Making more microtubules by severing: a common theme of noncentrosomal microtubule arrays?
- PMID: 17178905
- PMCID: PMC2064694
- DOI: 10.1083/jcb.200611149
Making more microtubules by severing: a common theme of noncentrosomal microtubule arrays?
Abstract
Two related enzymes, katanin and spastin, use the energy from ATP hydrolysis to sever microtubules. Two new studies (one in this issue; see McNally et al., p. 881) show that microtubule severing by katanin provides a means for increasing microtubule density in meiotic spindles. Interestingly, loss of spastin leads to a sparser microtubule array in axons and synaptic boutons. Together, these studies hint at a wider role for microtubule-severing enzymes in the formation and organization of noncentrosomal microtubule arrays by generating new seeds for microtubule growth.
Figures
Comment on
-
Katanin controls mitotic and meiotic spindle length.J Cell Biol. 2006 Dec 18;175(6):881-91. doi: 10.1083/jcb.200608117. J Cell Biol. 2006. PMID: 17178907 Free PMC article.
References
-
- Errico, A., P. Claudiani, M. D'Addio, and E.I. Rugarli. 2004. Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon. Hum. Mol. Genet. 13:2121–2132. - PubMed
-
- Hazan, J., N. Fonknechten, D. Mavel, C. Paternotte, D. Samson, F. Artiguenave, C.S. Davoine, C. Cruaud, A. Durr, P. Wincker, et al. 1999. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat. Genet. 23:296–303. - PubMed
