Back to Search Start Over

ACKR1 Alleles at 5.6 kb in a Well-Characterized Renewable US Food and Drug Administration (FDA) Reference Panel for Standardization of Blood Group Genotyping.

Authors :
Srivastava K
Khil PP
Sippert E
Volkova E
Dekker JP
Rios M
Flegel WA
Source :
The Journal of molecular diagnostics : JMD [J Mol Diagn] 2020 Oct; Vol. 22 (10), pp. 1272-1279. Date of Electronic Publication: 2020 Jul 17.
Publication Year :
2020

Abstract

The glycoprotein encoded by the ACKR1 gene expresses the Duffy blood group antigens and is a receptor for malaria parasites. We recently described 18 long-range ACKR1 alleles in an autochthonous population of a malaria endemic region. Extending this work, we sequenced the gene in a 53-sample repository established by the US Food and Drug Administration (FDA) as reference reagents for blood group genotyping. The FDA samples have been characterized for 19 genes; however, long-range haplotype information for these genes, including ACKR1, was lacking. We used a hybrid approach, novel for this type of gene, to characterize ACKR1 by combining two next-generation sequencing technologies, the short-read massively parallel sequencing and the long-read nanopore sequencing. The expedient integration of data from both next-generation sequencing systems were necessary and sufficient to allow determination of all 25 long-range ACKR1 alleles found in the 53 samples accurately. All 25 alleles identified in our current FDA cohort were novel and, unexpectedly, none had been observed among the 18 alleles in our previous study. The alleles will be useful for validation, calibration, and proficiency testing of red cell genotyping. The lack of any overlap between the ACKR1 alleles in the two studies documents differences in mutation rate and recombination frequency among populations. The exact haplotype and their interethnic or interpopulation dissimilarities can influence disease susceptibility and therapy.<br /> (Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1943-7811
Volume :
22
Issue :
10
Database :
MEDLINE
Journal :
The Journal of molecular diagnostics : JMD
Publication Type :
Academic Journal
Accession number :
32688055
Full Text :
https://doi.org/10.1016/j.jmoldx.2020.06.014