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. 2021 Sep 27;4(12):e202101151. doi: 10.26508/lsa.202101151

Table 1.

Genomic mutations linked to the suppression of abo1∆ cells growth defect.

Suppressor strains Single-nucleotide variant Amino acid modification Protein name Function (protein complex)
abo1∆_supA G>A (3778764) R1303stop Hip3 HIRA complex
abo1∆_supB G>A (3780744) Q643stop
abo1∆_supC A>C (3779930) L914stop
abo1∆_supD T>A (3780930) K581stop
abo1∆_supE A>T (3780247) C808stop
abo1∆_supF ins T (3782449) N74fs
abo1∆_supG G>T (3016457) G307A Slm9
abo1∆_supH C>T (3017455) Q640stop
abo1∆_supI ins A (2539317) I213fs Pcf1 CAF1 complex
abo1∆_supJ T>C (1365405) L83S Hht2 (H3) Histones
abo1∆_supK T>G (4699234) T55P Hhf1 (H4)

Detailed description of the single-nucleotide variants in genes encoding subunits of HIRA and CAF1 histone chaperone complexes or histone H3 and H4 found in the 11 abo1∆_sup (A to K) clones (also see Fig S3). The genomic positions of the single-nucleotide variants are indicated in brackets. >, substitution; ins, insertion; fs, frameshift; stop, non-sense.