The O2 allele : Questioning the phenotypic definition of an ABO allele
Yazer, Mark H. and Olsson, Martin L. LU
(2008)
In Immunohematology
24(4).
p.138-147
- Abstract
There are three main alleles in the ABO blood group system, A, B, and O. The former two alleles encode glycosyltransferases resulting in the wild-type A and B phenotypes, whereas the latter allele does not encode a functional enzyme owing to a frameshift polymorphism in the majority of cases. Thus the group O phenotype is the absence of A or B sugars. More than 15 years ago the O 2 allele was described; this allele did not feature the usual crippling 261delG polymorphism, which up to that point was the hallmark of an allele encoding group O, but instead had several other nucleotide polymorphisms that reduced or eliminated the activity of its resulting protein. The classification of this type of allele as encoding group O has... (More)
There are three main alleles in the ABO blood group system, A, B, and O. The former two alleles encode glycosyltransferases resulting in the wild-type A and B phenotypes, whereas the latter allele does not encode a functional enzyme owing to a frameshift polymorphism in the majority of cases. Thus the group O phenotype is the absence of A or B sugars. More than 15 years ago the O 2 allele was described; this allele did not feature the usual crippling 261delG polymorphism, which up to that point was the hallmark of an allele encoding group O, but instead had several other nucleotide polymorphisms that reduced or eliminated the activity of its resulting protein. The classification of this type of allele as encoding group O has been called into question of late as some individuals with an O2 allele appear to have a weak A phenotype. Others with the same allele do not demonstrate any A antigens on their RBCs but might be involved in reverse typing discrepancies. Even within the same pedigree these alleles do not necessarily produce a consistent phenotype. This paper will summarize the detailed biochemical and population-based evidence both for and against the O2 allele's ability to create A antigens or the absence of anti-A in plasma.
(Less)
- author
- Yazer, Mark H.
and Olsson, Martin L.
LU
- organization
- publishing date
- 2008
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- ABO, Allele, Nondeletional, O
- in
- Immunohematology
- volume
- 24
- issue
- 4
- pages
- 10 pages
- publisher
- American Red Cross
- external identifiers
-
- pmid:19856716
- scopus:62849113366
- ISSN
- 0894-203X
- DOI
- 10.21307/immunohematology-2019-288
- language
- English
- LU publication?
- yes
- additional info
- Copyright: Copyright 2009 Elsevier B.V., All rights reserved.
- id
- 7de617aa-7db4-4b00-9d84-d800c8e94945
- date added to LUP
- 2021-08-04 12:54:38
- date last changed
- 2024-01-05 13:51:59
@article{7de617aa-7db4-4b00-9d84-d800c8e94945,
abstract = {{<p>There are three main alleles in the ABO blood group system, A, B, and O. The former two alleles encode glycosyltransferases resulting in the wild-type A and B phenotypes, whereas the latter allele does not encode a functional enzyme owing to a frameshift polymorphism in the majority of cases. Thus the group O phenotype is the absence of A or B sugars. More than 15 years ago the O <sup>2</sup> allele was described; this allele did not feature the usual crippling 261delG polymorphism, which up to that point was the hallmark of an allele encoding group O, but instead had several other nucleotide polymorphisms that reduced or eliminated the activity of its resulting protein. The classification of this type of allele as encoding group O has been called into question of late as some individuals with an O2 allele appear to have a weak A phenotype. Others with the same allele do not demonstrate any A antigens on their RBCs but might be involved in reverse typing discrepancies. Even within the same pedigree these alleles do not necessarily produce a consistent phenotype. This paper will summarize the detailed biochemical and population-based evidence both for and against the O<sup>2</sup> allele's ability to create A antigens or the absence of anti-A in plasma.</p>}},
author = {{Yazer, Mark H. and Olsson, Martin L.}},
issn = {{0894-203X}},
keywords = {{ABO; Allele; Nondeletional; O}},
language = {{eng}},
number = {{4}},
pages = {{138--147}},
publisher = {{American Red Cross}},
series = {{Immunohematology}},
title = {{The O<sup>2</sup> allele : Questioning the phenotypic definition of an ABO allele}},
url = {{http://dx.doi.org/10.21307/immunohematology-2019-288}},
doi = {{10.21307/immunohematology-2019-288}},
volume = {{24}},
year = {{2008}},
}