Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry. Issue 6 (30th May 2020)

• Record Type: Journal Article
• Authors: Lane, William J.; Gleadall, Nicholas S.; Aeschlimann, Judith; Vege, Sunitha; Sanchis‐Juan, Alba; Stephens, Jonathan; Cone Sullivan, Jensyn; Mah, Helen H.; Aguad, Maria; Smeland‐Wagman, Robin; Lebo, Matthew S.; Vijay Kumar, Prathik K.; Kaufman, Richard M.; Green, Robert C.; Ouwehand, Willem H.; Westhoff, Connie M.
• Is Part Of: Transfusion. Volume 60:Issue 6(2020)
• Page Start: 1294
• Page End: 1307
• Publication Date: 2020-05-30
• Subjects: Hematology -- Periodicals; Blood -- Transfusion -- Periodicals; Blood Group Antigens -- Periodicals; Blood Preservation -- Periodicals; Blood Transfusion -- Periodicals; 615
• DOI: 10.1111/trf.15839
• Languages: English
• ISSNs: 0041-1132

Abstract

ABSTRACT: BACKGROUND: The MNS blood group system is defined by three homologous genes: GYPA, GYPB, and GYPE . GYPB encodes for glycophorin B (GPB) carrying S/s and the "universal" antigen U. RBCs of approximately 1% of individuals of African ancestry are U− due to absence of GPB. The U− phenotype has long been attributed to a deletion encompassing GYPB exons 2 to 5 and GYPE exon 1 ( GYPB*01N ). STUDY DESIGN AND METHODS: Samples from two U‐individuals underwent Illumina short read whole genome sequencing (WGS) and Nanopore long read WGS. In addition, two existing WGS datasets, MedSeq (n = 110) and 1000 Genomes (1000G, n = 2535), were analyzed for GYPB deletions. Deletions were confirmed by Sanger sequencing. Twenty known U− donor samples were tested by a PCR assay to determine the specific deletion alleles present in African Americans. RESULTS: Two large GYPB deletions in U− samples of African ancestry were identified: a 110 kb deletion extending left of GYPB (DEL_B_LEFT) and a 103 kb deletion extending right (DEL_B_RIGHT). DEL_B_LEFT and DEL_B_RIGHT were the most common GYPB deletions in the 1000 Genomes Project 669 African genomes (allele frequencies 0.04 and 0.02). Seven additional deletions involving GYPB were seen in African, Admixed American, and South Asian samples. No samples analyzed had GYPB*01N . CONCLUSIONS: The U− phenotype in those of African ancestry is primarily associated with two different complete deletions of GYPB (with intact GYPE ). Seven additional less common GYPB deletion backgrounds were found. GYPB*01N, long assumed to be the allele commonly encoding U− phenotypes, appears to be rare.