InventorsApplicationNo. 06/614350 filed on 05/25/1984US Classes:435/320.1, VECTOR, PER SE (E.G., PLASMID, HYBRID PLASMID, COSMID, VIRAL VECTOR, BACTERIOPHAGE VECTOR, ETC.) BACTERIOPHAGE VECTOR, ETC.)435/6, Involving nucleic acid435/91.3, Polynucleotide contains only ribonucleotide monomers536/23.1, DNA or RNA fragments or modified forms thereof (e.g., genes, etc.)536/24.1, Non-coding sequences which control transcription or translation processes (e.g., promoters, operators, enhancers, ribosome binding sites, etc.)536/24.3, Probes for detection of specific nucleotide sequences or primers for the synthesis of DNA or RNA536/25.1, 3`-5` linked RNA536/25.32Labels or markers utilized (e.g., radiotracer, affinity, fluoroescent, phosphorescent, markers, etc.)ExaminersPrimary: Wiseman, Thomas G.Assistant: Seidman, S. Attorney, Agent or FirmInternational ClassesC12P 19/00 (20060101)C12P 19/34 (20060101) C12Q 1/68 (20060101) C12N 15/10 (20060101) AbstractThis invention concerns recombinant RNA molecules comprising a recognition sequence for the binding of an RNA-directed RNA polymerase, a sequence for the initiation of product strand synthesis and a heterologous sequence of interest inserted at a specific site in the internal region of the recombinant molecule. Such recombinant RNA molecules are capable of serving as a template for the synthesis of complementary single-stranded molecules by RNA-directed RNA polymerase. The product molecules so formed are also capable of serving as a template for the synthesis of additional copies of the original recombinant RNA molecule. In a preferred embodiment of the invention Qଲ replicase is used as the RNA-directed RNA polymerase.Other References
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