lin-65 : met-2

"We found that met-2, a homolog of the mammalian H3K9 methyltransferase SETDB1 (Schultz et al., 2002; Bessler et al., 2010), was required for LIN-65 nuclear accumulation during induction of the UPRmt. met-2(ok2307) mutation strongly blocked the nuclear accumulation of lin-65p::lin-65::mCherry in the intestine on cco-1 RNAi treatment (Figure 2A)."

cox-5B : met-2

"We found that met-2, a homolog of the mammalian H3K9 methyltransferase SETDB1 (Schultz et al., 2002; Bessler et al., 2010), was required for LIN-65 nuclear accumulation during induction of the UPRmt. met-2(ok2307) mutation strongly blocked the nuclear accumulation of lin-65p::lin-65::mCherry in the intestine on cco-1 RNAi treatment (Figure 2A)."

dpy-27 : mix-1

"both wild-type and EQ mutant DPY-27::GFP interacted well with MIX-1(SMC-2 homolog). However, DPY-27::GFP co-IPed better with DPY-26 (kleisin subunit of condensin I and DC) compared to DPY-27(EQ)::GFP, suggesting that ATPase mutation affects SMC-kleisin interaction."

dpy-26 : dpy-27

"both wild-type and EQ mutant DPY-27::GFP interacted well with MIX-1(SMC-2 homolog). However, DPY-27::GFP co-IPed better with DPY-26 (kleisin subunit of condensin I and DC) compared to DPY-27(EQ)::GFP, suggesting that ATPase mutation affects SMC-kleisin interaction."