Minor capsid proteins of mouse polyomavirus are inducers of apoptosis when produced individually but are only moderate contributors to cell death during the late phase of viral infection
Copyright policy )Minor capsid proteins of mouse polyomavirus are inducers of apoptosis when produced individually but are only moderate contributors to cell death during the late phase of viral infection
Minor structural proteins of mouse polyomavirus (MPyV) are essential for virus infection. To study their properties and possible contributions to cell death induction, fusion variants of these proteins, created by linking enhanced green fluorescent protein (EGFP) to their C‐ or N‐termini, were prepared and tested in the absence of other MPyV gene products, namely the tumor antigens and the major capsid protein, VP1. The minor proteins linked to EGFP at their C‐terminus (VP2–EGFP, VP3–EGFP) were found to display properties similar to their nonfused, wild‐type versions: they killed mouse 3T3 cells quickly when expressed individually. Carrying nuclear localization signals at their common C‐terminus, the minor capsid proteins were detected in the nucleus. However, a substantial subpopulation of both VP2 and VP3 proteins, as well as of the fusion proteins VP2–EGFP and VP3–EGFP, was detected in the cytoplasm, co‐localizing with intracellular membranes. Truncated VP3 protein, composed of 103 C‐terminal amino acids, exhibited reduced affinity for intracellular membranes and cytotoxicity. Biochemical studies proved each of the minor proteins to be a very potent inducer of apoptosis, which was dependent on caspase activation. Immuno‐electron microscopy showed the minor proteins to be associated with damaged membranes of the endoplasmic reticulum, nuclear envelope and mitochondria as soon as 5 h post‐transfection. Analysis of apoptotic markers and cell death kinetics in cells transfected with the wild‐type MPyV genome and the genome mutated in both VP2 and VP3 translation start codons revealed that the minor proteins contribute moderately to apoptotic processes in the late phase of infection and both are dispensable for cell destruction at the end of the virus replication cycle.Structured digital abstract MINT‐7386399, MINT‐7386463, MINT‐7386515: VP3 (uniprotkb:P03096‐2) and GRP94 (uniprotkb:P08113) colocalize (MI:0403) by fluorescence microscopy (MI:0416) MINT‐7386328, MINT‐7386434, MINT‐7386493: VP2 (uniprotkb:P03096‐1) and GRP94 (uniprotkb:P08113) colocalize (MI:0403) by fluorescence microscopy (MI:0416) MINT‐7386294, MINT‐7386413, MINT‐7386482: VP2 (uniprotkb:P03096‐1) and Lamin‐B (uniprotkb:P14733) colocalize (MI:0403) by fluorescence microscopy (MI:0416) MINT‐7386354, MINT‐7386450, MINT‐7386504: VP3 (uniprotkb:P12908‐2) and Lamin‐B (uniprotkb:P14733) colocalize (MI:0403) by fluorescence microscopy (MI:0416)
- Charles University Czech Republic
Polyomavirus Infections, Time Factors, Apoptosis, Fibroblasts, Cell Line, Mice, Animals, Capsid Proteins, Polyomavirus, Plasmids
Polyomavirus Infections, Time Factors, Apoptosis, Fibroblasts, Cell Line, Mice, Animals, Capsid Proteins, Polyomavirus, Plasmids
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