Microtubules play essential roles in a variety of cellular processes, including chromosome segregation and organelle transport. They are dynamic polymers that alternate frequently between phases of growing and shrinking, a property that allows the rapid rearrangement of microtubule arrays in response to cellular signals. Microtubule dynamics are regulated, in large part, by a group of proteins referred to as plus-end tracking proteins or +TIPs. Currently, about a dozen conserved +TIP families have been identified in eukaryotes from yeast to human, but the mechanisms by which most of these proteins influence microtubule dynamics are not well understood. In addition to their ability to bind microtubules, most +TIPs interact with several other +TIPs, creating a complex web of +TIP interactions. These interactions are likely to be key regulators of +TIP activities and are the primary focus of this application. We propose to study four +TIPs that play prominent roles in regulating microtubule dynamics in the yeast, S. cerevisiae. These proteins, Bim1, Bik1, Stu1 and Stu2 belong to the +TIP families EB, CLIP, CLASP, and XMAP215, respectively. Our goal is to purify these proteins and determine how they influence microtubule dynamics in an in vitro microtubule assembly system. Then we will combine pairs of proteins to examine how particular +TIP interactions affect their abilities to regulate microtubule dynamics. We have developed all of the necessary assays in preliminary studies with Bim1 and Bik1. We now plan to expand these studies by including Stu1 and Stu2.

Public Health Relevance

Microtubule plus-end-binding proteins (+TIPs) are important regulators of microtubule function in the mitotic spindle where errors can result in aneuploidy and lead to formation of cancers;the +TIPs APC and EB1 are known to be mutated in some human cancers. In addition, +TIPs play key roles in neurons where microtubules are critical for axoplasmic transport;mutations in the +TIPs Lis1 and p150Glued cause diseases affecting brain development and motor neurons. Our studies in yeast allow a combination of biochemical and genetic approaches that is not possible in higher eukaryotes and, given the conserved nature of +TIPs, should contribute to understanding these important processes in human cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM040479-18A2
Application #
7460217
Study Section
Nuclear Dynamics and Transport (NDT)
Program Officer
Deatherage, James F
Project Start
1997-11-01
Project End
2011-08-31
Budget Start
2009-09-30
Budget End
2010-08-31
Support Year
18
Fiscal Year
2009
Total Cost
$187,211
Indirect Cost
Name
Cornell University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
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Blake-Hodek, Kristina A; Cassimeris, Lynne; Huffaker, Tim C (2010) Regulation of microtubule dynamics by Bim1 and Bik1, the budding yeast members of the EB1 and CLIP-170 families of plus-end tracking proteins. Mol Biol Cell 21:2013-23
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