in the family. This deletion is predicted to cause a frameshift mutation in the highly conserved C-terminal part of the hairless protein, a region putatively involved in the transcription factor activity of the hairless gene product. The present results are indicative of phenotypic heterogeneity in inherited atrichias caused by mutations in the hairless gene, suggesting different roles for the regions mutated in APL and in other forms of congenital atrichia during hair development.

摘要

最近,我们发现丘疹性秃发(APL),一种罕见的遗传性脱发形式,在一个源自以色列阿拉伯的大型近亲家族中作为常染色体隐性性状遗传。此外,我们将该家族中的APL基因座定位到8号染色体p12的一个5厘摩区域。人类“无毛”基因是该疾病突变的候选靶基因,因为它定位于APL基因座,且最近发现它在一种相关但临床特征不同的脱发形式中发生突变,这种脱发形式被称为“全秃”或“先天性秃发”。在本研究中,通过逆转录-聚合酶链反应比较了来自一名患病患者和成纤维细胞系的无关个体的无毛基因编码序列。我们在无毛基因中鉴定出一个单碱基缺失(3434delC),它与该家族中的疾病表型共分离。预计这种缺失会在无毛蛋白高度保守的C末端部分引起移码突变,该区域可能参与无毛基因产物的转录因子活性。目前的结果表明,由无毛基因突变引起的遗传性脱发存在表型异质性,这表明在APL和其他形式的先天性脱发中发生突变的区域在毛发发育过程中具有不同的作用。

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1
Atrichia with papular lesions.无毛发伴丘疹性损害。
Dermatologica. 1961 Feb;122:85-9. doi: 10.1159/000255187.

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