» Articles » PMID: 9585405

Evidence for a Role of CLIP-170 in the Establishment of Metaphase Chromosome Alignment

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1998 Jun 20
PMID 9585405
Citations 56
Authors
Affiliations
Soon will be listed here.
Abstract

CLIPs (cytoplasmic linker proteins) are a class of proteins believed to mediate the initial, static interaction of organelles with microtubules. CLIP-170, the CLIP best characterized to date, is required for in vitro binding of endocytic transport vesicles to microtubules. We report here that CLIP-170 transiently associates with prometaphase chromosome kinetochores and codistributes with dynein and dynactin at kinetochores, but not polar regions, during mitosis. Like dynein and dynactin, a fraction of the total CLIP-170 pool can be detected on kinetochores of unattached chromosomes but not on those that have become aligned at the metaphase plate. The COOH-terminal domain of CLIP-170, when transiently overexpressed, localizes to kinetochores and causes endogenous full-length CLIP-170 to be lost from the kinetochores, resulting in a delay in prometaphase. Overexpression of the dynactin subunit, dynamitin, strongly reduces the amount of CLIP-170 at kinetochores suggesting that CLIP-170 targeting may involve the dynein/dynactin complex. Thus, CLIP-170 may be a linker for cargo in mitosis as well as interphase. However, dynein and dynactin staining at kinetochores are unaffected by this treatment and further overexpression studies indicate that neither CLIP-170 nor dynein and dynactin are required for the formation of kinetochore fibers. Nevertheless, these results strongly suggest that CLIP-170 contributes in some way to kinetochore function in vivo.

Citing Articles

Microtubule organizing centers regulate spindle positioning in mouse oocytes.

Londono-Vasquez D, Rodriguez-Lukey K, Behura S, Balboula A Dev Cell. 2022; 57(2):197-211.e3.

PMID: 35030327 PMC: 8792338. DOI: 10.1016/j.devcel.2021.12.011.


CLASP2 binding to curved microtubule tips promotes flux and stabilizes kinetochore attachments.

Girao H, Okada N, Rodrigues T, Silva A, Figueiredo A, Garcia Z J Cell Biol. 2019; 219(2).

PMID: 31757788 PMC: 7041679. DOI: 10.1083/jcb.201905080.


The kinetochore-microtubule interface at a glance.

Monda J, Cheeseman I J Cell Sci. 2018; 131(16).

PMID: 30115751 PMC: 6127730. DOI: 10.1242/jcs.214577.


Cytoplasmic Linker Protein CLIP170 Negatively Regulates TLR4 Signaling by Targeting the TLR Adaptor Protein TIRAP.

Jakka P, Bhargavi B, Namani S, Murugan S, Splitter G, Radhakrishnan G J Immunol. 2017; 200(2):704-714.

PMID: 29222167 PMC: 5760445. DOI: 10.4049/jimmunol.1601559.


Spindle asymmetry drives non-Mendelian chromosome segregation.

Akera T, Chmatal L, Trimm E, Yang K, Aonbangkhen C, Chenoweth D Science. 2017; 358(6363):668-672.

PMID: 29097549 PMC: 5906099. DOI: 10.1126/science.aan0092.


References
1.
Barton N, Goldstein L . Going mobile: microtubule motors and chromosome segregation. Proc Natl Acad Sci U S A. 1996; 93(5):1735-42. PMC: 39850. DOI: 10.1073/pnas.93.5.1735. View

2.
Hirokawa N . Microtubule organization and dynamics dependent on microtubule-associated proteins. Curr Opin Cell Biol. 1994; 6(1):74-81. DOI: 10.1016/0955-0674(94)90119-8. View

3.
Merdes A, de Mey J . The mechanism of kinetochore-spindle attachment and polewards movement analyzed in PtK2 cells at the prophase-prometaphase transition. Eur J Cell Biol. 1990; 53(2):313-25. View

4.
Gasser S, Laemmli U . Improved methods for the isolation of individual and clustered mitotic chromosomes. Exp Cell Res. 1987; 173(1):85-98. DOI: 10.1016/0014-4827(87)90334-x. View

5.
Goodson H, Valetti C, Kreis T . Motors and membrane traffic. Curr Opin Cell Biol. 1997; 9(1):18-28. DOI: 10.1016/s0955-0674(97)80147-0. View