Suppr超能文献

X连锁肾上腺脑白质营养不良患者的异常信使核糖核酸表达及错义突变。

Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy.

作者信息

Cartier N, Sarde C O, Douar A M, Mosser J, Mandel J L, Aubourg P

机构信息

INSERM U342, Hôpital Saint Vincent de Paul, Paris, France.

出版信息

Hum Mol Genet. 1993 Nov;2(11):1949-51. doi: 10.1093/hmg/2.11.1949.

Abstract

A candidate gene for X-linked adrenoleukodystrophy (ALD) has been identified via positional cloning strategies. We now report messenger RNA expression in fibroblasts from 6 unrelated ALD patients. Four patients lacked the normal 4.2 kb transcript, three of them having deletions of the ALD gene. A fifth patient with a deletion of 1.6 kb had a smaller 4.0 kb transcript. The last patient had a normal sized transcript and a missense mutation at base 1258 leading to Glu-291-Lys substitution in a region of the candidate gene protein which is conserved in the 70 kD peroxisomal membrane protein. These results provide further evidence that this candidate gene is indeed the ALD gene.

摘要

通过定位克隆策略已鉴定出一个与X连锁肾上腺脑白质营养不良(ALD)相关的候选基因。我们现在报告6名无亲缘关系的ALD患者成纤维细胞中的信使核糖核酸表达情况。4名患者缺乏正常的4.2 kb转录本,其中3名患者存在ALD基因缺失。第五名患者有1.6 kb的缺失,其转录本为较小的4.0 kb。最后一名患者转录本大小正常,但在第1258位碱基处有一个错义突变,导致候选基因蛋白区域中的Glu-291-Lys替换,该区域在70 kD过氧化物酶体膜蛋白中保守。这些结果进一步证明该候选基因确实是ALD基因。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验