Document 3172 DOCN M94A3172 TI Expression of HTLV-I rex and tax recombinant proteins in E. coli. DT 9412 AU Susova O; Pavlish O; Scherbak L; Gurtsevitch V; Cancer Research Center, Moscow, Russia. SO Int Conf AIDS. 1994 Aug 7-12;10(1):137 (abstract no. PA0167). Unique Identifier : AIDSLINE ICA10/94369403 AB OBJECTIVE: HTLV-I has been known to contain specific regulatory genes rex and tax. The aim of the investigation was to obtain and to characterize recombinant proteins encoded by these genes in bacterial cells. METHODS: Routine gene-engeneering and biotechnological procedures were used to accomplish molecular cloning for above purposes. Several kind of expressing vectors were used including pATH, pEX as well as pMAL-c and pMAL-p which were described elsewhere. RESULTS: pMAL-c-derived plasmid clone expressing C-terminal part of p40-tax (167 aa residues) turned out to be the most perspective for both to generate anti-tax rabbit polyclonal antibodies and to detect tax-specific antibodies in human sera. Recombinant p21-rex hybrid protein which has been expressed in pATH-vector system was low immunogenic and incapable to detect rex-specific antibodies in human sera of HTLV-I carriers. However, rabbit antiserum obtained against mentioned recombinant protein was able to detect p21 cellular protein in HTLV-I-containing cell lines (C 91/PL, MT-2, HVT-102). CONCLUSIONS: A new plasmid DNAs expressing HTLV-I recombinant tax and rex proteins and generating appropriate polyclonal anti-sera have been obtained. Immunoblot analysis allowed us to demonstrate a moderate immune response to p40-tax in some cases with no antibodies to HTLV-I structural proteins. DE Cloning, Molecular/METHODS DNA, Viral/METABOLISM Gene Products, rex/*BIOSYNTHESIS Gene Products, tax/*BIOSYNTHESIS Genes, pX Genetic Vectors HTLV-I/GENETICS/*METABOLISM Plasmids Recombinant Proteins/*BIOSYNTHESIS MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).