Replication of the Carnation Italian ringspot virus genomic RNA in plant cells occurs in multivesicular bodies which develop from the mitochondrial outer membrane during infection. ORF1 in the viral genome encodes a 36 kDa protein, while ORF2 codes for the 95 kDa replicase by readthrough of the ORF1 stop codon. We have shown previously that the N-terminal part of ORF1 contains the information leading to vesiculation of mitochondria and that the 36 kDa protein localizes to mitochondria. Using infection, in vivo expression of green fluorescent protein fusions in plant or yeast cells and in vitro mitochondrial integration assays, we demonstrate here that both the 36 kDa protein and the complete replicase are targeted to mitochondria and anchor into the outer membrane with the N-terminus and C-terminus on the cytosolic side. Analysis of deletion mutants indicated that the anchor sequence is likely to correspond approximately to the amino acid 84-196 region containing two transmembrane domains. No evidence for a matrix-targeting presequence was found and the data suggest that membrane insertion of the viral proteins is mediated by an import receptor-independent signal-anchor mechanism relying on the two transmembrane segments and multiple recognition signals present in the N-terminal part of ORF1.
Mitochondrial targeting and membrane anchoring of a viral replicase in plant and yeast cells
Russo M;Rubino L
2002
Abstract
Replication of the Carnation Italian ringspot virus genomic RNA in plant cells occurs in multivesicular bodies which develop from the mitochondrial outer membrane during infection. ORF1 in the viral genome encodes a 36 kDa protein, while ORF2 codes for the 95 kDa replicase by readthrough of the ORF1 stop codon. We have shown previously that the N-terminal part of ORF1 contains the information leading to vesiculation of mitochondria and that the 36 kDa protein localizes to mitochondria. Using infection, in vivo expression of green fluorescent protein fusions in plant or yeast cells and in vitro mitochondrial integration assays, we demonstrate here that both the 36 kDa protein and the complete replicase are targeted to mitochondria and anchor into the outer membrane with the N-terminus and C-terminus on the cytosolic side. Analysis of deletion mutants indicated that the anchor sequence is likely to correspond approximately to the amino acid 84-196 region containing two transmembrane domains. No evidence for a matrix-targeting presequence was found and the data suggest that membrane insertion of the viral proteins is mediated by an import receptor-independent signal-anchor mechanism relying on the two transmembrane segments and multiple recognition signals present in the N-terminal part of ORF1.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
