Literature DB >> 10518998

Centrosomal and non-centrosomal microtubules.

T J Keating1, G G Borisy.   

Abstract

While microtubule (MT) arrays in cells are often focused at the centrosome, a variety of cell types contain a substantial number of non-centrosomal MTs. Epithelial cells, neurons, and muscle cells all contain arrays of non-centrosomal MTs that are critical for these cells' specialized functions. There are several routes by which non-centrosomal MTs can arise, including release from the centrosome, cytoplasmic assembly, breakage or severing, and stabilization from non-centrosomal sites. Once formed, MTs that are not tethered to the centrosome must be organized, which can be accomplished by means of self-organization or by capture and nucleation of MTs where they are needed. The presence of free MTs requires stabilization of minus ends, either by MT-associated proteins or by an end-capping complex. Although some of the basic elements of free MT formation and organization are beginning to be understood, a great deal of work is still necessary before we have a complete picture of how non-centrosomal MT arrays are assembled in specific cell types.

Mesh:

Year:  1999        PMID: 10518998

Source DB:  PubMed          Journal:  Biol Cell        ISSN: 0248-4900            Impact factor:   4.458


  39 in total

1.  Organellar relationships in the Golgi region of the pancreatic beta cell line, HIT-T15, visualized by high resolution electron tomography.

Authors:  B J Marsh; D N Mastronarde; K F Buttle; K E Howell; J R McIntosh
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-27       Impact factor: 11.205

2.  Centrosome reorientation in wound-edge cells is cell type specific.

Authors:  Anne-Marie C Yvon; Jonathan W Walker; Barbara Danowski; Carey Fagerstrom; Alexey Khodjakov; Patricia Wadsworth
Journal:  Mol Biol Cell       Date:  2002-06       Impact factor: 4.138

3.  Noncore components of the fission yeast gamma-tubulin complex.

Authors:  Andreas Anders; Paula C C Lourenço; Kenneth E Sawin
Journal:  Mol Biol Cell       Date:  2006-10-04       Impact factor: 4.138

4.  The fission yeast transforming acidic coiled coil-related protein Mia1p/Alp7p is required for formation and maintenance of persistent microtubule-organizing centers at the nuclear envelope.

Authors:  Liling Zheng; Cindi Schwartz; Liangmeng Wee; Snezhana Oliferenko
Journal:  Mol Biol Cell       Date:  2006-02-15       Impact factor: 4.138

Review 5.  Intermediate filaments: a role in epithelial polarity.

Authors:  Andrea S Oriolo; Flavia A Wald; Victoria P Ramsauer; Pedro J I Salas
Journal:  Exp Cell Res       Date:  2007-03-12       Impact factor: 3.905

6.  RanBP10 is a cytoplasmic guanine nucleotide exchange factor that modulates noncentrosomal microtubules.

Authors:  Harald Schulze; Marei Dose; Manav Korpal; Imke Meyer; Joseph E Italiano; Ramesh A Shivdasani
Journal:  J Biol Chem       Date:  2008-03-17       Impact factor: 5.157

Review 7.  Centrosome positioning in vertebrate development.

Authors:  Nan Tang; Wallace F Marshall
Journal:  J Cell Sci       Date:  2012-11-01       Impact factor: 5.285

8.  Delocalization of gamma-tubulin due to increased solubility in human breast cancer cell lines.

Authors:  Edward H Cho; Rebecca A Whipple; Michael A Matrone; Eric M Balzer; Stuart S Martin
Journal:  Cancer Biol Ther       Date:  2010-01-28       Impact factor: 4.742

Review 9.  Cytoplasmic microtubule organization in fission yeast.

Authors:  Kenneth E Sawin; P T Tran
Journal:  Yeast       Date:  2006-10-15       Impact factor: 3.239

10.  Signaling function of alpha-catenin in microtubule regulation.

Authors:  Michael Shtutman; Alexander Chausovsky; Masha Prager-Khoutorsky; Natalia Schiefermeier; Shlomit Boguslavsky; Zvi Kam; Elaine Fuchs; Benjamin Geiger; Gary G Borisy; Alexander D Bershadsky
Journal:  Cell Cycle       Date:  2008-05-30       Impact factor: 4.534

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