ABSTRACT
We describe the molecular cloning of a serogroup 2 simian retrovirus (SRV; D2/RHE/OR) and present the sequence of its envelope (env) glycoprotein gene and 3' long terminal repeat region. This report documents the first infectious molecular clone of a serogroup 2 SRV and provides env sequence verification of genetic diversity among serogroup 2 SRV isolates.
Subject(s)
Gene Products, env/genetics , Repetitive Sequences, Nucleic Acid , Retroviruses, Simian/genetics , Simian Acquired Immunodeficiency Syndrome/virology , Amino Acid Sequence , Animals , Base Sequence , Cell Line , Cloning, Molecular , DNA, Viral , Molecular Sequence Data , Retroviruses, Simian/classification , Retroviruses, Simian/pathogenicity , Retroviruses, Simian/physiology , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid , Serotyping , Transfection , Virulence/geneticsABSTRACT
Genetic, biochemical, and biophysical studies have begun to reveal details of the structures of Arc and Mnt and show that these repressors use residues at their N-terminal ends for operator recognition and binding. Some of the DNA contacts made by these residues have been identified, and this information together with NMR studies has permitted the construction of models of the DNA binding region. Although the accuracy of these models remains to be determined, it seems clear that Arc and Mnt are members of a new class of DNA-binding proteins.
Subject(s)
DNA-Binding Proteins , Operator Regions, Genetic , Repressor Proteins , Transcription Factors , Amino Acid Sequence , Coliphages/genetics , DNA-Binding Proteins/ultrastructure , Hydrogen Bonding , Macromolecular Substances , Molecular Sequence Data , Protein Binding , Protein Conformation , Repressor Proteins/ultrastructure , Structure-Activity Relationship , Transcription Factors/ultrastructureABSTRACT
A set of arc operators with transition and/or transversion mutations at each operator base pair has been constructed. By determining the ability of Arc to bind these variant operators, the importance of each base pair for Arc recognition has been assessed. Methylation protection experiments have also been used to probe points of close contact between Arc and most of the mutant operators. These data, together with phosphate interference results obtained previously for the wild type operator, provide information about the operator surface that is contacted when Arc binds.