Discovery of two novel variants of KIR2DS5 reveals this gene to be a common component of human KIR 'B' haplotypes

Citation
C. Vilches et al., Discovery of two novel variants of KIR2DS5 reveals this gene to be a common component of human KIR 'B' haplotypes, TISSUE ANTI, 56(5), 2000, pp. 453-456
Citations number
10
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TISSUE ANTIGENS
ISSN journal
00012815 → ACNP
Volume
56
Issue
5
Year of publication
2000
Pages
453 - 456
Database
ISI
SICI code
0001-2815(200011)56:5<453:DOTNVO>2.0.ZU;2-X
Abstract
The gene encoding the non-inhibitory receptor KIR2DS5 has so far been repre sented by a single cDNA sequence, NKAT9. A previous study by polymerase cha in reaction using sequence-specific primers (PCR-SSP) failed to detect NKAT 9 in genomic DNA of 52 donors, which suggested that KIR2DS5 could be a rare gene. Here, we have characterized two novel variants of KIR2DS5 that diffe r from NKAT9 by 8 and 10 nucleotide substitutions. The frequency of KIR2DS5 was then re-assessed by PCR-SSP using primers specific for conserved seque nces of all three known KIR2DS5 variants. We found KIR2DS5 is not a rare ge ne, but one present in 26% of 34 donors representing the major ethnic group s. Like other non-inhibitory KIR, the distribution of KIR2DS5 is restricted to the 'B' subset of KIR-gene haplotypes. Transcription of the KIR2DS5 gen e was studied by reverse transcriptase (RT)-PCR in natural killer (NK) cell s from one donor and shown to follow the clonal distribution seen for most other KIR genes.