Suppr超能文献

BCR基因的CGG重复多态性排除了导致费城染色体的易感等位基因。

CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome.

作者信息

Riggins G J, Sherman S L, Phillips C N, Stock W, Westbrook C A, Warren S T

机构信息

Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

Genes Chromosomes Cancer. 1994 Feb;9(2):141-4. doi: 10.1002/gcc.2870090211.

Abstract

The Philadelphia chromosome (Ph) is associated with leukemia, most frequently of the chronic myelogenous variety. The Ph chromosome is a translocation chromosome which gains oncogenic potential through the fusion of the ABL oncogene of chromosome 9 with the BCR gene of chromosome 22. The Ph is believed to arise from random chromosome rearrangement with a subsequent selective advantage of the malignant cell line. However, alleles may be present in the population which predispose toward this specific rearrangement. We used a highly polymorphic CGG-repeat polymorphism within the first exon of the BCR gene to determine BCR allele frequencies among 26 leukemia patients with the Ph chromosome and 63 control individuals. Eight BCR alleles of variable CGG-repeat length were present in both groups at statistically similar frequencies and in Hardy-Weinberg equilibrium. We therefore concluded that there are no alleles of the BCR gene that have a major predisposing influence on the development of the Ph chromosome and subsequent leukemia.

摘要

费城染色体(Ph)与白血病相关,最常见于慢性粒细胞白血病。Ph染色体是一种易位染色体,它通过9号染色体上的ABL癌基因与22号染色体上的BCR基因融合而获得致癌潜能。据信Ph染色体源于随机的染色体重排,随后恶性细胞系具有选择性优势。然而,人群中可能存在易导致这种特定重排的等位基因。我们利用BCR基因第一外显子内高度多态的CGG重复多态性,来确定26例有Ph染色体的白血病患者和63例对照个体中的BCR等位基因频率。两组中均存在8种CGG重复长度可变的BCR等位基因,其频率在统计学上相似且处于哈迪-温伯格平衡。因此,我们得出结论,BCR基因不存在对Ph染色体及后续白血病发展有主要易患影响的等位基因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验