reSeArcH Article
HSPC WT
HSPC MUTMkP WT
MkP MUT
(n = 19)
(n = 16)(n = 17)
(n = 51)
(n = 108)
(n = 240)(n = 25)
(n = 276)
(n = 14)
(n = 23)(n = 14)
(n = 103)
(n = 701)
(n = 149)(n = 229 )
(n = 125 )2345Log(ATF6 module) 24534453434455452345465ET01 ET02 ET03 ET04 ET05P = 4.6 x 10-5P = 1.4 x 10-6P = 0.22P = 0.082P = 0.42P = 1.1 x 10-5P = 0.49P = 0.0021P = 0.0012P = 6.9 x 10-5Log(PERK module) 21231201234123123123123123123401234ET01 ET02 ET03 ET04 ET05P = 0.29P = 0.037P = 0.7P = 0.82P = 0.41P = 0.94P = 0.4P = 0.41P = 0.51P = 0.38345Log(XBP1 module) 234545454545454545456ET01 ET02 ET03 ET04 ET05P = 0.0097P = 8.6 x 10-6P = 0.17P = 0.015P = 0.022P = 0.0022P = 0.1P = 0.0038P = 0.011P = 4.7 x 10-4(n = 862)
(n = 185)(n = 157)
(n = 85)ET01 ET02 ET03 ET04 ET05HSPC WT
HSPC MUTMkP WT
MkP MUTExtended Data Fig. 7 | ATF6 and IRE1 branches of the UPR are
activated in CALR-mutated progenitor cells. By sample (ET01–ET05),
expression of ATF6-, PERK- and XBP1-target genes in the UPR in CALR
wild-type and mutant MkPs and HSPCs (two-sided Wilcoxon rank-sum
test).