Nucleic acid sequence amplification method, composition and kit

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

435 6, 435 9151, 435 9153, 536 2432, 536 2433, 935 17, 935 18, 935 8, 935 78, C12P 1934, C12Q 168, C07H 2104

Patent

active

055545165

ABSTRACT:
A method, composition and kit for amplifying a target nucleic acid sequence under conditions of substantially constant temperature, ionic strength, and pH and using only a single promoter-primer. To effect the amplification, a supply of a single promoter-primer having a promoter and a primer complementary to the 3'-end of the target sequence, and a reverse transcriptase and an RNA polymerase are provided to a mixture including the target sequence; the amplification proceeds accordingly. The invention is useful for generating copies of a nucleic acid target sequence for purposes that include assays to quantitate specific nucleic acid sequences in clinical, environmental, forensic and similar samples, cloning and generating probes.

REFERENCES:
patent: 4683202 (1987-07-01), Mullis
patent: 4876187 (1989-10-01), Duck et al.
patent: 5030557 (1991-07-01), Hogan et al.
Gingeras et al., U.S. patent application Ser. No. 07/202,978 filed Jun. 6, 1988, "Transcription-Based Nucleic Acid Amplification/Detection Systems".
Joyce, "Amplification, mutation and selection of catalytic RNA", Gene, 82:83-87, 1989.
Lowary et al., "A Better Way to Make RNA for Physical Studies", Knippenberg, eds. Structure & Dynamics of RNA, Nato ASI Series, vol. 110, New York, Plenum Press (1986).
Murakawa et al., "Direct Detection of HIV-1 RNA from AIDS and ARC Patient Samples," DNA, 7:287-295, 1988.
Mullis et al., "Specific Synthesis of DNA in Vitro via a Polymerase-Catalyzed Chain Reaction", Methods in Enzymology, 155:355, 1987.
Watson et al., "Molecular Structure of Nucleic Acids", Nature, Apr. 25, 1953, p. 737.
Khorana, "Total Synthesis of a Gene", Science 203:614, 1979.
Okayama et al., "High-Efficiency Cloning of Full-Length cDNA", Molecular and Cellular Biology 2:161-170, 1982.
Watson et al., "Genetical Implications of the Structure of Deoxyribonucleic Acid", Nature, 171:964, 1953.
Stent, "Molecular Biology of Bacterial Viruses", W. H. Freeman & Company, 1963.
Hayes, "The Genetics of Bacteria and their Viruses", John Wiley & Sons In.c, New York, Blackwell Scientific Publications 1964, 1968.
Lomonossoff et al., "The location of the first AUG codons in Cowpea mosaic virus RNAs", Nucleic Acids Research 10:4861, 1982.
Cashdollar et al., "Cloning the double-stranded RNA genes ofo reovirus: Sequence of the cloned S2 gene", Proc. Natl. Acad. Sci. USA 79:7644-7648, 1982.
Both et al., "A general strategy for cloning double-stranded RNA: nucleotide sequence of the Simian-11 rotavirus gene 8", Nucleic Acids Research 10:7075, 1982.
Kupper et al., "Promoter dependent transcription of TRNA.sub.1.sup.Tyr genes using DNA fragments produced by restriction enzymes", Proc. Natl. Acad. Sci. USA 72:4754, 1975.
Rossi et al., "An Alternate Method for Synthesis of Double-Stranded DNA Segments", J. Biol. Chem. 257:9226, 1982.
Zoller et al., "Oligonucleotide-Directed Mutagenesis of DNA Fragments Cloned into M13 Vectors", Methods in Enzymology, 100:468, 1983.
Guatelli et al., "Isothermal, in vitro amplification of nucleic acids by a multienzyme reaction modeled after retroviral replication", Proc. Natl. Acad. Sci. USA 87:1874, 1990.
European search report for Application No. 90307503.4 dated Jul. 12, 1991 (EP 0 408 295 A2).
Kwoh et al., "Transcription-based amplification system and detection of amplified human immunodeficiency virus type 1 with a bead-based sandwich hybridization format", Proc. Natl. Acad. Sci. USA 86:1173-1177, 1989.
Krug and Berger, "Ribonuclease H activities associated with viral reverse transcriptases are endocucleases", Proc. Natl. Acad. Sci. USA 86:3539-3543, 1989.
Oyama et al., "Intrinsic Properties of Reverse Transcriptase in Reverse Transcription", J. Biol. Chem. 264:18808-18817, 1989.
Grachev et al., "Oligonucleotides complementary to a promoter over the region -8 . . . +2 as transcription primers for E. coli RNA polymerase", Nucleic Acids Research 12:8501, 1984.
Milligan et al., "Oligonucleotide synthesis using T7 RNA polymerase and synthetic DNA templates", Nucleic Acids Research 15:8783, 1987.
Gubler, "[35] Second-Strand cDNA Synthesis: mRNA Fragments as Primers", Methods in Enzymology 152:330-335, 1987.
Krug & Berger, "Guide to Molecular Cloning Techniques"; Methods in Enzymology, Academic Press, NY NY, 152:316-325.
Bethesda Research Laboratoris Catalogue and Reference Guide (1988) Bethesda Research Laboratories, Bethesda MD, p. 37.
Cox et al., "The 16S ribosomal RNA of Mycobacterium leprae contains a unique sequence which can be used for identification by the polymerase chain reaction", 35:284-290, 1991.
Tayagi et al., "Molecular Biology--Transfer RNA genes in mycobacteria: organization and molecular cloning", Trop. Med. Parasitol, 41:294-296, 1990.
Walker et al., "Isothermal in vitro amplification of DNA by a restriction enzyme/DNA polymerase system", Proc. Natl. Acad. Sci. USA 89:392-396, 1992.
Hentosh et al., "Polymerase Chain Reaction Amplification of Single-Stranded DNA Containing a Base Analog, 2-Chloroadenine", Analytical Biochemistry, 201:277-281, 1992.
Wilk et al., "Backbone-modified oligonucleotides containing a butanediol-1,3 moiety as a `vicarious segment` for the deoxyribosyl moiety--synthesis and enzyme studies", Nucleic Acids Research, 18:2065-2068, 1990.
Bochmjer Mannheim Catalog, 1990/1991, pp. 69-70.
Rogers et al, Proc Natl Acad Sci USA (1985) 82: 1160-1164.
Fahy et al PCR Methods and Applications (Aug. 1991) 1: 25-33.
Kwoh et al American Biotechnology Laboratory (1990) 18; 14-25.
Sorge et al. Proc Natl Acad Sci (1989) 86: 9208-9212.
Hogan et al. GenBank Accession No. N80793 Nov. 30, 1990.
Grachev et al Nucl Acids Res (1984) 12: 8509-8524.
Davis et al J Clin Micro (1991) 29: 2193-2196.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Nucleic acid sequence amplification method, composition and kit does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Nucleic acid sequence amplification method, composition and kit, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Nucleic acid sequence amplification method, composition and kit will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-1319865

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.