Early in the SARS-CoV-2 replication cycle, interactions between various non-structural proteins (nsps) and host cell factors initiate the formation of double-membrane replication organelles derived from the endoplasmic reticulum of the host cell. These include double-membrane besicles (DMVs) and convoluted membranes (CMs). Double-stranded RNA (dsRNA), often thought to be an intermediate in the replication of coronaviruses, segregates into these DMVs where RNA synthesis has been shown to occur. These double-membrane enclosures for the viral dsRNA, are thought to create a protective microenvironment for viral genomic RNA replication and transcription of subgenomic mRNAs (sg mRNAs) of SARS-CoV-2.
Last updated: Feb., 2021
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Gary Kaiser