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Fig. 3 | Genome Medicine

Fig. 3

From: Non-canonical antigens are the largest fraction of peptides presented by MHC class I in mismatch repair deficient murine colorectal cancer

Fig. 3

Identification of targeted MAPs in Mlh1+/+ and Mlh1-/- tumor cells. A The peptide list generated from RNAseq analysis of CT26 Mlh1+/+ cells grown in vitro was compared to the corresponding lists obtained after tumor growth in mice (see Table 2). Thus, peptides lost after injection in CT26 Mlh1+/+ post BALB/c M3 mouse and retrieved after inoculation in CT26 Mlh1+/+ post NOD-SCID M2 mouse were selected. The overlap of these two peptide datasets generated the database of CT26 Mlh1+/+ targeted peptides. B Peptide lists generated from RNAseq analysis in Mlh1-/- samples before and after in vivo growth were compared (see Table 2). This allowed the identification of peptides lost after injection in CT26 Mlh1-/- post BALB/c M2, M6, and M7 mice but maintained in CT26 Mlh1-/- post NOD-SCID M5 mouse. The overlap of these two datasets generated a list of peptides from which specific CT26 Mlh1+/+ sequences were removed. The latter list created the targeted peptides database specific to CT26 Mlh1-/-

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