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. 2006 Dec 14;26(2):358–370. doi: 10.1038/sj.emboj.7601479

Table 2.

The HDA-4(S198A) mutation constitutively represses str-1gfp expression

Straina,b % expressing str-1gfp at WT levels n P-values
Wild type 100 120  
kin-29(oy38) 0 120 <0.001
hda-4(oy57) 100 109  
Ex[hda-4hda-4] 100 110  
Ex[hda-4hda-4 (S198A)] 18 112 <0.001
       
kin-29(oy38); Ex[hda-4hda-4] 0 102 <0.001
kin-29(oy38); Ex[hda-4hda-4 (S198A)] 0 105 <0.001
hda-4(oy57); Ex[hda-4hda-4] 100 117  
hda-4(oy57); Ex[hda-4hda-4 (S198A)] 17 115 <0.001
       
kin-29(oy38) hda-4(oy57) 100 119  
kin-29(oy38) hda-4(oy57); Ex[hda-4hda-4] 10 108 <0.001
kin-29(oy38) hda-4(oy57); Ex[hda-4hda-4 (S198A)] 11 110 <0.001
Adult animals grown at 20°C were examined. Shown are the percentages of animals expressing str-1gfp in at least one AWB neuron at wild-type levels (× 50 magnification). P-values were determined using a two-sample t-test between proportions. Only significant differences (P<0.001), compared to wild type, are shown.
aAll strains contain stably integrated str-1gfp fusion genes.
bFor strains carrying extrachromosomal arrays, data shown are the averages of two or more independent transgenic lines. All hda-4 genomic sequences are tagged with gfp coding sequences.