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Fig. 2 | BMC Genomics

Fig. 2

From: Multiomics study of a heterotardigrade, Echinisicus testudo, suggests the possibility of convergent evolution of abundant heat-soluble proteins in Tardigrada

Fig. 2

Gene loss and duplication in tardigrades. Coral orange and gray boxes represent genes conserved and lost in all 5 species used in this study. Furthermore, yellow boxes and blue boxes indicate genes conserved only in eutardigrades and in heterotardigrades, respectively. The numbers on the left of the boxes show copy numbers of multiple copy genes in E. testudo. AMPK, 5′ adenosine monophosphate-activated protein kinase; Apaf-1, apoptotic protease-activating factor 1; ATM, ataxia-telangiectasia mutated; ATR, ataxia telangiectasia and Rad3-related protein; BCS1, mitochondrial chaperone BCS1; CAHS, cytosolic abundant heat soluble; CASP3/7/8, caspase 3/7/8; CBP, CREB binding protein; CHK1/2, checkpoint kinase 1/2; Dsup, damage suppressor; Fas; tumor necrosis factor receptor superfamily member 6; FADD, Fas-associated death domain; Gadd45, growth arrest and DNA damage-inducible; GST, glutathione S-transferase; Hif1α, Hypoxia-inducible factor 1-alpha; Hif1β, aryl hydrocarbon receptor nuclear translocator; HSP, heat shock protein; LEAM, late embryogenesis abundant protein mitochondrial; MAHS, mitochondrial abundant heat soluble; mTOR, mechanistic target of rapamycin; PHD, plant homeodomain; p300, Histone acetyltransferase; Rheb, GTP-binding protein Rheb; SAHS, secretory abundant heat soluble; SIRT1, sirtuin 1; SOD, superoxide dismutase; TSC1/2, tuberous sclerosis 1/2; VHL, von Hippel-Lindau tumor suppressor

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