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[Preprint]. 2020 Oct 13:2020.06.01.127589. [Version 2] doi: 10.1101/2020.06.01.127589

Table 2: Summary of proteins supported by RNAi or CRISPR screen experiments identified by SDREM from time-series bulk and single-cell SARS-CoV-2 expression data sets.

For each protein, we RNA-seq experimental evidence (‘Bu’ for bulk, ‘Sc’ for single-cell, and ‘Both’ for bulk and single-cell), whether it is a known interactor of a SARS-CoV-2 protein and a brief description of the experimental impact on coronavirus load. Table enumerates each protein previously reported to affect coronavirus load in RNAi or CRISPR screen experiments for the set of proteins identified by SDREM from SARS-CoV-2 data (p values: 6.32e–4 for bulk data; 2.50e–3 for single-cell data). Proteins also listed in the top 1000 protein pairs identified by SDREM from either bulk or single-cell data sets are shown in boldface (p values: 7.70e–3 for bulk data; 8.28e–3 for single-cell data).

Gene name RNA-seq SARS-CoV-2 interactor? RNAi supported effect
PISD Bu Y decreased IBV-CoV replication
POU3F2 Bu N decreased IBV-CoV replication
RAB7A Bu Y affected MHV-CoV fusion
decreased SARS-CoV-2 load
UBE2I Bu N decreased IBV-CoV replication
VPS39 Bu Y affected MHV-CoV fusion
ACVR1 Sc Y decreased SARS-CoV replication
CAV2 Sc Y decreased IBV-CoV replication
CSNK2A1 Sc N decreased SARS-CoV replication
ACVR1B Both Y decreased SARS-CoV replication
ATM Both Y decreased SARS-CoV-2 load
CAV1 Both Y decreased IBV-CoV replication
DYNC2H1 Both Y decreased MHV expression
EPHA2 Both Y decreased SARS-CoV replication
G3BP2 Both Y decreased SARS-CoV-2 load
MDH1 Both Y decreased IBV replication
RBX1 Both Y decreased IBV-CoV replication
SMAD3 Both N conferred resistance to SARS-CoV-2
SMAD4 Both N conferred resistance to SARS-CoV-2
SMARCA4 Both N conferred resistance to SARS-CoV-2