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SLAIN2 Links Microtubule Plus End-tracking Proteins and Controls Microtubule Growth in Interphase

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 2011 Jun 8
PMID 21646404
Citations 76
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Abstract

The ends of growing microtubules (MTs) accumulate a set of diverse factors known as MT plus end-tracking proteins (+TIPs), which control microtubule dynamics and organization. In this paper, we identify SLAIN2 as a key component of +TIP interaction networks. We showed that the C-terminal part of SLAIN2 bound to end-binding proteins (EBs), cytoplasmic linker proteins (CLIPs), and CLIP-associated proteins and characterized in detail the interaction of SLAIN2 with EB1 and CLIP-170. Furthermore, we found that the N-terminal part of SLAIN2 interacted with ch-TOG, the mammalian homologue of the MT polymerase XMAP215. Through its multiple interactions, SLAIN2 enhanced ch-TOG accumulation at MT plus ends and, as a consequence, strongly stimulated processive MT polymerization in interphase cells. Depletion or disruption of the SLAIN2-ch-TOG complex led to disorganization of the radial MT array. During mitosis, SLAIN2 became highly phosphorylated, and its interaction with EBs and ch-TOG was inhibited. Our study provides new insights into the molecular mechanisms underlying cell cycle-specific regulation of MT polymerization and the organization of the MT network.

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References
1.
Komarova Y, Lansbergen G, Galjart N, Grosveld F, Borisy G, Akhmanova A . EB1 and EB3 control CLIP dissociation from the ends of growing microtubules. Mol Biol Cell. 2005; 16(11):5334-45. PMC: 1266430. DOI: 10.1091/mbc.e05-07-0614. View

2.
Rehberg M, Graf R . Dictyostelium EB1 is a genuine centrosomal component required for proper spindle formation. Mol Biol Cell. 2002; 13(7):2301-10. PMC: 117314. DOI: 10.1091/mbc.e02-01-0054. View

3.
Bonfils C, Bec N, Lacroix B, Harricane M, Larroque C . Kinetic analysis of tubulin assembly in the presence of the microtubule-associated protein TOGp. J Biol Chem. 2006; 282(8):5570-81. PMC: 2238798. DOI: 10.1074/jbc.M605641200. View

4.
Brouhard G, Stear J, Noetzel T, Al-Bassam J, Kinoshita K, Harrison S . XMAP215 is a processive microtubule polymerase. Cell. 2008; 132(1):79-88. PMC: 2311386. DOI: 10.1016/j.cell.2007.11.043. View

5.
Cassimeris L, Becker B, Carney B . TOGp regulates microtubule assembly and density during mitosis and contributes to chromosome directional instability. Cell Motil Cytoskeleton. 2009; 66(8):535-45. DOI: 10.1002/cm.20359. View