Nucleotide sequence of an mRNA transcribed in latent growth-transforming virus infection indicates that it may encode a membrane protein

Publisher Website
Google Scholar
Abstract
The most abundant Epstein-Barr virus mRNA in a latently infected cell line, IB4, established by in vitro growth transformation of human cord blood lymphocytes with virus, was a 2.8-kilobase RNA encoded by largely unique DNA near the right end of the genome. The RNA was transcribed from right to left and 2 introns were spliced out. This region of the genome was sequenced and the exons of the RNA were identified by S1 analysis of DNA-RNA hybrids and primer extension. The first start codon in the RNA was 40 nucleotides from its 5'' end. Beginning with the start codon, there was a 1158-nucleotide open reading frame which crossed both introns. The important characteristics of the translated protein were as follows: the amino terminus was highly charged and not suggestive of a leader sequence; there were 6 markedly hydrophobic .alpha.-helical domains, each having 21 amino acids and connected by 5-7 amino acid segments predicted to be reverse turns; and the carboxy-terminal 200 amino acids were markedly acidic, containing 6 glutamic and 37 aspartic acids. The hydrophobic region is predicted to form 6 membrane-spanning regions, leaving the short charged amino terminus and long acidic carboxy terminus on the inside of the membrane. This protein could be responsible for the new antigen detected in the plasma membrane of Epstein-Barr virus-transformed cells, lymphocyte-determined membrane antigen. There were 2 other open reading frames in the RNA.