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Cloning and expression of the human myeloid cell nuclear differentiation antigen: Regulation by interferon α
Author(s) -
Briggs J. A.,
Burrus G. R.,
Stickney B. D.,
Briggs Robert C.
Publication year - 1992
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.240490114
Subject(s) - biology , microbiology and biotechnology , complementary dna , expressed sequence tag , gene , genetics
Abstract The human myeloid cell nuclear differentiation antigen (MNDA) is a protein of 406 amino acids that is expressed specifically in granulocytes, monocytes and earlier stage cells of these lineages. Degenerate oligonucleotides that could encode regions of MNDA amino acid sequence were used to amplify the MNDA cDNA sequence using the polymerase chain reaction. The amplified cDNA product wsa sequenced to confirm that it encoded the MNDA protein. It was then used as a probe to isolate five clones from a human bone marrow λgt10 cDNA library. A clone containing a 1,672 base pair cDNA insert was sequenced and found to encode the entire MNDA open reading frame, as well as 5′ and 3′ untranslated regions. The primary structure of the MNDA contains extensive regions of sequence similarity with the protein products of the interferon‐inducible genes: 204 and interferon regulatory factor 2. In addition, a 12‐base sequence matching the interferon‐stimulated response element consensus sequence [GAAAN(N)GAAA] is located in the 5′ untranslated region of the MNDA cDNA. The 1.8 kb MNDA mRNA was detected only in cells that express the antigen and the level of MNDA mRNA was elevated in cells treated with either recombinant or natural interferon α. The MNDA mRNA was not induced by interferon α in cells that do not exhibit a constitutive level of the MNDA mRNA. The MNDA contains sequence motifs found in gene regulatory proteins. The expression and the primary structure of the MNDA indicates that it plays a role in the granulocyte/monocyte cell‐specific response to interferon.