Table 1.
Putative functional SNPs associated with expression (cis-eQTLs with allele frequencies >5%; adjusted p < 0.05).
Transcript differentially expressed | Annotation | SNP | Position SNP | Regulation | Strain Lineage |
Allele frequency** | ||||
---|---|---|---|---|---|---|---|---|---|---|
Gene | Distance (bp) from start codon | Promoter (P)/TSS | Ancient | Modern | ||||||
SNPs in upstream region | Rv0193c | 1 | G226676A | IGR | −105 | — | Up | 1 | 0.973 | 0 |
Rv0326 | — | T392261C | Rv0325 | −12 | — | Up | 1,2 | 0.978 | 0.324 | |
Rv0377 | 6 | T454295C | Rv0376c | −126 | — | Up | 1,2,4.1,4.3.4, 4.8,4.9 | 1 | 0.994 | |
gpdA1 | 4 | T655986G | IGR | −37 | P | Up | 1,2 | 0.976 | 0.324 | |
mce2D | 6 | A690450C | mce2C | −51 | — | Up | 1,2 | 0.976 | 0.324 | |
Rv0669c | 3 | T769663G | IGR | −66 | P | Down | 4.3.3 | 0 | 0.050 | |
Rv0958 | 3 | C1069871T | IGR | −12 | P | Up | 1.1.3 | 0.220 | 0 | |
Rv1096 | 3 | T1224367C | IGR | −18 | P | Down | 1,2,4.1,4.3,4.8 | 1 | 0.976 | |
Rv1503c | 1 | A1694547C | IGR | −3 | — | Up | 1 | 0.973 | 0 | |
fadD31 | 4 | T2177073C | IGR | −14 | TSS/P | Down | 1 | 0.973 | 0 | |
Rv2036 | 3 | C2282058T | Rv2035 | −41 | — | Up | 1.2.2* | 0.157 | 0 | |
Rv2159c | 1 | A2421816G | Rv2160A | −151 | — | Down | 1,2 | 0.977 | 0.323 | |
PE_PGRS38 | 7 | A2424864G | IGR | −18 | TSS | Down | 1 | 0.973 | 0 | |
Rv2712c | 1 | C3025431T | IGR | −103 | P | Up | 1 | 0.971 | 0 | |
vapB22 | 5 | T3137237C | IGR | −13 | P | Up | 1 | 0.973 | 0 | |
yrbE4B | 5 | G3920109T | yrbE4A | −47 | — | Up | 1 | 0.971 | 0 | |
Rv3695 | 2 | T4137190C | IGR | −16 | — | Down | 1 | 0.973 | 0 |
Table showing the candidate transcripts differentially expressed due to SNPs in upstream intergenic regions (IGRs) or within the upstream gene. Annotation of the transcript differentially expressed: 1 – Conserved hypotheticals, 2 – Cell wall and cell processes, 3 – Intermediary metabolism and respiration, 4 – Lipid metabolism, 5 – Virulence, detoxification, adaptation, 6 – Regulatory proteins, 7 – PE/PPE, 8 – information pathways. Distance of the SNP location from the start codon of the transcript is showed as negative when it is upstream and positive when it is located within the gene. TSS = Transcriptional Start Site. *Only one or two samples from the lineage out of the 3 analysed. **Allele frequency refers to the fraction of strains harbouring the SNP in a larger data set (n = 6,218)50; “—“ when not available.