M. Kita et al., DETERMINATION OF INTERFERON-ALPHA-2 ALLELE COMPOSITION IN THE GENOMICDNA FROM HEALTHY-VOLUNTEERS AND LEUKEMIC PATIENTS IN JAPAN, Journal of interferon & cytokine research, 17(3), 1997, pp. 135-140
The three interferon-alpha 2 (IFN-alpha 2) sequences identified to dat
e differ from each other in just two nucleotide positions, both of whi
ch result in changes in amino acids. Thus, the mature IFN-alpha 2a pro
tein product is characterized by a lysine residue at position 23 (AAA)
and a histidine at position 34 (CAA), IFN-alpha 2b has an arginine at
position 23 (AGA) and histidine at position 34 (CAT), and IFN-alpha 2
c has arginine residues at both positions 23 (AGA) and 34 (CGT). These
nucleotide variations in the DNA sequence can be distinguished by sel
ective restriction enzyme analysis. We studied the distributions of th
e three IFN-alpha 2 variants by analyzing chromosomal DNA from 103 Jap
anese volunteers and 33 patients with hematologic disorders. Fragments
of 238 bp and 617 bp of the IFN-alpha 2 gene containing codons 23 and
34 were amplified by PCR using specific primers, and the PCR products
were analyzed with specific restriction nucleases to identify the IFN
-alpha 2 variant sequences. Only IFN-alpha 2b gene was detected in nor
mal volunteers, and no IFN-alpha 2a gene was detected in Japanese subj
ects. However, IFN-alpha 2c was detected in 4 of 33 (12.1%) patients w
ith leukemia.