Document Detail

Erythroid urea transporter deficiency due to novel JKnull alleles.
MedLine Citation:
PMID:  18028269     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: The Kidd blood group antigens Jka and Jkb are encoded by the red blood cell (RBC) urea transporter gene. Homozygosity for silent JK alleles results in the rare Jk(a-b-) phenotype. To date, seven JKnull alleles have been identified, and of these, two are more frequent in the Polynesians and Finns. This study reports the identification of other JKnull alleles in Jk(a-b-) individuals of different ethnic or geographic origins. STUDY DESIGN AND METHODS: Nine Jk(a-b-) samples and a sample from a Jk(a-b+) mother of a Jk(a+b-) baby were investigated. Polymerase chain reaction amplification and sequence analysis of the JK gene was performed. Western blotting and urea lysis were used to confirm Jk(a-b-) RBCs. RESULTS: Four novel alleles were identified: two different nonsense mutations, 202C>T (Gln68Stop) and 723delA (Ile262Stop) were identified on otherwise consensus JK*1 and JK*2 alleles, respectively. A missense mutation, 956C>T (Thr319Met), was identified in a JK*1 allele from an African-American and a JK*2 allele in two people of subcontinental Indian descent. Immunoblotting and urea lysis confirmed absence of JK glycoprotein in RBC membranes from a sample carrying the 956C>T mutation. Other previously described JKnull mutations were found in samples of origins other than in which they were first identified. CONCLUSION: The molecular bases of the Jk(a-b-) phenotype are diverse and this is the first report of JKnull alleles in individuals of African and subcontinental Indian descent. Although rare, these alleles should be taken into consideration when planning genotyping strategies for blood donors and patients.
Elisabet S Wester; Susan T Johnson; Tama Copeland; Ranjan Malde; Edmond Lee; Jill R Storry; Martin L Olsson
Related Documents :
14742169 - Y-str polymorphisms among five chinese minorities, mosuo, mongolian, naxi, pumi and tib...
17436009 - Forensic efficiency of microsatellites and single nucleotide polymorphisms on the x chr...
15978339 - Forensic evaluation and haplotypes of 19 y-chromosomal str loci in koreans.
6223409 - The canine major histocompatibility complex. population study of dla-d alleles using a ...
7813999 - An investigation of the humvwa31a locus in british caucasians.
15568699 - Specificity of sibship determination using the abi identifiler multiplex system.
7104989 - Karyotype consistency in human colorectal carcinoma cell lines established in vitro.
9216719 - Characterization of chromosome changes in two human prostatic carcinoma cell lines (pc-...
24796499 - X chromosome parental origin and aortic stiffness in turner syndrome.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-11-19
Journal Detail:
Title:  Transfusion     Volume:  48     ISSN:  0041-1132     ISO Abbreviation:  Transfusion     Publication Date:  2008 Feb 
Date Detail:
Created Date:  2008-01-30     Completed Date:  2008-03-28     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0417360     Medline TA:  Transfusion     Country:  United States    
Other Details:
Languages:  eng     Pagination:  365-72     Citation Subset:  IM    
Department of Laboratory Medicine, Division of Hematology and Transfusion Medicine, Lund University and Blood Center, University Hospital, Lund, Sweden.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Base Sequence
Erythroid Cells / metabolism*
Genome, Human / genetics
Introns / genetics
Kidd Blood-Group System / analysis,  chemistry,  genetics*
Membrane Transport Proteins / deficiency*
Mutation / genetics
Reg. No./Substance:
0/Kidd Blood-Group System; 0/Membrane Transport Proteins; 0/urea transporter

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Clinical cardiac involvement in thrombotic thrombocytopenic purpura: a systematic review.
Next Document:  Neonatal alloimmune thrombocytopenia associated with maternal-fetal incompatibility for blood group ...