The Roles of Arl13b in Cilia, Cell Signaling, and Embryonic Development Público
Larkins, Christine Elizabeth (2011)
Abstract
Abstract
The Roles of Arl13b in Cilia, Cell Signaling, and Embryonic
Development
By Christine E Larkins
Cilia are antennae-like projections that are found on the apical
surface of most
vertebrate cells. They were discovered almost a century ago, but
their significance in
multiple cellular events is only beginning to be understood. Cilia
were initially
recognized for their roles in creating motility, however, more
recently it was found that
non-motile primary cilia are required for various cell signaling
events such as signaling
pathway integrity, mechanosensation, and even light detection in
photoreceptor cells.
Mutations in ciliary proteins can lead to a variety of human
syndromes called
ciliopathies. Left-right axis defects are common symptoms in
ciliopathies because axis
establishment in the embryo requires both motile and primary cilia,
but the functions of
primary cilia in the process are less understood. Other common
symptoms, such as
polydactyly, result from defects in the Sonic Hedgehog (Shh)
signaling pathway. Almost
all components of the Shh signaling pathway localize to the cilium
which is required for
pathway integrity. However, it is not clear how Shh signaling
proteins interact within the
cilium or why cilia are required for pathway integrity. Taken
together, a better
understanding of cilia protein function and their roles in
embryonic development and
signaling events is required for grasping the etiology of
ciliopathies.
This dissertation focuses on understanding the function of the
cilia protein
Arl13b, which is mutated in the ciliopathy Joubert Syndrome. Loss
of Arl13b leads to
shortened cilia with a defect in cilia ultrastructure, although the
precise function of
Arl13b in cilia is not clear. Mouse mutants lacking Arl13b,
Arl13bhennin, have both left-
right axis and Shh signaling defects. This dissertation examines
the defects in
establishing the left-right axis in Arl13bhennin mutant
embryos and investigates the
function of Arl13b in ciliogenesis and Shh signaling. Through
examining these processes
I have found that Arl13b is important for maintaining proper levels
of ciliary
components, which is important for both Shh signaling and cilia
structure, and I have
shown that Arl13b may have additional roles outside of the cilium
that are required for
left-right axis establishment.
The Roles of Arl13b in Cilia, Cell Signaling, and Embryonic
Development
By
Christine E Larkins
B.S., College of Charleston, 2005
Advisor: Tamara Caspary
A dissertation submitted to the Faculty of the
James T. Laney School of Graduate Studies of Emory University
in partial fulfillment of the requirements for the degree of
Doctor of Philosophy
in Biochemistry Cell and Developmental Biology
2010
Table of Contents
TABLE OF CONTENTS
Chapter 1: Cilia, Signaling, and Embryonic Development
1
1.1 The Significance of Cilia 2
1.2 Cilia Structure, Building Cilia, and Intraflagellar Transport
3
1.3 Targeting, Transport, and Entry to the Cilium
6
1.4 Cilia in Left-Right Axis Specification
11
1.5 Shh Signaling and Cilia
15
1.6 Arl13b Function in Cilia and Shh Signaling
19
Chapter 2: Materials and Methods
28
Chapter 3: The Cilia Protein Arl13b is Required for Efficient
Nodal Signaling
Activity During Left-Right Axis Specification in Mouse
39
3.1 Summary
40
3.2 Introduction
40
3.3 Results
43
3.4 Discussion
49
Chapter 4: Arl13b Regulates Ciliogenesis and the Dynamic
Localization of
Shh Signaling Proteins
65
4.1 Summary
66
4.2 Introduction
66
4.3 Results
68
4.4 Discussion
77
Chapter 5: Models of Arl13b Function
94
5.1 Arl13b in Nodal Signaling
95
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