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- Title
Coronavirus M Protein Trafficking in Epithelial Cells Utilizes a Myosin Vb Splice Variant and Rab10.
- Authors
Lapierre, Lynne A.; Roland, Joseph T.; Manning, Elizabeth H.; Caldwell, Catherine; Glenn, Honor L.; Vidalain, Pierre-Olivier; Tangy, Frederic; Hogue, Brenda G.; de Haan, C. A. M.; Goldenring, James R.
- Abstract
The membrane (M) glycoprotein of coronaviruses (CoVs) serves as the nidus for virion assembly. Using a yeast two-hybrid screen, we identified the interaction of the cytosolic tail of Murine Hepatitis Virus (MHV-CoV) M protein with Myosin Vb (MYO5B), specifically with the alternative splice variant of cellular MYO5B including exon D (MYO5B+D), which mediates interaction with Rab10. When co-expressed in human lung epithelial A549 and canine kidney epithelial MDCK cells, MYO5B+D co-localized with the MHV-CoV M protein, as well as with the M proteins from Porcine Epidemic Diarrhea Virus (PEDV-CoV), Middle East Respiratory Syndrome (MERS-CoV) and Severe Acute Respiratory Syndrome 2 (SARS-CoV-2). Co-expressed M proteins and MYO5B+D co-localized with endogenous Rab10 and Rab11a. We identified point mutations in MHV-CoV M that blocked the interaction with MYO5B+D in yeast 2-hybrid assays. One of these point mutations (E121K) was previously shown to block MHV-CoV virion assembly and its interaction with MYO5B+D. The E to K mutation at homologous positions in PEDV-CoV, MERS-CoV and SARS-CoV-2 M proteins also blocked colocalization with MYO5B+D. The knockdown of Rab10 blocked the co-localization of M proteins with MYO5B+D and was rescued by re-expression of CFP-Rab10. Our results suggest that CoV M proteins traffic through Rab10-containing systems, in association with MYO5B+D.
- Subjects
SARS-CoV-2; PORCINE epidemic diarrhea virus; MIDDLE East respiratory syndrome; CORONAVIRUSES; LUNGS; EPITHELIAL cells; MYOSIN; ALTERNATIVE RNA splicing
- Publication
Cells (2073-4409), 2024, Vol 13, Issue 2, p126
- ISSN
2073-4409
- Publication type
Article
- DOI
10.3390/cells13020126