Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Interaction: WBInteraction000542004

expand all nodes | collapse all nodes | view schema

Name Class

WBInteraction000542004Interaction_typeRegulatoryChange_of_expression_level
InteractorInteractor_overlapping_geneWBGene00006794Interactor_typeTrans_regulated
Expr_patternExpr1864
AntibodyWBAntibody00000222
WBGene00006321Interactor_typeTrans_regulator
Variation_interactorWBVar00248713Interactor_typeTrans_regulator
WBVar00248736Interactor_typeTrans_regulator
Interaction_summaryThe protein level of UNC-60B, the muscle-specific isoform, was greatly reduced in the sup-12 mutants. In contrast, the total level of UNC-60A, the nonmuscle isoform, was not significantly altered by mutations in sup-12 or unc-60B. Similar changes were detected at the mRNA levels: the unc-60B mRNA was reduced as compared with wild type, whereas the unc-60A mRNA was not significantly altered. In wild-type background, the unc-60B mRNA was decreased in the sup-12 mutants. In wild type and the unc-60B(e677) single mutant, UNC-60A was not detectable in body wall muscle when worms were stained for UNC-60A. However, in the unc-60B;sup-12 double mutant and the sup-12 single mutant, UNC-60A protein was detected in the diffuse cytoplasm.
Detection_methodAntibody
In_situ
Northern
Western[cgc3529]:unc-60_a and [cgc3529]:unc-60_b
Regulation_levelPost_transcriptional
Regulation_resultNegative_regulateSubcellular_localizationcytoplasma
PaperWBPaper00024604
RemarkUNC-60A is expressed in a variety of nonmuscle cells. Therefore, changes in the level of UNC-60A in a subset of tissues may not be detected by the Northern blot analysis. The sup-12 mutations have opposite effects on the levels of the two splice variants, unc-60A and unc-60B, in muscle cells. The suppression of the Unc-60 phenotype by sup-12 could be explained by the up-regulation of UNC-60A in muscle, which may compensate for the function of UNC-60B.