Microtubules are dynamic structures that serve to organize the cytoplasm in interphase cells and to provide the structural framework and possibly the motive force for the spindle in mitotic cells. The broad objectives of this proposal are to understand microtubule dynamics in vivo and in vitro and to determine whether selected mitotic events are dependent upon the dynamic properties. A variety of experimental approaches will be used including immunofluorescence, microsurgery, fluorescent and hapten tagging of proteins, microinjection and fluorescence photobleaching recovery. The principal aims will be to identify the transformations occurring in the microtubule network at the transition between interphase and mitosis; to determine the extent and sites of exchange of tubulin subunits and microtubule associated proteins with the microtubules: to test for the existence and significance of microtubule treadmilling; and through the use of tubulin-colchicine complex, a specific inhibitor of tubulin exchange, to test the dependence of anaphase motion on microtubule disassembly. Novel methods including hapten-mediated immunoelectorn microscopy and fluorescence photobleaching of fluorescently-tagged proteins incorporated into microtubule polymer will be employed. The results should help elucidate the precise nature and cellular significance of microtubule lability. The results should also be of direct relevance for mechanisms regulating division in normal cells. An understanding of normal cell division may assist in the analysis of cancer cells where the mechanisms restricting division are aberrant.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM025062-07
Application #
3272746
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1978-04-01
Project End
1988-11-30
Budget Start
1984-12-01
Budget End
1985-11-30
Support Year
7
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Graduate Schools
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Lee, Ho-Sup; Komarova, Yulia A; Nadezhdina, Elena S et al. (2010) Phosphorylation controls autoinhibition of cytoplasmic linker protein-170. Mol Biol Cell 21:2661-73
Komarova, Yulia; De Groot, Christian O; Grigoriev, Ilya et al. (2009) Mammalian end binding proteins control persistent microtubule growth. J Cell Biol 184:691-706
Komarova, Yulia; Lansbergen, Gideon; Galjart, Niels et al. (2005) EB1 and EB3 control CLIP dissociation from the ends of growing microtubules. Mol Biol Cell 16:5334-45
Kandere-Grzybowska, Kristiana; Campbell, Christopher; Komarova, Yulia et al. (2005) Molecular dynamics imaging in micropatterned living cells. Nat Methods 2:739-41
Lansbergen, Gideon; Komarova, Yulia; Modesti, Mauro et al. (2004) Conformational changes in CLIP-170 regulate its binding to microtubules and dynactin localization. J Cell Biol 166:1003-14
Kojima, Shin-ichiro; Vignjevic, Danijela; Borisy, Gary G (2004) Improved silencing vector co-expressing GFP and small hairpin RNA. Biotechniques 36:74-9
Chen, Xinyu; Kojima, Shin-ichiro; Borisy, Gary G et al. (2003) p120 catenin associates with kinesin and facilitates the transport of cadherin-catenin complexes to intercellular junctions. J Cell Biol 163:547-57
Bertorello, Alejandro M; Komarova, Yulia; Smith, Kristen et al. (2003) Analysis of Na+,K+-ATPase motion and incorporation into the plasma membrane in response to G protein-coupled receptor signals in living cells. Mol Biol Cell 14:1149-57
Komarova, Yulia A; Vorobjev, Ivan A; Borisy, Gary G (2002) Life cycle of MTs: persistent growth in the cell interior, asymmetric transition frequencies and effects of the cell boundary. J Cell Sci 115:3527-39
Komarova, Yulia A; Akhmanova, Anna S; Kojima, Shin-Ichiro et al. (2002) Cytoplasmic linker proteins promote microtubule rescue in vivo. J Cell Biol 159:589-99

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