Pedigree analysis for the rare RHD DVa allele: serological and molecular studies

Jing-Jing Gao, Xiongpeng Zhu, Jinzhe Tan, Mingquan Wang, Wen-qian Xu, Jhy Sheng Chang
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Abstract

Until now, worldwide more than 80 different alleles producing weak D phenotypes have been identified. Here we identified rare RHD DVa alleles in Chinese individuals associated with weak expression of D antigen and an RHD phenotype resembling DVI. Multi-monoclonal anti-D antibodies were used to identify the RHD phenotyping for rare RHD DVa. RHD genotyping was used to confirm the presence of RHD exons and identify RHD, RHCE hybrids and exon deficiencies. Sanger sequencing was used to identify nucleotide polymorphisms in RHD exons. Pedigree analysis demonstrated RHD DVa allele alterations of 667 T>G, 676 G>C, 697 G>C, 712 G>A, 733 G>C, 744 C>T and 1227 G>A, which means the proband's alleles were RHD DVa-3 [also called RHD-CE(5)-D] and 1227 G>A. The results also demonstrated RHD DVa and the original RHD Va allele without 1227 G>A. The study suggests that RHD phenotyping is a superior strategy for the molecular analysis of RHD variant in Chinese subjects, and for understanding related polymorphisms and mutations.
罕见RHD DVa等位基因的家系分析:血清学和分子研究
到目前为止,全世界已经鉴定出80多种产生弱D表型的不同等位基因。在这里,我们在中国个体中发现了与D抗原弱表达和类似DVI的RHD表型相关的罕见RHD DVa等位基因。采用多单克隆抗d抗体对罕见的RHD DVa进行表型鉴定。RHD基因分型用于确认RHD外显子的存在,并鉴定RHD、RHCE杂交和外显子缺陷。Sanger测序用于鉴定RHD外显子的核苷酸多态性。家谱分析显示,RHD DVa等位基因变异为667 T>G、676 G>C、697 G>C、712 G>A、733 G>C、744 C>T和1227 G>A,即先证者的等位基因为RHD DVa-3[又称RHD- ce (5)-D]和1227 G>A。RHD DVa和原RHD Va等位基因均无1227 G>A。研究结果表明,RHD表型分析是分析中国人RHD变异、了解相关多态性和突变的优越策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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