A model for the expression of CaMV nucleic acid
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Using Reverse Genetics to Manipulate the NSs Gene of the Rift Valley Fever Virus MP-12 Strain to Improve Vaccine Safety and Efficacy
Published on: November 1, 2011
1John Innes Institute, Colney Lane, NR4 7UH, Norwich, U.K..
Abstract:
Analysis of the sequence of CaMV full-length 35S transcript reveals two features which may relate to the translation of open regions I-V. There is a region in the 5' leader sequence which could act as a ribosome binding site. This is followed by a sequence, which is complementary to sequences which are found just upstream to the open regions. The singificance of these sequences is discussed.
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