Characterization of alternatively spliced transcript variants of glycophorin A and glycophorin B genes in Chinese blood donors. Issue 5 (9th February 2022)

• Record Type: Journal Article
• Authors: Liang, Yanlian; Ren, Jianwei; Zhong, Fuling; Hong, Wenxu; Su, Yuqing; Wu, Fan; Liang, Shuang; Liu, Jun; Fang, Shuanghua; Liang, Yanwen; Fan, Xiuchu; Lin, Jiansuo; Liu, Yi; Feng, Bo; Xu, Yunping
• Is Part Of: Vox sanguinis. Volume 117:Issue 5(2022)
• Page Start: 715
• Page End: 723
• Publication Date: 2022-02-09
• Subjects: alternative RNA splicing -- antigenic diversity -- GYPA mRNA -- GYPB mRNA -- MNS blood group system; Blood -- Periodicals; Blood -- Transfusion -- Periodicals; Immunohematology -- Periodicals; Immunopathology -- Periodicals; 615.39
• DOI: 10.1111/vox.13252
• Languages: English
• ISSNs: 0042-9007

Abstract

Abstract: Background and Objectives: The molecular basis of MNS blood group variants is not fully clear yet. In this study, we have characterized mRNA variants of GYPA and GYPB genes to reveal whether alternative RNA splicing may cause antigenic diversity of the MNS system. Materials and Methods: Total RNA was extracted from peripheral blood of Chinese blood donors and full‐length cDNA products were generated. A nested polymerase chain reaction (PCR)‐based method was established for fragment amplification and Sanger sequencing. Resulted full‐length mRNA sequences were aligned with GYPA or GYPB genomic sequences respectively for exon identification. Amino acid (AA) sequences of GPA and GPB proteins were extrapolated and GYPA‐EGFP, GYPB‐EGFP fusion genes were generated to monitor subcellular distribution of the encoded glycophorin (GP) proteins. Results: Totally 10 blood samples were analysed. GYPB mRNAs of all the subjects demonstrated frequent exon insertion or deletion whereas this kind of variation was only observed in 3 of 10 GYPA mRNA samples. None of the reported Miltenberger hybrids was detected in any of the mRNA samples. The alternative splicing resulted in changes of AA sequences in N‐terminal domains where the MNS antigenic motifs resided; however, subcellular localizations of GP‐EGFP fusion proteins showed that the above‐mentioned AA changes did not affect cell surface distribution of the encoded GP proteins. Conclusions: Alternative RNA splicing may influence the antigenic features of GP proteins but not their cell surface distribution. Therefore, GYPA and GYPB mRNA characterization might be an invaluable supplement to serological phenotyping and DNA‐based genotyping in MNS blood grouping.