与新型ABO*A等位基因变异c.106delinsGGGG相关的A弱表型
Sanmukh Ratilal Joshi1, Glenda Millard2, Mayuri Vekariya1
1Lok Samarpan Raktadan Kendra and Research Center, Surat, Gujarat, India.
Asian journal of transfusion science
|July 22, 2024
概括
在6名具有弱A抗原表型的健康捐赠者中发现了一种新的ABO*A基因 (c.106delinsGG). 这种遗传变异解释了观察到的血型分类差异,并对输血医学有影响.
科学领域:
- 遗传学 遗传学 是一个
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
背景情况:
- 在前向和反向的ABO血液分组中存在差异,可能是由于ABO等位基因的遗传变异引起的.
- 研究具有弱A抗原的健康捐赠者对于了解ABO血型变异至关重要.
研究的目的:
- 在健康的献血者中确定负责弱A抗原表型的特定等位基因.
- 描述 ABO 血型差异的遗传基础.
主要方法:
- 标准的血清学方法被用于最初的血液分组.
- 使用定制探针面板和Illumina MiSeq.进行了DNA分子测序.
- 用于变异分析的QIAGEN CLC基因组学工作台.
主要成果:
- 六个健康的捐赠者表现出一个弱的A抗原表型 (Aweak) 与混合场聚合.
- 血清学和家族研究证实了Aend表型及其遗传性.
- 分子分析揭示了一种新的ABO*A等位基因变异,c.106delinsGG,与弱A表型相关.
结论:
- 一个新的ABO*A等位基因 (c.106delinsGG) 与六个个体的Aweak表型有关.
- 这种新发现的等位基因和表型尚未在国际输血协会数据库中列出.
- 在UCSC基因组浏览器 (rs782544248) 中记录了c.106delinsGG变异.
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