daf-16 : starvation
"A DAF-16::GFP construct (Henderson and Johnson, 2001), grown in axenic medium, shows no nuclear localization (Fig. 3A)... We also looked at the DAF-16::GFP localization under BDR conditions. We found cytosolic localization when the concentration of the bacteria exceeded 6 x 10^9 cells/ml, and nuclear localization when the animals were fed less than 10^9 cells/ml (Fig. 3D)."
Interaction involving hsp-17
"Additionally, our cryo-EM structure of Hsp17 reveals that in the 24-mer complex, 12 N-terminal regions are involved in its chaperone function. These flexible regions are located on the outside of the spherical oligomer, whereas the other 12 N-terminal regions are engaged in stabilizing interactions in its interior. This allows the same region in Hsp17 to perform different functions depending on the topological context"
glr-1 : training
"In GLR-1::GFP worms, fluorescence is localized to clusters along the ventral cord neurites and in the nerve ring (corresponding to anatomical synaptic markers reported in EM studies) (White et al., 1986). Confocal imaging was used to visualize the GLR-1::GFP. We compared the amount of GLR-1::GFP expression in the ventral cord in trained worms and control worms. Worms that received distributed training 24 hr earlier showed no difference in the number of GLR-1::GFP clusters in the ventral cord; however, the overall length of GFP clusters per worm in the trained worms was significantly shorter than in the control worms (Fig. 3a)."