|
|
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Vol. 13, Issue 2, 698-710, February 2002


§
*Institut National de la Santé et de la Recherche
Médicale U440-Université Pierre et Marie Curie, Institut du
Fer à Moulin, 75005 Paris, France; and §Institut fur
Entwicklungsbiologie, Universität zu Köln, Köln,
D-50931, Germany
Stathmin is a ubiquitous regulatory phosphoprotein, the generic
element of a family of neural phosphoproteins in vertebrates that
possess the capacity to bind tubulin and interfere with microtubule dynamics. Although stathmin and the other proteins of the family have been associated with numerous cell regulations, their biological roles remain elusive, as in particular inactivation of the stathmin gene in the mouse resulted in no clear deleterious phenotype. We
identified stathmin phosphoproteins in
Drosophila, encoded by a unique gene sharing the
intron/exon structure of the vertebrate stathmin and
stathmin family genes. They interfere
with microtubule assembly in vitro, and in vivo when expressed in HeLa
cells. Drosophila stathmin expression is regulated
during embryogenesis: it is high in the migrating germ cells and in the
central and peripheral nervous systems, a pattern resembling that of
mammalian stathmin. Furthermore, RNA interference inactivation of
Drosophila stathmin expression resulted in germ cell
migration arrest at stage 14. It also induced important anomalies in
nervous system development, such as loss of commissures and
longitudinal connectives in the ventral cord, or abnormal chordotonal
neuron organization. In conclusion, a single Drosophila
gene encodes phosphoproteins homologous to the entire vertebrate
stathmin family. We demonstrate for the first time their direct
involvement in major biological processes such as development of the
reproductive and nervous systems.
These authors contributed equally to this work.
Present addresses:
Centre National de la Recherche
Scientifique Unité Mixte Recherche 144, Institut Curie, 75248 Paris Cedex 05, France;
Unité Mixte Recherche
7102 Centre National de la Recherche Scientifique-Université
Pierre et Marie Curie, Neurobiologie des Processus Adaptatifs, 9 quai
Saint Bernard, 75005 Paris, France.
¶
Corresponding author. E-mail address:
sobel{at}ifm.inserm.fr.
This article has been cited by other articles:
![]() |
B. Belletti, M. S. Nicoloso, M. Schiappacassi, S. Berton, F. Lovat, K. Wolf, V. Canzonieri, S. D'Andrea, A. Zucchetto, P. Friedl, et al. Stathmin Activity Influences Sarcoma Cell Shape, Motility, and Metastatic Potential Mol. Biol. Cell, May 1, 2008; 19(5): 2003 - 2013. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Zahedi, M. P. Revelo, S. Barone, Z. Wang, K. Tehrani, D. P. Citron, J. J. Bissler, H. Rabb, and M. Soleimani Stathmin-deficient mice develop fibrosis and show delayed recovery from ischemic-reperfusion injury Am J Physiol Renal Physiol, June 1, 2006; 290(6): F1559 - F1567. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Tararuk, N. Ostman, W. Li, B. Bjorkblom, A. Padzik, J. Zdrojewska, V. Hongisto, T. Herdegen, W. Konopka, M. J. Courtney, et al. JNK1 phosphorylation of SCG10 determines microtubule dynamics and axodendritic length J. Cell Biol., April 24, 2006; 173(2): 265 - 277. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Manna, D. Thrower, H. P. Miller, P. Curmi, and L. Wilson Stathmin Strongly Increases the Minus End Catastrophe Frequency and Induces Rapid Treadmilling of Bovine Brain Microtubules at Steady State in Vitro J. Biol. Chem., January 27, 2006; 281(4): 2071 - 2078. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Giampietro, F. Luzzati, G. Gambarotta, P. Giacobini, E. Boda, A. Fasolo, and I. Perroteau Stathmin Expression Modulates Migratory Properties of GN-11 Neurons in Vitro Endocrinology, April 1, 2005; 146(4): 1825 - 1834. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Southwood, C. He, J. Garbern, J. Kamholz, E. Arroyo, and A. Gow CNS Myelin Paranodes Require Nkx6-2 Homeoprotein Transcriptional Activity for Normal Structure J. Neurosci., December 15, 2004; 24(50): 11215 - 11225. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Miyashita, M. Kanemura, T. Yamazaki, M. Abe, and Y. Sato Vascular Endothelial Zinc Finger 1 Is Involved in the Regulation of Angiogenesis: Possible Contribution of Stathmin/OP18 as a Downstream Target Gene Arterioscler. Thromb. Vasc. Biol., May 1, 2004; 24(5): 878 - 884. [Abstract] [Full Text] |
||||
![]() |
K. Zahedi, Z. Wang, S. Barone, K. Tehrani, N. Yokota, S. Petrovic, H. Rabb, and M. Soleimani Identification of stathmin as a novel marker of cell proliferation in the recovery phase of acute ischemic renal failure Am J Physiol Cell Physiol, May 1, 2004; 286(5): C1203 - C1211. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. JIN, X. O. MAO, B. COTTRELL, B. SCHILLING, L. XIE, R. H. ROW, Y. SUN, A. PEEL, J. CHILDS, G. GENDEH, et al. Proteomic and immunochemical characterization of a role for stathmin in adult neurogenesis FASEB J, February 1, 2004; 18(2): 287 - 299. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Honnappa, B. Cutting, W. Jahnke, J. Seelig, and M. O. Steinmetz Thermodynamics of the Op18/Stathmin-Tubulin Interaction J. Biol. Chem., October 3, 2003; 278(40): 38926 - 38934. [Abstract] [Full Text] [PDF] |
||||