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Updated: Jun 5, 2026

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
Published on: December 29, 2015
Rab27a is required for human cytomegalovirus assembly
Alberto Fraile-Ramos1, Victoria Cepeda, Edo Elstak
1Department of Molecular and Cell Biology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Madrid, Spain. alberto.fraile@cnb.csic.es
Abstract:
Human cytomegalovirus (HCMV) completes its final envelopment on intracellular membranes before it is released from the cell. The mechanisms underlying these processes are not understood. Here we studied the role of Rab27a, a regulator of lysosome-related organelle transport, in HCMV production. HCMV infection increased Rab27a expression, and recruitment of Rab27a to membranous strutures at the assembly site. Immuno-gold labelling demonstrated association of Rab27a with viral envelopes. CMV production was reduced after knock-down of Rab27a, and in Rab27a-deficient ashen melanocytes. This study shows a requirement for Rab27a in the CMV life cycle and suggests that CMV and LRO biogenesis share common molecular mechanisms.
Insights
Human cytomegalovirus (HCMV) production requires Rab27a, a protein involved in organelle transport. This study reveals Rab27a
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- Human cytomegalovirus (HCMV) envelopment and release mechanisms remain unclear.
- HCMV final envelopment occurs on intracellular membranes before cell egress.
Purpose of the Study:
- To investigate the role of Rab27a, a known regulator of lysosome-related organelle (LRO) transport, in HCMV production.
- To elucidate the molecular mechanisms governing HCMV assembly and release.
Main Methods:
- Studied Rab27a expression and localization during HCMV infection.
- Utilized immuno-gold labeling to assess Rab27a association with viral envelopes.
- Performed knock-down experiments and analyzed HCMV production in Rab27a-deficient cells (ashen melanocytes).
Main Results:
- HCMV infection upregulated Rab27a expression and recruited it to intracellular assembly sites.
- Rab27a was found associated with viral envelopes via immuno-gold labeling.
- Reduced HCMV production was observed following Rab27a knock-down and in Rab27a-deficient cells.
Conclusions:
- Rab27a is essential for the HCMV life cycle, specifically for viral production.
- HCMV appears to utilize molecular machinery common to lysosome-related organelle biogenesis for its envelopment and release.
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