Expression of SV40 and polyoma T antigens in E. coli. 1983

T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
Sidney Farber Cancer Institute, Laboratory of Neoplastic Disease Mechanisms, Boston, Massachusetts 02115.

UI MeSH Term Description Entries
D010957 Plasmids Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS. Episomes,Episome,Plasmid
D011401 Promoter Regions, Genetic DNA sequences which are recognized (directly or indirectly) and bound by a DNA-dependent RNA polymerase during the initiation of transcription. Highly conserved sequences within the promoter include the Pribnow box in bacteria and the TATA BOX in eukaryotes. rRNA Promoter,Early Promoters, Genetic,Late Promoters, Genetic,Middle Promoters, Genetic,Promoter Regions,Promoter, Genetic,Promotor Regions,Promotor, Genetic,Pseudopromoter, Genetic,Early Promoter, Genetic,Genetic Late Promoter,Genetic Middle Promoters,Genetic Promoter,Genetic Promoter Region,Genetic Promoter Regions,Genetic Promoters,Genetic Promotor,Genetic Promotors,Genetic Pseudopromoter,Genetic Pseudopromoters,Late Promoter, Genetic,Middle Promoter, Genetic,Promoter Region,Promoter Region, Genetic,Promoter, Genetic Early,Promoter, rRNA,Promoters, Genetic,Promoters, Genetic Middle,Promoters, rRNA,Promotor Region,Promotors, Genetic,Pseudopromoters, Genetic,Region, Genetic Promoter,Region, Promoter,Region, Promotor,Regions, Genetic Promoter,Regions, Promoter,Regions, Promotor,rRNA Promoters
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D004926 Escherichia coli A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc. Alkalescens-Dispar Group,Bacillus coli,Bacterium coli,Bacterium coli commune,Diffusely Adherent Escherichia coli,E coli,EAggEC,Enteroaggregative Escherichia coli,Enterococcus coli,Diffusely Adherent E. coli,Enteroaggregative E. coli,Enteroinvasive E. coli,Enteroinvasive Escherichia coli
D000952 Antigens, Polyomavirus Transforming Polyomavirus antigens which cause infection and cellular transformation. The large T antigen is necessary for the initiation of viral DNA synthesis, repression of transcription of the early region and is responsible in conjunction with the middle T antigen for the transformation of primary cells. Small T antigen is necessary for the completion of the productive infection cycle. Polyomavirus Large T Antigens,Polyomavirus Middle T Antigens,Polyomavirus Small T Antigens,Polyomavirus T Proteins,Polyomavirus Transforming Antigens,Polyomavirus Tumor Antigens,SV40 T Antigens,SV40 T Proteins,Simian Sarcoma Virus Proteins,Polyomaviruses Large T Proteins,Polyomaviruses Middle T Proteins,Polyomaviruses Small T Proteins,Antigens, Polyomavirus Tumor,Antigens, SV40 T,Proteins, Polyomavirus T,Proteins, SV40 T,T Antigens, SV40,T Proteins, Polyomavirus,T Proteins, SV40,Transforming Antigens, Polyomavirus,Tumor Antigens, Polyomavirus
D001665 Binding Sites The parts of a macromolecule that directly participate in its specific combination with another molecule. Combining Site,Binding Site,Combining Sites,Site, Binding,Site, Combining,Sites, Binding,Sites, Combining
D012270 Ribosomes Multicomponent ribonucleoprotein structures found in the CYTOPLASM of all cells, and in MITOCHONDRIA, and PLASTIDS. They function in PROTEIN BIOSYNTHESIS via GENETIC TRANSLATION. Ribosome

Related Publications

T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
January 1982, Virology,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
December 1990, Seminars in cancer biology,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
January 1981, Advances in cancer research,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
January 1990, Cell,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
December 1979, Cell,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
February 1986, European journal of biochemistry,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
January 1980, Cold Spring Harbor symposia on quantitative biology,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
December 1978, Proceedings of the National Academy of Sciences of the United States of America,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
August 1981, Biochimica et biophysica acta,
T M Roberts, and B Schaffhausen, and T L Benjamin, and I Bikel, and J Lodge, and D Kaplan
August 1990, Oncogene,
Copied contents to your clipboard!