Document 0422 DOCN M9590422 TI Expression and characterization of proteins produced by mRNAs spliced into the X region of the human T-cell leukemia/lymphotropic virus type II. DT 9509 AU Ciminale V; D'Agostino DM; Zotti L; Franchini G; Felber BK; Chieco-Bianchi L; Institute of Oncology, University of Padova, Italy. SO Virology. 1995 Jun 1;209(2):445-56. Unique Identifier : AIDSLINE GENBANK/L41677 AB In previous studies we showed that human T-cell leukemia/lymphotropic virus type I (HTLV-I) may produce novel proteins encoded in the X region. To investigate a possible correlation between expression of viral genes and different biologic properties of HTLV-I and HTLV-II, we analyzed expression of HTLV-II in the chronically infected cell line MoT. Reverse transcription-polymerase chain reaction analyses revealed that the virus produces several mRNAs singly or doubly spliced into the X region. Corresponding cDNAs were cloned and transfected into a HeLa cell line; resulting proteins were designated according to their sizes and coding open reading frames (ORFs). p10xI and p11xV were produced by a dicistronic doubly spliced mRNA. p10xI was generated by translation of the first exon of rex linked to the x-I ORF; p11xV was translated from the tax initiation codon linked to the x-V ORF. Two singly spliced polycistronic mRNAs produced p28xII, coded by the x-II ORF, and several isoforms generated by initiation within the x-III ORF. Studies of the proteins' subcellular localization revealed that they exhibited distinct targeting patterns. Comparison of these proteins with their HTLV-I counterparts indicated intriguing differences between these two viruses, suggesting that further study of the X region products may aid in defining genetic determinants of pathogenicity. DE *Alternative Splicing Amino Acid Sequence Antigenic Determinants/ANALYSIS Base Sequence Cell Line Comparative Study DNA Primers Genes, env Genes, gag Genes, pol Genome, Viral Human HTLV-I/GENETICS/METABOLISM HTLV-II/GENETICS/*METABOLISM Molecular Sequence Data Open Reading Frames Recombinant Proteins/ANALYSIS/BIOSYNTHESIS RNA, Messenger/*METABOLISM Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. Transfection Viral Proteins/*BIOSYNTHESIS JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).