Literature DB >> 16126385

Microtubules cut and run.

Peter W Baas1, Arzu Karabay, Liang Qiang.   

Abstract

There is broad agreement that cells reconfigure their microtubules through rapid bouts of assembly and disassembly, as described by the mechanism known as dynamic instability. However, many cell types have complex patterns of microtubule organization that are not entirely explicable by dynamic instability. There is growing evidence that microtubules can be moved into new patterns of organization by forces generated by molecular motor proteins. Studies on several cell types support a model called 'cut and run' in which long microtubules are stationary, but relatively short microtubules are mobile. In this model, cells mobilize their microtubules by severing them into short pieces, using enzymes such as katanin and spastin that break the lattice of the microtubule polymer. After being reorganized, the short microtubules can once again elongate and lose their mobility. Microtubule severing is also crucial for a variation of 'cut and run' in which the severed microtubules are reorganized by means of treadmilling.

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Year:  2005        PMID: 16126385     DOI: 10.1016/j.tcb.2005.08.004

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  51 in total

1.  Mechanical Effects of Dynamic Binding between Tau Proteins on Microtubules during Axonal Injury.

Authors:  Hossein Ahmadzadeh; Douglas H Smith; Vivek B Shenoy
Journal:  Biophys J       Date:  2015-12-01       Impact factor: 4.033

2.  RhoA regulates dendrite branching in hippocampal neurons by decreasing cypin protein levels.

Authors:  Hongxin Chen; Bonnie L Firestein
Journal:  J Neurosci       Date:  2007-08-01       Impact factor: 6.167

3.  Genome-wide transcription map of an archaeal cell cycle.

Authors:  Magnus Lundgren; Rolf Bernander
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-16       Impact factor: 11.205

4.  The microtubule-severing proteins spastin and katanin participate differently in the formation of axonal branches.

Authors:  Wenqian Yu; Liang Qiang; Joanna M Solowska; Arzu Karabay; Sirin Korulu; Peter W Baas
Journal:  Mol Biol Cell       Date:  2008-01-30       Impact factor: 4.138

5.  Anterograde microtubule transport drives microtubule bending in LLC-PK1 epithelial cells.

Authors:  Andrew D Bicek; Erkan Tüzel; Aleksey Demtchouk; Maruti Uppalapati; William O Hancock; Daniel M Kroll; David J Odde
Journal:  Mol Biol Cell       Date:  2009-04-29       Impact factor: 4.138

Review 6.  Microtubule-severing enzymes at the cutting edge.

Authors:  David J Sharp; Jennifer L Ross
Journal:  J Cell Sci       Date:  2012-05-17       Impact factor: 5.285

7.  Severing and end-to-end annealing of neurofilaments in neurons.

Authors:  Atsuko Uchida; Gülsen Çolakoğlu; Lina Wang; Paula C Monsma; Anthony Brown
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-02       Impact factor: 11.205

8.  Modeling anterograde and retrograde transport of short mobile microtubules from the site of axonal branch formation.

Authors:  I A Kuznetsov; A V Kuznetsov
Journal:  J Biol Phys       Date:  2013-11-24       Impact factor: 1.365

Review 9.  Axonal transport defects in neurodegenerative diseases.

Authors:  Gerardo A Morfini; Matthew Burns; Lester I Binder; Nicholas M Kanaan; Nichole LaPointe; Daryl A Bosco; Robert H Brown; Hannah Brown; Ashutosh Tiwari; Lawrence Hayward; Julia Edgar; Klaus-Armin Nave; James Garberrn; Yuka Atagi; Yuyu Song; Gustavo Pigino; Scott T Brady
Journal:  J Neurosci       Date:  2009-10-14       Impact factor: 6.167

10.  Endocytic membrane fusion and buckling-induced microtubule severing mediate cell abscission.

Authors:  John A Schiel; Kristin Park; Mary K Morphew; Evan Reid; Andreas Hoenger; Rytis Prekeris
Journal:  J Cell Sci       Date:  2011-04-12       Impact factor: 5.285

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