Cilia are microtubule-based organelles that are involved in multiple cellular processes including signaling and motility. Protein entry into cilia s a tightly regulated process and defects in cilia-localized proteins are felt to be a root cause of many ciliopathies that manifest as cystic kidney disease, retinitis pigmentosa and/or other defects. The entry of proteins into cilia appears to be controlled at the cilia base where a ciliar pore is hypothesized to exist. Our group has proposed that the ciliary pore is highly analogous to the nuclear pore in its molecular composition and regulatory mechanism. In particular, we have demonstrated that proteins known to be involved in nuclear trafficking - the small GTPase Ran, its binding partners the importins, and nucleoporins - are present at the base or within cilia and regulate protein entry into the ciliary compartment. Based on our Preliminary Data, we now propose a model where two distinct mechanisms regulate entry into the ciliary compartment: entry of cytosolic proteins is regulated by nucleoporins of the ciliary pore complex (CPC) and requires kinesin motors and intraflagellar transport (IFT) whereas entry of membrane proteins is regulated by molecules of the transition zone (TZ) and is IFT-independent. We will test this model using inducible inhibition of nucleoporin and kinesin motor function combined with live-cell, single-molecule, and super-resolution microscopy techniques. These studies will lead the field forward in understanding ciliary gating mechanisms and will make important inroads in defining the nature of the cilia pore and its relation to the nuclear pore.

Public Health Relevance

Recent studies have suggested that defective function of a cellular organelle called the cilium leads to human diseases (ciliopathies) with diverse pathological phenotypes across organ systems. The aim of this proposal is to study mechanisms that control the gated entry of components into this organelle. We propose that the machinery that controls protein movement into cilia is similar to that which controls transport into and out of the nuclear compartment.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM116204-04
Application #
9546777
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Gindhart, Joseph G
Project Start
2015-09-15
Project End
2019-08-31
Budget Start
2018-09-01
Budget End
2019-08-31
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Ruba, Andrew; Luo, Wangxi; Yang, Weidong (2018) Application of High-speed Super-resolution SPEED Microscopy in Live Primary Cilium. J Vis Exp :
Li, Yichen; Luo, Wangxi; Yang, Weidong (2018) Nuclear Transport and Accumulation of Smad Proteins Studied by Single-Molecule Microscopy. Biophys J 114:2243-2251
Mudumbi, Krishna C; Yang, Weidong (2017) Determination of Membrane Protein Distribution on the Nuclear Envelope by Single-Point Single-Molecule FRAP. Curr Protoc Cell Biol 76:21.11.1-21.11.13
Chien, Alexander; Shih, Sheng Min; Bower, Raqual et al. (2017) Dynamics of the IFT machinery at the ciliary tip. Elife 6:
Ma, Jiong; Kelich, Joseph M; Junod, Samuel L et al. (2017) Super-resolution mapping of scaffold nucleoporins in the nuclear pore complex. J Cell Sci 130:1299-1306
Takao, Daisuke; Wang, Liang; Boss, Allison et al. (2017) Protein Interaction Analysis Provides a Map of the Spatial and Temporal Organization of the Ciliary Gating Zone. Curr Biol 27:2296-2306.e3
Luo, Wangxi; Ruba, Andrew; Takao, Daisuke et al. (2017) Axonemal Lumen Dominates Cytosolic Protein Diffusion inside the Primary Cilium. Sci Rep 7:15793
Ruba, Andrew; Yang, Weidong (2016) O-GlcNAc-ylation in the Nuclear Pore Complex. Cell Mol Bioeng 9:227-233
Mudumbi, Krishna C; Schirmer, Eric C; Yang, Weidong (2016) Single-point single-molecule FRAP distinguishes inner and outer nuclear membrane protein distribution. Nat Commun 7:12562
Verhey, Kristen J; Yang, Weidong (2016) Permeability barriers for generating a unique ciliary protein and lipid composition. Curr Opin Cell Biol 41:109-16

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