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Updated: Mar 18, 2026

Purification of Viral DNA for the Identification of Associated Viral and Cellular Proteins
Published on: August 31, 2017
Herpesvirus Late Gene Expression: A Viral-Specific Pre-initiation Complex Is Key
Henri Gruffat1, Roberta Marchione1, Evelyne Manet1
1International Center for Infectiology Research, Oncogenic Herpesviruses Team, Université de Lyon, LyonFrance; Inserm, U1111, LyonFrance.; Ecole Normale Supérieure de Lyon, LyonFrance; CNRS, UMR5308, LyonFrance; Université Lyon 1, LyonFrance.
Herpesvirus gene expression involves immediate-early, early, and late stages. Late gene regulation differs between herpesvirus types, with alphaherpesviruses relying on viral factors and beta/gammaherpesviruses utilizing specific TATT-binding proteins.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Herpesviruses regulate gene expression in a temporal cascade: immediate-early (IE), early (E), and late (L) stages.
- This regulation involves viral/cellular factors and promoter structure differences.
- RNA polymerase II (RNAP-II) transcribes herpesvirus genes, with promoter complexity decreasing from IE to L genes.
Purpose of the Study:
- To compare transcriptional regulation mechanisms of late herpesvirus genes.
- To highlight differences between alphaherpesviruses and beta/gammaherpesviruses.
Main Methods:
- Comparative analysis of herpesvirus promoter structures and regulatory elements.
- Review of existing literature on viral transcription factors and cis-regulating sequences.
Main Results:
- IE and early promoters have cis-regulating sequences and a TATA box.
- Late promoters lack upstream cis-acting sequences and often contain a TATT box in beta/gammaherpesviruses.
- Alphaherpesviruses (e.g., HSV-1) rely on viral IE transcription factors (e.g., ICP4) for late gene regulation.
- Beta/gammaherpesviruses (e.g., EBV) utilize specific TATT-binding proteins for late gene regulation.
Conclusions:
- Late gene transcriptional regulation mechanisms vary significantly across herpesvirus subfamilies.
- Distinct viral factors and promoter architectures dictate the temporal control of herpesvirus replication.
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