Document 0212 DOCN M94A0212 TI Characterization of a kissing hairpin complex derived from the human immunodeficiency virus genome. DT 9412 AU Chang KY; Tinoco I Jr; Department of Chemistry, University of California, Berkeley; 94720. SO Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8705-9. Unique Identifier : AIDSLINE MED/94360000 AB Base-pair formation between two hairpin loops--a kissing complex--is an RNA-folding motif that links two elements of RNA secondary structure. It is also a unique protein recognition site involved in regulation of ColE1 plasmid DNA replication. The trans-activation response element (TAR), a hairpin and bulge at the 5' end of the untranslated leader region of the human immunodeficiency virus 1 mRNA, enhances the transcription of the virus and is necessary for viral replication. Gel electrophoresis and absorbance melting curves indicate that a synthesized RNA hairpin (Tar*-16) with a loop sequence complementary to the TAR loop sequence (CUGGGA) associates specifically with a 16-nucleotide TAR hairpin (Tar-16) to form a stable complex. RNase T1 probing indicates that the three guanines in the Tar-16 loop become inaccessible in the complex. NMR imino proton spectra reveal that 5 base pairs are formed between the two hairpin loops (Tar-16 and Tar*-16); only the adenine at the 3' terminus of the TAR loop does not form a base pair with the 5'-terminal uracil of the complementary loop. A 14-nucleotide hairpin [CCUA(UCCCAG)UAGG] with a loop sequence complementary to the TAR loop is conserved within the gag gene of human immunodeficiency virus 1. A synthesized RNA hairpin corresponding to this conserved sequence also binds to the Tar-16 hairpin with high affinity. It is possible that the same RNA loop-loop interaction occurs during the viral life cycle. DE Base Sequence Hydrogen Bonding HIV-1/*ULTRASTRUCTURE Molecular Sequence Data Nuclear Magnetic Resonance Nucleic Acid Conformation Regulatory Sequences, Nucleic Acid RNA, Viral/*ULTRASTRUCTURE Support, U.S. Gov't, Non-P.H.S. Support, U.S. Gov't, P.H.S. JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).