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Updated: Jan 25, 2026

Spatiotemporal Subcellular Manipulation of the Microtubule Cytoskeleton in the Living Preimplantation Mouse Embryo using Photostatins
Published on: November 30, 2021
Alp7-Mto1 and Alp14 synergize to promote interphase microtubule regrowth from the nuclear envelope
Wenyue Liu1,2,3, Fan Zheng1,2,3, Yucai Wang4
1Division of Molecular and Cell Biophysics, Hefei National Science Center for Physical Sciences, University of Science and Technology of China, Hefei, China.
Abstract:
Microtubules grow not only from the centrosome but also from various noncentrosomal microtubule-organizing centers (MTOCs), including the nuclear envelope (NE) and pre-existing microtubules. The evolutionarily conserved proteins Mto1/CDK5RAP2 and Alp14/TOG/XMAP215 have been shown to be involved in promoting microtubule nucleation. However, it has remained elusive as to how the microtubule nucleation promoting factors are specified to various noncentrosomal MTOCs, particularly the NE, and how these proteins coordinate to organize microtubule assembly. Here, we demonstrate that in the fission yeast Schizosaccharomyces pombe, efficient interphase microtubule growth from the NE requires Alp7/TACC, Alp14/TOG/XMAP215, and Mto1/CDK5RAP2. The absence of Alp7, Alp14, or Mto1 compromises microtubule regrowth on the NE in cells undergoing microtubule repolymerization. We further demonstrate that Alp7 and Mto1 interdependently localize to the NE in cells without microtubules and that Alp14 localizes to the NE in an Alp7 and Mto1-dependent manner. Tethering Mto1 to the NE in cells lacking Alp7 partially restores microtubule number and the efficiency of microtubule generation from the NE. Hence, our study delineates that Alp7, Alp14, and Mto1 work in concert to regulate interphase microtubule regrowth on the NE.
Insights
Alp7, Alp14, and Mto1 proteins coordinate microtubule nucleation at the nuclear envelope (NE). This study reveals their interdependent localization and function in promoting microtubule regrowth from noncentrosomal microtubule-organizing centers (MTOCs).
Area of Science:
- Cell Biology
- Cytoskeleton Dynamics
- Molecular Cell Biology
Background:
- Microtubules organize cellular processes and are nucleated from centrosomes and noncentrosomal microtubule-organizing centers (MTOCs), including the nuclear envelope (NE).
- Proteins like Mto1/CDK5RAP2 and Alp14/TOG/XMAP215 are known microtubule nucleation factors, but their recruitment and coordination at noncentrosomal MTOCs remain unclear.
Purpose of the Study:
- To investigate the roles and coordination of Alp7/TACC, Alp14/TOG/XMAP215, and Mto1/CDK5RAP2 in interphase microtubule nucleation at the NE in fission yeast.
- To elucidate the mechanisms governing the localization and function of these proteins at noncentrosomal MTOCs.
Main Methods:
- Utilized fission yeast (Schizosaccharomyces pombe) as a model system.
- Observed microtubule regrowth dynamics following depolymerization.
- Investigated protein localization at the NE using microscopy.
- Performed genetic manipulations to assess protein dependency and functional rescue.
Main Results:
- Efficient microtubule regrowth from the NE requires Alp7, Alp14, and Mto1.
- Alp7 and Mto1 exhibit interdependent localization to the NE.
- Alp14 localization to the NE is dependent on Alp7 and Mto1.
- Tethering Mto1 to the NE partially rescues microtubule organization in Alp7-deficient cells.
Conclusions:
- Alp7, Alp14, and Mto1 function concertedly to regulate interphase microtubule regrowth from the NE.
- This study defines a novel mechanism for coordinating microtubule nucleation at a key noncentrosomal MTOC.
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