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Published on: May 1, 2019
Modulation of mRNA 3'-End Processing and Transcription Termination in Virus-Infected Cells
Aarthi Vijayakumar1, Annsea Park2, Joan A Steitz1
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, United States.
Viruses disrupt eukaryotic mRNA 3´-end processing, affecting gene expression and host antiviral responses. This viral interference leads to altered transcript levels and host shutoff, impacting cellular machinery.
Area of Science:
- Molecular Biology
- Virology
- Gene Expression Regulation
Background:
- Eukaryotic mRNA 3´-end processing involves pre-mRNA cleavage and polyadenylation, crucial for gene expression.
- Disruption of this process affects mature mRNA levels and is implicated in viral infections.
- Viral proteins can interfere with 3´-end processing machinery, leading to altered transcript levels and host shutoff.
Purpose of the Study:
- To investigate the role of viral interference with eukaryotic mRNA 3´-end processing.
- To understand how viruses modulate host gene expression and antiviral responses through 3´-end processing disruption.
- To explore the mechanisms by which viruses utilize read-through transcripts.
Main Methods:
- Analysis of viral protein interactions with host 3´-end processing factors.
- Quantification of mature mRNA levels and read-through transcripts in infected cells.
- Assessment of host shutoff and antiviral response suppression.
Main Results:
- Viral proteins inhibit pre-mRNA cleavage and polyadenylation, causing read-through transcription.
- Disrupted 3´-end processing leads to decreased mature mRNA levels and suppressed antiviral responses.
- Read-through transcripts exhibit decreased polyadenylation, nuclear retention, and reduced translation.
Conclusions:
- Viral modulation of host 3´-end processing is a key mechanism for viral pathogenesis and host immune evasion.
- Viruses exploit read-through transcripts to manipulate host protein production and cellular functions.
- Understanding these viral strategies is crucial for developing antiviral therapies.
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