(A) We examined ASER cilia shape in N2 and in AMsh::DYN-1(K46A) transgenics animals expressing mKate in ASER. Three categories were made according to ASER cilia shape: animals displaying zero (WT), one, or two filopodia-like protrusions still connected to periciliary membrane compartment (PCMC) (C: cilium; P: filopodial-like protrusion). The percentage of each cilium shape category is given for each genotype. Expression of DYN-1(K46A) transgene in AMsh strongly increased the number of animals showing PCMC protrusions. (B) We examined ASH cilia shape in N2 and in AMsh::DYN-1(K46A) transgenic animals expressing mKate in ASH. Two categories were made according to ASH cilia shape: animals displaying, or not, filopodia-like protrusions still connected to PCMC. AMsh::DYN-1(K46A) strongly increased the number of animals showing PCMC protrusions. (C) We examined AWC wing cilia (WC) with their characteristic membranous expansions in N2 and in AMsh::DYN-1(K46A) transgenics animals expressing DsRed in AWC. Three categories were made according to AWC cilia shape: animals displaying two WC (as wild type), animals displaying one WC and branches instead of the second WC, and animals displaying only branches instead of two WC. In addition, filopodia-like protrusions still connected to PCMC were observed in 11 of 14 AWC animals expressing AMsh::DYN-1(K46A). AMsh::DYN-1(K46A) transgene strongly increased the number of animals showing abnormal AWC cilia; however, AWC cilia was always maintained. (D) Nerve receptive ending (NRE) shape of AFD in N2 and in AMsh::DYN-1(K46A) transgenics expressing mKate in AFD. Five categories were established: wild-type phenotype (WT), abnormal AFD PCMC, abnormal PCMC + elongated microvilli (PCMC + Long Mv), reduced number of microvilli (Less Mv#), and full loss of microvilli (Truncated). AMsh::DYN-1(K46A) transgene strongly increased the number of animals showing abnormal AFD cilia; however, AFD NREs are maintained in 90% of the animals. Scale bar: 5 μm.