The non-mitotic role of HMMR in regulating the localization of TPX2 and the dynamics of microtubules in neurons

Author:

Chen Yi-Ru1ORCID,Tseng Shun-Cheng23ORCID,Hwang Eric1345ORCID

Affiliation:

1. Institute of Molecular Medicine and Bioengineering, National Yang Ming Chiao Tung University

2. Department of Orthopedic Surgery, Changhua Christian Hospital

3. Department of Biological Science and Technology, National Yang Ming Chiao Tung University

4. Institute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University

5. Center for Intelligent Drug Systems and Smart Bio-devices (IDS2B), National Yang Ming Chiao Tung University

Abstract

A functional nervous system is built upon the proper morphogenesis of neurons to establish the intricate connection between them. The microtubule cytoskeleton is known to play various essential roles in this morphogenetic process. While many microtubule-associated proteins (MAPs) have been demonstrated to participate in neuronal morphogenesis, the function of many more remains to be determined. This study focuses on a MAP called HMMR, which was originally identified as a hyaluronan binding protein and later found to possess microtubule and centrosome binding capacity. HMMR exhibits high abundance on neuronal microtubules and altering the level of HMMR significantly affects the morphology of neurons. Instead of confining to the centrosome(s) like cells in mitosis, HMMR localizes to microtubules along axons and dendrites. Furthermore, transiently expressing HMMR enhances the stability of neuronal microtubules and increases the formation frequency of growing microtubules along the neurites. HMMR regulates the microtubule localization of a non-centrosomal microtubule nucleator TPX2 along the neurite, offering an explanation for how HMMR contributes to the promotion of growing microtubules. This study sheds light on how progenitor cells utilize proteins involved in mitosis for non-mitotic functions.

Publisher

eLife Sciences Publications, Ltd

Reference35 articles.

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4. Spatial regulation of Aurora A activity during mitotic spindle assembly requires RHAMM to correctly localize TPX2;Cell Cycle,2014

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