Literature DB >> 17389232

Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing.

Susan Roehl White1, Katia J Evans, Jeffrey Lary, James L Cole, Brett Lauring.   

Abstract

Spastin, an AAA ATPase mutated in the neurodegenerative disease hereditary spastic paraplegia, severs microtubules. Many other AAA proteins form ring-shaped hexamers and contain pore loops, which project into the ring's central cavity and act as ratchets that pull on target proteins, leading, in some cases, to conformational changes. We show that Spastin assembles into a hexamer and that loops within the central pore recognize C-terminal amino acids of tubulin. Key pore loop amino acids are required for severing, including one altered by a disease-associated mutation. We also show that Spastin contains a second microtubule binding domain that makes a distinct interaction with microtubules and is required for severing. Given that Spastin engages the MT in two places and that both interactions are required for severing, we propose that severing occurs by forces exerted on the C-terminal tail of tubulin, which results in a conformational change in tubulin, which releases it from the polymer.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17389232      PMCID: PMC2064084          DOI: 10.1083/jcb.200610072

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  44 in total

1.  A method for directly fitting the time derivative of sedimentation velocity data and an alternative algorithm for calculating sedimentation coefficient distribution functions.

Authors:  J S Philo
Journal:  Anal Biochem       Date:  2000-03-15       Impact factor: 3.365

2.  The 4 A X-ray structure of a tubulin:stathmin-like domain complex.

Authors:  B Gigant; P A Curmi; C Martin-Barbey; E Charbaut; S Lachkar; L Lebeau; S Siavoshian; A Sobel; M Knossow
Journal:  Cell       Date:  2000-09-15       Impact factor: 41.582

3.  Improved methods for fitting sedimentation coefficient distributions derived by time-derivative techniques.

Authors:  John S Philo
Journal:  Anal Biochem       Date:  2006-05-11       Impact factor: 3.365

4.  Substrate specific consequences of central pore mutations in the i-AAA protease Yme1 on substrate engagement.

Authors:  Martin Graef; Thomas Langer
Journal:  J Struct Biol       Date:  2006-02-21       Impact factor: 2.867

5.  Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance.

Authors:  Katia Evans; Christian Keller; Karen Pavur; Kristen Glasgow; Bryan Conn; Brett Lauring
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-30       Impact factor: 11.205

6.  Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.

Authors:  J Hazan; N Fonknechten; D Mavel; C Paternotte; D Samson; F Artiguenave; C S Davoine; C Cruaud; A Dürr; P Wincker; P Brottier; L Cattolico; V Barbe; J M Burgunder; J F Prud'homme; A Brice; B Fontaine; B Heilig; J Weissenbach
Journal:  Nat Genet       Date:  1999-11       Impact factor: 38.330

7.  Microtubule disassembly by ATP-dependent oligomerization of the AAA enzyme katanin.

Authors:  J J Hartman; R D Vale
Journal:  Science       Date:  1999-10-22       Impact factor: 47.728

8.  Structural and mechanistic studies of VPS4 proteins.

Authors:  Anna Scott; Hyo-Young Chung; Malgorzata Gonciarz-Swiatek; Gina C Hill; Frank G Whitby; Jason Gaspar; James M Holton; Ramya Viswanathan; Sanaz Ghaffarian; Christopher P Hill; Wesley I Sundquist
Journal:  EMBO J       Date:  2005-09-29       Impact factor: 11.598

9.  Central pore residues mediate the p97/VCP activity required for ERAD.

Authors:  Byron DeLaBarre; John C Christianson; Ron R Kopito; Axel T Brunger
Journal:  Mol Cell       Date:  2006-05-19       Impact factor: 17.970

10.  Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners.

Authors:  Christopher M Sanderson; James W Connell; Thomas L Edwards; Nicholas A Bright; Simon Duley; Amanda Thompson; J Paul Luzio; Evan Reid
Journal:  Hum Mol Genet       Date:  2005-12-08       Impact factor: 6.150

View more
  70 in total

1.  Nuclear movement during myotube formation is microtubule and dynein dependent and is regulated by Cdc42, Par6 and Par3.

Authors:  Bruno Cadot; Vincent Gache; Elena Vasyutina; Sestina Falcone; Carmen Birchmeier; Edgar R Gomes
Journal:  EMBO Rep       Date:  2012-06-26       Impact factor: 8.807

2.  A common substrate recognition mode conserved between katanin p60 and VPS4 governs microtubule severing and membrane skeleton reorganization.

Authors:  Naoko Iwaya; Yohta Kuwahara; Yoshie Fujiwara; Natsuko Goda; Takeshi Tenno; Kohei Akiyama; Shogo Mase; Hidehito Tochio; Takahisa Ikegami; Masahiro Shirakawa; Hidekazu Hiroaki
Journal:  J Biol Chem       Date:  2010-03-25       Impact factor: 5.157

3.  The C terminus of tubulin, a versatile partner for cationic molecules: binding of Tau, polyamines, and calcium.

Authors:  Julien Lefèvre; Konstantin G Chernov; Vandana Joshi; Stéphanie Delga; Flavio Toma; David Pastré; Patrick A Curmi; Philippe Savarin
Journal:  J Biol Chem       Date:  2010-11-09       Impact factor: 5.157

4.  Katanin Severing and Binding Microtubules Are Inhibited by Tubulin Carboxy Tails.

Authors:  Megan E Bailey; Dan L Sackett; Jennifer L Ross
Journal:  Biophys J       Date:  2015-12-15       Impact factor: 4.033

5.  Binding of Substrates to the Central Pore of the Vps4 ATPase Is Autoinhibited by the Microtubule Interacting and Trafficking (MIT) Domain and Activated by MIT Interacting Motifs (MIMs).

Authors:  Han Han; Nicole Monroe; Jörg Votteler; Binita Shakya; Wesley I Sundquist; Christopher P Hill
Journal:  J Biol Chem       Date:  2015-04-01       Impact factor: 5.157

Review 6.  Tubulin modifications and their cellular functions.

Authors:  Jennetta W Hammond; Dawen Cai; Kristen J Verhey
Journal:  Curr Opin Cell Biol       Date:  2008-01-15       Impact factor: 8.382

7.  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

8.  Two distinct modes of ESCRT-III recognition are required for VPS4 functions in lysosomal protein targeting and HIV-1 budding.

Authors:  Collin Kieffer; Jack J Skalicky; Eiji Morita; Ivana De Domenico; Diane M Ward; Jerry Kaplan; Wesley I Sundquist
Journal:  Dev Cell       Date:  2008-07       Impact factor: 12.270

9.  Molecular basis for class V beta-tubulin effects on microtubule assembly and paclitaxel resistance.

Authors:  Rajat Bhattacharya; Fernando Cabral
Journal:  J Biol Chem       Date:  2009-03-12       Impact factor: 5.157

Review 10.  Microtubule-severing enzymes.

Authors:  Antonina Roll-Mecak; Francis J McNally
Journal:  Curr Opin Cell Biol       Date:  2009-12-05       Impact factor: 8.382

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.