a-photodynamic-approach-to-study-function-intracellular-vesicle

A Photodynamic Approach to Study Function of Intracellular Vesicle Rupture

Intracellular vesicles (IVs) are formed through endocytosis of vesicles into cytoplasm. IV formation is involved in activating various signal pathways ...

Academia Sinica

How γ-tubulin ring complex (γ-TuRC), a master template for microtubule nucleation, is spatially and temporally regulated for the assembly of new microtubule arrays remains unclear. Here, we report that an evolutionarily conserved microprotein, Mozart1 (Mzt1), regulates subcellular targeting and microtubule formation activity of γ-TuRC at different cell cycle stages. Crystal structures of protein complexes demonstrate that Mzt1 promiscuously interacts with the N-terminal domains of multiple γ-tubulin complex protein subunits in γ-TuRC via an intercalative binding mode. Genetic- and microscopy-based analyses show that promiscuous binding of Mzt1 in γ-TuRC controls specific subcellular localization of γ-TuRC to modulate microtubule nucleation and stabilization in fission yeast. Moreover, we find Mzt1-independent targeting of γ-TuRC to be crucial for mitotic spindle assembly, demonstrating the cell-cycle-dependent regulation and function of γ-TuRC. Our findings reveal a microprotein-mediated regulatory mechanism underlying microtubule cytoskeleton formation, whereby Mzt1 binding promiscuity confers localization specificity on the multi-protein complex γ-TuRC.

Hsiu-Jung Wang

Inflammation Core Facility,
Institute of Biomedical Sciences,
Inflammation Core Facility, Institute of Biomedical Sciences

Academia Sinica

A Photodynamic Approach to Study Function of Intracellular Vesicle Rupture

Hsiu-Jung Wang

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Inflammation Core Facility,Institute of Biomedical Sciences,Inflammation Core Facility, Institute of Biomedical Sciences

Academia Sinica

A Photodynamic Approach to Study Function of Intracellular Vesicle Rupture

Inflammation Core Facility,
Institute of Biomedical Sciences,
Inflammation Core Facility, Institute of Biomedical Sciences