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Engelke, M. F.

Publications and source records attributed to Engelke, M. F..

3 recordsLinked to original sources

Heterotrimeric kinesin-2 autoinhibition mediated by interactions of the CC2 and proximal tail domains with the motor domains is essential for cilium formation and maintenance

Autoinhibition is a fundamental regulatory mechanism for kinesins, including the heterotrimeric kinesin-2 complex (KIF3A/KIF3B/KAP3), which mediates cytoplasmic cargo transport and anterograde intraflagellar transport. In mammals, kinesin-2 is essential for ciliogenesis and ciliary function. Although a structural model of autoinhibited kinesin-2 has been proposed, further validation and functional analysis are needed. Here, we elucidate the mechanism and functional importance of kinesin-2 autoinhibition using cell-based assays guided by structural predictions. Through knockout-rescue experiments with chimeric KIF3A-KIF3B subunits, we show that subunit-specific interactions between the motor domains and the C-terminal coiled-coil domains and adjacent tail {beta}-hairpin motifs stabilize the autoinhibited state. Interestingly, these same C-terminal regions required for autoinhibition are required for stable heterodimerization of the motor. We further find that a flexible region within the coiled-coil stalk is required for this autoregulation and may facilitate the underlying conformation transitions. Furthermore, the capacity to autoinhibit directly correlates with the ability of mutant motors to support ciliogenesis, underscoring the significance of autoinhibition for motor function. Collectively, these findings define key subunit-specific interactions underlying kinesin-2 autoinhibition, identify elements that govern conformational transitions, and demonstrate that autoinhibition is essential for kinesin-2 function in ciliogenesis.

cell biology↗

Collaborative role of two distinct cilium-specific cytoskeletal systems in driving Hedgehog-responsive transcription factor trafficking

Calibrated transcriptional outputs in cellular signaling require fine regulation of transcription factor activity. In vertebrate Hedgehog (Hh) signaling, the precise output of the final effectors, the GLI (Glioma-associated-oncogene) transcription factors, depends on the primary cilium. In particular, the formation of the activator form of GLI upon pathway initiation requires its concentration at the distal cilium tip. However, the mechanisms underlying this critical step in Hh signaling are unclear. We developed a real-time imaging assay to visualize GLI2, the primary GLI activator isoform, at single particle resolution within the cilium. We observed that GLI2 is a cargo of Intraflagellar Transport (IFT) machinery and is transported with anterograde bias during a restricted time window following pathway activation. Our findings position IFT as a crucial mediator of transcription factor transport within the cilium for vertebrate Hh signaling, in addition to IFTs well-established role in ciliogenesis. Surprisingly, a conserved Hh pathway regulator, the atypical non-motile kinesin KIF7, is critical for the temporal control of GLI2 transport by IFT and the spatial control of GLI2 localization at the cilium tip. This discovery underscores the collaborative role of a motile and a non-motile cilium-specific cytoskeletal system in determining the transcriptional output during Hh signaling.

cell biology↗

Acute inhibition of heterotrimeric kinesin-2 function reveals mechanisms of intraflagellar transport in mammalian cilia

The trafficking of components within cilia, called intraflagellar transport (IFT), is powered by kinesin-2 and dynein-2 motors. Loss of function in any subunit of the heterotrimeric KIF3A/KIF3B/KAP kinesin-2 motor prevents ciliogenesis in mammalian cells and has hindered an understanding of how kinesin-2 motors function in IFT. We used a chemical-genetic approach to engineer an inhibitable KIF3A/KIF3B (i3A/i3B) kinesin-2 motor that is capable of rescuing WT motor function in Kif3a/Kif3b double-knockout cells. Inhibitor addition blocks ciliogenesis or, if added to ciliated cells, blocks IFT within two minutes, which leads to a complete loss of primary cilia within six hours. The kinesin-2 family members KIF3A/KIF3C and KIF17 cannot rescue ciliogenesis in Kif3a/Kif3b double-knockout cells nor delay the disassembly of full-formed cilia upon i3A/i3B inhibition. These data suggest that KIF3A/KIF3B/KAP is the sole and essential motor for cilia assembly and function in mammalian cells, indicating a species-specific adaptation of kinesin-2 motors for IFT function.

cell biology↗