Subunit of assembly of Escherichia coli RNA polymerase. 1981

A Ishihama

The isolated subunits of Escherichia coli DNA-dependent RNA polymerase are reassembled in a stepwise manner in the following sequence: 2 alpha leads to alpha 2 leads to alpha 2 beta leads to alpha 2 beta beta' (premature core enzyme) leads to E (active core enzyme). When the in vitro reconstitution is performed at low temperature, the subunit assembly is prevented until the assembled but inactive premature core enzyme is formed, which is similar to native core enzyme in many parameters of gross conformation but differs from it in several minor and local conformations. The temperature-dependent activation of premature core enzyme at a salt concentration as low as that in vivo takes place only in the continuous presence of either the sigma subunit or DNA. The sigma subunit is therefore proposed to be a regulatory protein which influences the conformation of core subunit assembly in multiple ways from the initial enzyme maturation to the final initiation of transcription. Evidence has accumulated which indicates that the subunit assembly in vivo proceeds via the same pathway as that identified in vitro, including the identification of all species of the assembly intermediates in cell extracts, the identification of all possible types of assembly-defective mutants among temperature-sensitive alpha-, beta-, and beta'-subunit mutants, the kinetics of the appearance of pulse-labeled subunits in the enzyme structure as expected from the assembly sequence and the integration of labeled subassemblies into the enzyme structure upon chasing. The functional complexity of RNA polymerase coupled with transcriptional control appears to depend on its structural flexibility which fluctuates through the assembly with various transcription factors. This type of transcriptional control is being thoroughly considered by a final conclusion awaits further examinations.

UI MeSH Term Description Entries
D008970 Molecular Weight The sum of the weight of all the atoms in a molecule. Molecular Weights,Weight, Molecular,Weights, Molecular
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D011487 Protein Conformation The characteristic 3-dimensional shape of a protein, including the secondary, supersecondary (motifs), tertiary (domains) and quaternary structure of the peptide chain. PROTEIN STRUCTURE, QUATERNARY describes the conformation assumed by multimeric proteins (aggregates of more than one polypeptide chain). Conformation, Protein,Conformations, Protein,Protein Conformations
D004789 Enzyme Activation Conversion of an inactive form of an enzyme to one possessing metabolic activity. It includes 1, activation by ions (activators); 2, activation by cofactors (coenzymes); and 3, conversion of an enzyme precursor (proenzyme or zymogen) to an active enzyme. Activation, Enzyme,Activations, Enzyme,Enzyme Activations
D004792 Enzyme Precursors Physiologically inactive substances that can be converted to active enzymes. Enzyme Precursor,Proenzyme,Proenzymes,Zymogen,Zymogens,Precursor, Enzyme,Precursors, Enzyme
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
D012321 DNA-Directed RNA Polymerases Enzymes that catalyze DNA template-directed extension of the 3'-end of an RNA strand one nucleotide at a time. They can initiate a chain de novo. In eukaryotes, three forms of the enzyme have been distinguished on the basis of sensitivity to alpha-amanitin, and the type of RNA synthesized. (From Enzyme Nomenclature, 1992). DNA-Dependent RNA Polymerases,RNA Polymerases,Transcriptases,DNA-Directed RNA Polymerase,RNA Polymerase,Transcriptase,DNA Dependent RNA Polymerases,DNA Directed RNA Polymerase,DNA Directed RNA Polymerases,Polymerase, DNA-Directed RNA,Polymerase, RNA,Polymerases, DNA-Dependent RNA,Polymerases, DNA-Directed RNA,Polymerases, RNA,RNA Polymerase, DNA-Directed,RNA Polymerases, DNA-Dependent,RNA Polymerases, DNA-Directed
D014158 Transcription, Genetic The biosynthesis of RNA carried out on a template of DNA. The biosynthesis of DNA from an RNA template is called REVERSE TRANSCRIPTION. Genetic Transcription
D046911 Macromolecular Substances Compounds and molecular complexes that consist of very large numbers of atoms and are generally over 500 kDa in size. In biological systems macromolecular substances usually can be visualized using ELECTRON MICROSCOPY and are distinguished from ORGANELLES by the lack of a membrane structure. Macromolecular Complexes,Macromolecular Compounds,Macromolecular Compounds and Complexes,Complexes, Macromolecular,Compounds, Macromolecular,Substances, Macromolecular

Related Publications

A Ishihama
May 1995, Proceedings of the National Academy of Sciences of the United States of America,
A Ishihama
September 1973, Proceedings of the National Academy of Sciences of the United States of America,
A Ishihama
January 2012, Nanomedicine : nanotechnology, biology, and medicine,
A Ishihama
April 1995, Current opinion in genetics & development,
Copied contents to your clipboard!