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Table 1 Knock-in cell models and isogenic control cells. Knock-in cell models were generated with rAVV mediated gene editing. Mutation status for KRAS and BRAF oncogene genes in each of the isogenic knock-ins and control cell lines were validated by Sanger sequencing

From: Common and mutation specific phenotypes of KRAS and BRAF mutations in colorectal cancer cells revealed by integrative -omics analysis

Designations

Clone

BRAF c.1799T> A (V600E)

BRAF genotype

KRAS

KRAS genotype

Reference

c.38G>A (G13D)

c.34G>T (G12C)

c.35G>T (G12V)

c.35G>A (G12D)

HCT116

Parental

T

wt

G/A

G

G

G

wt/G13D

(Brattain et al. 1981 [22])

HCT116 KRAS WT

DK(HD)

T

Wt

G

G

G

G

wt/KO

(Shirasawa et al. 1993) [24]

HCT116 BRAF V600E

MHB3.2

T/A

wt/V600E

G

G

G

G

wt/KO

This work

RKO

Parental

T/A/A

wt/V600E/ V600E

G

G

G

G

wt/wt

(Brattain et al. 1984 [23])

RKO BRAF WT

RB(HD)

T

wt/KO/KO

G

G

G

G

wt/wt

(Yun et al. 2009) [5]

RKO KRAS G13D

MH2.1

T

wt/KO/KO

G/A

G

G

G

wt/G13D

This work

MH3.1

T

G/A

G

G

G

RKO KRAS G12C

MHC1.1

T

wt/KO/KO

G

G/T

G

G

wt/G12C

This work

MHC2.1

T

G

G/T

G

G

RKO KRAS G12V

MHV1.1

T

wt/KO/KO

G

G

G/T

G

wt/G12V

This work

MHV2.2

T

G

G

G/T

G

RKO KRAS G12D

MHD2.1

T

wt/KO/KO

G

G

G

G/A

wt/G12D

This work

MHD1.1

T

G

G

G

G/A