Suppr超能文献

血色素沉着病基因定位于靠近D6S105处。

Localization of the hemochromatosis gene close to D6S105.

作者信息

Jazwinska E C, Lee S C, Webb S I, Halliday J W, Powell L W

机构信息

Liver Unit, Queensland Institute of Medical Research, Royal Brisbane Hospital, Herston, Australia.

出版信息

Am J Hum Genet. 1993 Aug;53(2):347-52.

Abstract

The hemochromatosis (HC) gene is known to be linked to HLA-A (6p21.3); however, its precise location has been difficult to determine because of a lack of additional highly polymorphic markers for this region. The recent identification of short tandem repeat sequences (microsatellites) has now provided this area with a number of markers with similar polymorphic index to the HLA serological polymorphisms. Using four microsatellites--D6S105, D6S109, D6S89, and F13A--together with the HLA class I loci HLA-A and HLA-B in 13 large pedigrees clearly segregating for HC, we have been able to refine the location of the HC gene. We identified no recombination between HC and HLA-A or D6S105, and two-point analyses placed the HC gene within one centimorgan (cM) of HLA-A and D6S105 (HLA-A maximum of the lod score [Zmax] of 9.90 at recombination fraction [theta] of 0.0, and D6S105 Zmax of 8.26 at theta of 0.0). The markers HLA-B, D6S109, D6S89, and F13A were separated from the HC locus by recombination, defining the centromeric and telomeric limits for the HC gene as HLA-B and D6S109, respectively. A multipoint map constructed using HLA-B, HLA-A, and D6S109 indicates that the HC gene is located in a region less than 1 cM proximal to HLA-A and less than 1 cM telomeric of HLA-A. These pedigree data indicate an association between HC and specific alleles at HLA-A and D6S105 (i.e., HLA-A3 and D6S105 allele 8).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已知血色素沉着症(HC)基因与HLA - A(6p21.3)相关联;然而,由于该区域缺乏其他高度多态性标记,其精确位置一直难以确定。最近短串联重复序列(微卫星)的鉴定为该区域提供了一些与HLA血清学多态性具有相似多态性指数的标记。在13个明确显示HC分离的大家系中,使用四个微卫星——D6S105、D6S109、D6S89和F13A——以及HLA I类基因座HLA - A和HLA - B,我们得以精确确定HC基因的位置。我们发现HC与HLA - A或D6S105之间没有重组,两点分析将HC基因定位在距HLA - A和D6S105一厘摩(cM)范围内(HLA - A在重组率[θ]为0.0时最大连锁值[Zmax]为9.90,D6S105在θ为0.0时Zmax为8.26)。标记HLA - B、D6S109、D6S89和F13A通过重组与HC基因座分离,分别将HC基因的着丝粒和端粒界限定义为HLA - B和D6S109。使用HLA - B、HLA - A和D6S109构建的多点图谱表明,HC基因位于距HLA - A近端小于1 cM且距HLA - A端粒小于1 cM的区域。这些家系数据表明HC与HLA - A和D6S105的特定等位基因(即HLA - A3和D6S105等位基因8)之间存在关联。(摘要截短于250字)

相似文献

引用本文的文献

2
Disorders of metal metabolism.金属代谢紊乱
Transl Sci Rare Dis. 2017 Dec 18;2(3-4):101-139. doi: 10.3233/TRD-170015.

本文引用的文献

1
Strategies for multilocus linkage analysis in humans.人类多位点连锁分析策略。
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3443-6. doi: 10.1073/pnas.81.11.3443.
7
Report of the committee on linkage and gene order.
Cytogenet Cell Genet. 1989;51(1-4):459-502. doi: 10.1159/000132805.
9
Dinucleotide repeat polymorphism at the D6S89 locus.D6S89位点的二核苷酸重复多态性。
Nucleic Acids Res. 1990 Jul 25;18(14):4301. doi: 10.1093/nar/18.14.4301.

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