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Lack of correlation between Sendai virus P/C mRNA structure and its utilization of two AUG start sites from alternate
1Department of Immunology/Microbiology, Rush Medical College, Chicago, Illinois 60612, USA.
Abstract:
The polycistronic P/C mRNA of Sendai virus encodes five proteins (C', P, C, Y1, and Y2) each of which initiates from a distinct start site. Two major proteins, P and C, are expressed in approximately equimolar amounts from two consecutive AUGs in overlapping reading frames. To better understand the mechanism of expression of the C protein from a downstream AUG, site-directed mutants of the P/C mRNA were created and expressed in COS1 cells. The secondary structure of the mRNA was examined to determine whether the mRNA structure played any role in the synthesis of the C protein. Our results ruled out any significant involvement of the 5' UTR, sequence contexts, secondary structure, distance between the start sites, and sequences downstream to the C-AUG. However, they are consistent with the concept that the synthesis of the C protein is primarily dependent on the orientation of its reading frame, i.e., +1 in relation to the upstream P reading frame. The downstream reading frame was translated poorly when it occurred in +2 orientation in relation to the upstream reading frame. Interestingly, all the known functional bicistronic mRNAs with overlapping reading frames from cytoplasmic RNA viruses have their downstream reading frame in +1 orientation relative to the upstream frame. We propose that the evolutionary conservation of the downstream reading frame in +1 orientation in these bicistronic mRNAs is important for its efficient translation.
Insights
Sendai virus P/C mRNA translation depends on reading frame orientation, not mRNA structure. Efficient C protein expression requires a +1 frame, conserved in viral bicistronic mRNAs for optimal translation.
Area of Science:
- Virology
- Molecular Biology
- Gene Expression
Background:
- Sendai virus polycistronic P/C mRNA encodes five proteins from distinct start sites.
- The P and C proteins are expressed from overlapping reading frames initiated by consecutive AUGs.
Purpose of the Study:
- Investigate the mechanism of C protein expression from a downstream AUG.
- Determine the role of mRNA structure in C protein synthesis.
Main Methods:
- Site-directed mutagenesis of P/C mRNA.
- Expression of mutants in COS1 cells.
- Analysis of mRNA secondary structure.
Main Results:
- mRNA secondary structure, 5' UTR, sequence context, start site distance, and downstream sequences did not significantly affect C protein synthesis.
- C protein expression is primarily dependent on its +1 reading frame orientation relative to the upstream P frame.
- A +2 orientation resulted in poor translation of the downstream reading frame.
Conclusions:
- C protein expression from Sendai virus P/C mRNA is regulated by reading frame orientation.
- The conserved +1 orientation of downstream reading frames in viral bicistronic mRNAs is crucial for efficient translation.