Suppr超能文献

对色素失禁症杂合子女性中致死等位基因的选择。

Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

作者信息

Migeon B R, Axelman J, Jan de Beur S, Valle D, Mitchell G A, Rosenbaum K N

机构信息

Department of Pediatrics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Am J Hum Genet. 1989 Jan;44(1):100-6.

Abstract

Studies of five heterozygous females from three kindreds segregating incontinentia pigmenti indicate that cells expressing the mutation have been eliminated from skin fibroblast cultures and in varying degrees from hematopoietic tissues. Clonal analysis was carried out using G6PD variants and methylation patterns at the HPRT locus. Our results confirm X linkage in these families and suggest that selection against cells expressing mutations that are lethal to males in utero may help ameliorate the deleterious phenotype in carrier females.

摘要

对来自三个分离色素失禁症的家族的五名杂合子女性的研究表明,表达该突变的细胞已从皮肤成纤维细胞培养物中消除,并在不同程度上从造血组织中消除。使用G6PD变体和HPRT基因座处的甲基化模式进行了克隆分析。我们的结果证实了这些家族中的X连锁,并表明对表达对子宫内男性致死的突变的细胞进行选择可能有助于改善携带者女性的有害表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dea/1715454/da30b87b3078/ajhg00111-0106-a.jpg

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