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Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.

Irshaid, Nidal M (author)
Eicher, Nicole I (author)
Hustinx, Hein (author)
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Poole, Joyce (author)
Olsson, Martin L (author)
Lund University,Lunds universitet,Avdelningen för hematologi och transfusionsmedicin,Institutionen för laboratoriemedicin,Medicinska fakulteten,Transfusionsmedicin,Forskargrupper vid Lunds universitet,Division of Hematology and Transfusion Medicine,Department of Laboratory Medicine,Faculty of Medicine,Transfusion Medicine,Lund University Research Groups
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 (creator_code:org_t)
2002-02-01
2002
English.
In: British Journal of Haematology. - : Wiley. - 0007-1048. ; 116:2, s. 445-453
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The Kidd (JK) blood group system is of importance in transfusion medicine. The Jk(null) phenotype is associated with absence of the urea transporter in erythrocytes and moderately reduced ability to concentrate urine. We and others recently reported different molecular alterations in the silenced Jkb-like alleles of Polynesians and Finns, populations with higher Jk(null) frequencies. Here we report novel molecular bases of this phenotype in Caucasians. Blood samples from a Swiss and an English family were investigated by serological methods, urea haemolysis test and JK genotyping. Genomic DNA and JK mRNA were sequenced. Genotyping showed homozygosity for Jka-like alleles. The Swiss Jk(null) alleles deviated from wild-type Jka sequence by a nonsense mutation in exon 7 causing an immediate stop codon (Tyr194stop). The English Jk(null) alleles revealed a genomic 1.6 kilobase pair deletion including exons 4 and 5, the former of which includes the translation start codon. Multiple mRNA splicing variants were detected in reticulocytes but exons 3-5 were absent in all transcripts analysed. Screening for these alleles was negative in random donors. Two novel molecular alterations at the JK locus were defined and a multiplex polymerase chain reaction method for detection of the five known silent Jk alleles was developed to complement JK genotyping in clinical transfusion medicine.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Keyword

DNA
Sequence Analysis
RNA
Polymerase Chain Reaction/methods
Membrane Glycoproteins/*metabolism
Phenotype
Kidney Concentrating Ability/*genetics
Kidd Blood-Group System/*genetics
Jordan
Gene Deletion
Human
Messenger/analysis
Erythrocytes/*metabolism
England
Codon
Nonsense
Carrier Proteins/*metabolism
Alleles

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art (subject category)
ref (subject category)

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By the author/editor
Irshaid, Nidal M
Eicher, Nicole I
Hustinx, Hein
Poole, Joyce
Olsson, Martin L
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Hematology
Articles in the publication
British Journal ...
By the university
Lund University

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