Table 3.
Strain name | heat shock plasmidsa | arg-1::gfp reporter | heat shock 20 minb | heat shock 2 hrb | ||
---|---|---|---|---|---|---|
recover 2 hr | recover 20 hr | recover 2 hr | recover 20 hr | |||
AK100c | phs::hlh-8 | none | −d | − | −e | − |
AK107 | none | pZJ19 [−436 to −1] | − | − | − | − |
AK105c | phs::hlh-8 | pZJ19 [−436 to −1] | +/− | + | + | +++ |
AK104 |
phs::hlh-8
phs::hlh-2 |
pZJ19 [−436 to −1] | ++ | ++++ | ++ | ++++ |
Integrated plasmids containing cDNA under the control of the hsp16.41 promoter.
Populations of mixed stage animals of each strain were subjected to heat shock treatment at 33°C for 20 min or 2 hrs followed by recovery at 20°C. The GFP expression pattern of the animals was examined under the fluorescent stereomicroscope during recovery.
Strains AK100 and AK105 also contain hlh-8::gfp, which is a transcriptional reporter that does not contain any coding sequence. This gfp construct was linked to the integrated phs::hlh-8 and could not be crossed out of the strain. However, the difference between the response to heat shock in AK100 compared to AK105 is specific to arg-1::gfp since AK100 has essentially no ectopic expression from hlh-8::gfp.
-:no ectopic GFP expression compared to animals without heat shock treatment; +/−: low level of ectopic GFP expression; +: modest level of ectopic GFP expression; each additional + indicates a significant increase in GFP expression.
Sporadic, low level of ectopic hlh-8::gfp expression was observed in embryos but not larvae after heat shock treatment for 2 hrs and recovery for 4 hrs; the GFP expression disappeared after recovery for 8 hrs.