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一种导致多种剪接重排的新型转谷氨酰胺酶1(TGM1)突变与常染色体隐性先天性鱼鳞病相关。

A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis.

作者信息

Ortega-Recalde O, Moreno M B, Vergara J I, Fonseca D J, Rojas R F, Mosquera H, Medina C L, Restrepo C M, Laissue P

机构信息

Genetics Unit, GENIUROS Group, Escuela de Medicina y Ciencias de la Salud, Universidad del Rosario, Bogotá, Colombia.

Department of Dermatology, Universidad Autónoma de Bucaramanga, Bucaramanga, Colombia.

出版信息

Clin Exp Dermatol. 2015 Oct;40(7):757-60. doi: 10.1111/ced.12627. Epub 2015 Mar 9.

Abstract

Autosomal recessive congenital ichthyosis (ARCI) is a group of rare, clinically heterogeneous skin disorders that affect cornification. ARCI includes lamellar ichthyosis, congenital ichthyosiform erythroderma and harlequin ichthyosis. TGM1 mutations cause > 50% of ARCI cases in the USA. We report two siblings with ARCI. They were found to carry a novel aetiological TGM1 mutation, which leads to the synthesis of multiple abnormal transcripts. These molecules resulted from three independent mechanisms: intron retention, exon skipping and activation of expand cryptic splice sites. Taken together, our findings expand the known TGM1 mutation repertoire, and provide an insight into the molecular mechanisms leading to ARCI phenotypes. These results could be useful for genetic counselling and future potential genotype-phenotype correlations.

摘要

常染色体隐性先天性鱼鳞病(ARCI)是一组影响角质化的罕见的、临床异质性皮肤疾病。ARCI包括板层状鱼鳞病、先天性鱼鳞病样红皮病和丑角鱼鳞病。在美国,超过50%的ARCI病例由转谷氨酰胺酶1(TGM1)突变引起。我们报告了两名患有ARCI的兄弟姐妹。他们被发现携带一种新的致病TGM1突变,该突变导致多种异常转录本的合成。这些分子由三种独立机制产生:内含子保留、外显子跳跃和隐匿性剪接位点的激活。综合来看,我们的研究结果扩展了已知的TGM1突变库,并深入了解了导致ARCI表型的分子机制。这些结果可能有助于遗传咨询和未来潜在的基因型-表型相关性研究。

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