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. 2018 Feb 28;7:e32692. doi: 10.7554/eLife.32692

Key resources table.

Reagent type (species)
or resource
Designation Source or reference Identifiers Additional information
cell line (Homo
sapiens, Male)
HCT116 cells Other RRID:CVCL_0291 Prescott Deininger at Tulane
Univeristy LCRC
cell line
(H. sapiens, Male)
HCT116 + Mlh1 This paper NA HCT116 cells stably expressing
human Mlh1-ORF via
lentivirus-mediated integration
cell line
(H. sapiens, Male)
Exo-; Exonuclease-deficient
HCT116 Cells
This paper NA HCT116 cells infected with rAAV
containing D275A and
E277A POLE mutations
cell line
(H. sapiens, Male)
Exo-; Exonuclease-deficient
HCT116 Cells + Mlh1
This paper NA HCT116 cells stably expressing
human Mlh1-ORF via lentivirus-
mediated integration and infected
with rAAV containing D275A and
E277A POLE mutations
recombinant
DNA reagent
ExoI-targeting rAAV vector This paper NA Homology arms/SEPT
Cassette/Exo- mutations
recombinant
DNA reagent
pCMV-XL5-Mlh1 Other NA Victoria Belancio at
Tulane Univeristy LCRC
antibody Mlh1 Antibody Pharmingen G168-728;
RRID: AB_395227
Rabbit monoclonal; (1:100) in Milk
(1%) TBST (1X) x 1 hr at RT
chemical compound, drug 6-Thioguanine; 6-TG Sigma-Aldrich A4882 Used at 5 ug/mL final concentration
chemical compound, drug Hypoxanthine-Aminopterin-
Thymidine; HAT
Thermo Fisher Scientific 21060017 Used at 1X final concentration
chemical compound, drug Geneticin; G418 Thermo Fisher Scientific 10131027 Used at 400 ug/mL
final concentration
other Ad-CMV-Cre Vector Biolabs 1045 Adenovirus expressing Cre
recombinase for excision of SEPT
cassette from ExoI-targeted cell lines
software, algorithm BWA-MEM v0.7.8 PMID: 19451168 NA Used to align reads to
human reference
software, algorithm Picard v1.108 Broad Institute;
https://broadinstitute.github.io/picard/.
NA Identify duplicate reads
software, algorithm The Genome Analysis
Toolkit (GATK) v2.8.1
PMCID: PMC2928508 NA locally realign reads to
known indels and recalibrate
base quality scores
software, algorithm MuTect v1.1.4 PMCID: PMC3833702 NA Identiy somatic point mutations
between the tumour
and matched normal
other WES/WGS raw
sequencing data
This paper NCBI GEO
Accession:
PRJNA327240
Raw FASTQ files for WES and
WGS performed in this study