Question
The RNA polymerase from bacteriophage T7 differs structurally from prokaryotic and eukaryotic RNAPs and is extremely specific for its own promoter. Why do these properties make T7 RNAP useful in experiments with recombinant DNA?
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For the in vitro transcription reactions, we used viral RNA polymerase from the T7 bacteriophage instead of a RNA polymerase produced by cells. Read about the composition (subunits) of eukaryotic RNA polymerase II which synthesizes most mRNA in eukaryotic cells and the promoter elements required for it to work. Describe how the T7 virus RNA polymerase differs from eukaryotic RNA polymerase II in composition and required promoter elements.
What is the purpose of RNA processing in eukaryotes? Why don't prokaryotes require similar processing?
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