Peer review process
Not revised: This Reviewed Preprint includes the authors’ original preprint (without revision), an eLife assessment, and public reviews.
Read more about eLife’s peer review process.Editors
- Reviewing EditorYamini DalalNational Cancer Institute, Bethesda, United States of America
- Senior EditorYamini DalalNational Cancer Institute, Bethesda, United States of America
Reviewer #1 (Public review):
The manuscript by Sayeed et al. uses a comprehensive series of multi-omics approaches to demonstrate that late-stage human cytomegalovirus (HCMV) infection leads to a marked disruption of TEAD1 activity, a concomitant loss of TEAD1-DNA interactions, and extensive chromatin remodeling. The data are thoroughly presented and provide evidence for the role of TEAD1 in the cellular response to HCMV infection. However, a key question remains unresolved: is the observed disruption of TEAD1 activity a direct consequence of HCMV infection, or could it be secondary to the broader innate antiviral response? In this respect, the study would benefit from experiments that assess the effect of TEAD1 overexpression or knockdown/deletion on HCMV replication dynamics. Such functional assays could help delineate whether TEAD1 perturbation directly influences viral replication or is part of a downstream/indirect cellular response, providing deeper mechanistic insights.
Reviewer #2 (Public review):
Summary:
This work uses genomic and biochemical approaches for HCMV infection in human fibroblasts and retinal epithelial cell lines, followed by comparisons and some validations using strategies such as immunoblots. Based on these analyses, they propose several mechanisms that could contribute to the HCMV-induced diseases, including closing of TEAD1-occupying domains and reduced TEAD1 transcript and protein levels, decreased YAP1 and phospho-YAP1 levels, and exclusion of TEAD1 exon 6.
Strengths:
The genomics experiments were done in duplicates and data analyses show good technical reproducibility. Data analyses are performed to show changes at the transcript and chromatin level changes, followed by some Western blot validations.
Weaknesses:
This work, at the current stage, is quite correlative since no functional studies are done to show any causal links. For readers who are outside the field, some clarifications of the system and design need to be stated.