Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3350947 | Human Immunology | 2012 | 7 Pages |
Abstract
Genomic DNA, extracted from 20 KIR2DS2/4+ donor and recipient cells, was treated with sodium bisulfate that will modify the unmethylated cytosine into uracil. Sequencing chromatographs were examined for C/T double peak indicative of base conversion. A CpG island in KIR2DS2 promoter spans from â160 to +26 with six cytosine sites. In contrast, the KIR2DS4 promoter CpG island contains three cytosine sites. The noted increase of unmethylated sites was associated with increased KIR expression as measured by mRNA-cDNA Q-PCR. In addition, the frequency of unmethylated sites in the CpG island was increased after HCT. The mechanism through which hypomethylation occurs after HCT is not known but it suggests a linkage to NK clonal expansion during the process of NK education in response to transplant therapy or viral infection.
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Authors
Ghislaine M. Gallez-Hawkins, Xiuli Li, Anne E. Franck, Ketevan Gendzekhadze, Ryotaro Nakamura, Stephen J. Forman, David Senitzer, John A. Zaia,