» Articles » PMID: 18434595

Global Regulation of the Interphase Microtubule System by Abundantly Expressed Op18/stathmin

Overview
Journal Mol Biol Cell
Date 2008 Apr 25
PMID 18434595
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Op18/stathmin (Op18), a conserved microtubule-depolymerizing and tubulin heterodimer-binding protein, is a major interphase regulator of tubulin monomer-polymer partitioning in diverse cell types in which Op18 is abundant. Here, we addressed the question of whether the microtubule regulatory function of Op18 includes regulation of tubulin heterodimer synthesis. We used two human cell model systems, K562 and Jurkat, combined with strategies for regulatable overexpression or depletion of Op18. Although Op18 depletion caused extensive overpolymerization and increased microtubule content in both cell types, we did not detect any alteration in polymer stability. Interestingly, however, we found that Op18 mediates positive regulation of tubulin heterodimer content in Jurkat cells, which was not observed in K562 cells. By analysis of cells treated with microtubule-poisoning drugs, we found that Jurkat cells regulate tubulin mRNA levels by a posttranscriptional mechanism similarly to normal primary cells, whereas this mechanism is nonfunctional in K562 cells. We present evidence that Op18 mediates posttranscriptional regulation of tubulin mRNA in Jurkat cells through the same basic autoregulatory mechanism as microtubule-poisoning drugs. This, combined with potent regulation of tubulin monomer-polymer partitioning, enables Op18 to exert global regulation of the microtubule system.

Citing Articles

Cell type-specific expression of SEPT3-homology subgroup members controls the subunit number of heteromeric septin complexes.

Sellin M, Stenmark S, Gullberg M Mol Biol Cell. 2014; 25(10):1594-607.

PMID: 24648497 PMC: 4019491. DOI: 10.1091/mbc.E13-09-0553.


Stathmin and microtubules regulate mitotic entry in HeLa cells by controlling activation of both Aurora kinase A and Plk1.

Silva V, Cassimeris L Mol Biol Cell. 2013; 24(24):3819-31.

PMID: 24152729 PMC: 3861079. DOI: 10.1091/mbc.E13-02-0108.


The Microtubule Regulatory Protein Stathmin Is Required to Maintain the Integrity of Axonal Microtubules in Drosophila.

Duncan J, Lytle N, Zuniga A, Goldstein L PLoS One. 2013; 8(6):e68324.

PMID: 23840848 PMC: 3694009. DOI: 10.1371/journal.pone.0068324.


Mammalian SEPT9 isoforms direct microtubule-dependent arrangements of septin core heteromers.

Sellin M, Stenmark S, Gullberg M Mol Biol Cell. 2012; 23(21):4242-55.

PMID: 22956766 PMC: 3484102. DOI: 10.1091/mbc.E12-06-0486.


The microtubule cytoskeleton is required for a G2 cell cycle delay in cancer cells lacking stathmin and p53.

Carney B, Caruso Silva V, Cassimeris L Cytoskeleton (Hoboken). 2012; 69(5):278-89.

PMID: 22407961 PMC: 4004097. DOI: 10.1002/cm.21024.


References
1.
Bachurski C, Theodorakis N, Coulson R, Cleveland D . An amino-terminal tetrapeptide specifies cotranslational degradation of beta-tubulin but not alpha-tubulin mRNAs. Mol Cell Biol. 1994; 14(6):4076-86. PMC: 358773. DOI: 10.1128/mcb.14.6.4076-4086.1994. View

2.
Marklund U, Osterman O, Melander H, Bergh A, Gullberg M . The phenotype of a "Cdc2 kinase target site-deficient" mutant of oncoprotein 18 reveals a role of this protein in cell cycle control. J Biol Chem. 1994; 269(48):30626-35. View

3.
Jourdain L, Curmi P, Sobel A, Pantaloni D, Carlier M . Stathmin: a tubulin-sequestering protein which forms a ternary T2S complex with two tubulin molecules. Biochemistry. 1997; 36(36):10817-21. DOI: 10.1021/bi971491b. View

4.
Belmont L, Mitchison T . Identification of a protein that interacts with tubulin dimers and increases the catastrophe rate of microtubules. Cell. 1996; 84(4):623-31. DOI: 10.1016/s0092-8674(00)81037-5. View

5.
Cleveland D . Autoregulated control of tubulin synthesis in animal cells. Curr Opin Cell Biol. 1989; 1(1):10-4. DOI: 10.1016/s0955-0674(89)80030-4. View