PRIMARY STRUCTURE OF NONHISTONE CHROMOSOMAL PROTEIN HMG2 REVEALED BY THE NUCLEOTIDE-SEQUENCE

The isolation and sequencing of a cDNA clone for the entire sequence of pig thymus non-histone protein HMG2 are described. cDNA the size of 1153 nucleotides contains an open reading frame of 627 nucleotides. The 5′-untranslated region of 146 nucleotides is extremely rich in GC residues whereas the 3′-untranslated region of 380 nucleotides is rich in AT residues. The open reading frame encodes 209 amino acids, which contain a unique continuous run of 23 acidic amino acids at the C-terminal. The deduced amino acid sequence is 79% homologous to that of HMG1 protein from the same source which we reported [Tsuda, K., Kikuchi, M, Mori, K., Waga, S., & Yoshida, M. (1988) Biochemistry 27, 6159–6163]. In addition, the hydropathy index profiles of both proteins are very similar, supporting that they have similar structural features. Northern analysis of poly(A+) RNA reveals that a single-sized mRNA codes for HMG2 protein. Southern analysis suggests that the HMG2 coding gene is homogeneous within the pig thymus genome. © 1990, American Chemical Society. All rights reserved.