Alternative splicing (AS) of precursor messenger RNA molecules can generate immense complexity from just a single gene (1). Intriguingly, AS is greatest in complex tissues such as the human brain, which may explain why several diseases, are caused by defects in RNA-binding proteins that control AS (2). Thus, AS is strongly related to biological complexity and the proper function of complex cell types, like neurons. The most extreme example that demonstrates this relationship is the Down syndrome cell adhesion molecule (Dscam) of Drosophila melanogaster. Dscam can be alternatively splicing to conceivably generate over 38,000 different protein isoforms;without this complexity, neurons do not wire properly (3).
The aim of this proposal is to understand the mechanisms by which Dscam AS is controlled in Drosophila neurons. Preliminary results suggest that the expression of particular Dscam isoforms may be highly biased for specific neurons. How this might occur is not known, but presumably, different combinations of RNA-binding proteins are present in different neurons to determine which Dscam isoforms are produced. Several RNA binding proteins (trans-acting regulators) and RNA sequence elements (cis-acting regulators) are known to be important for Dscam AS;however, little is known about how these factors interact to coordinate specific outcomes. This proposal outlines a research strategy to dissect the mechanisms that control Dscam AS.
Aim 1 will focus on dissecting the combinatorial control of Dscam AS in cell culture.
Aim 2 will test the requirement for specific RNA-binding proteins in individual neurons. And lastly, Aim 3 will identify common regulators between different neurons that express the same Dscam isoforms. Determining how Dscam AS is controlled in Drosophila neurons will open a window to understanding how animals generate biological complexity and promote proper neuronal function.

Public Health Relevance

Alternative splicing of precursor mRNA molecules can generate immense complexity from just a single gene (1). Proper control of alternative splicing decision is important for complex processes like neuronal function;when these processes lose control, they can cause neurological disease (2). Here, we propose to understand how the extraordinarily complex alternative splicing of the Down syndrome cell adhesion molecule (Dscam) is controlled to promote proper neuronal wiring.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM105264-02
Application #
8625644
Study Section
Special Emphasis Panel (ZRG1-F08-Q (20))
Program Officer
Reddy, Michael K
Project Start
2013-03-01
Project End
2016-02-29
Budget Start
2014-03-01
Budget End
2015-02-28
Support Year
2
Fiscal Year
2014
Total Cost
$53,282
Indirect Cost
Name
University of Connecticut
Department
Genetics
Type
Schools of Medicine
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030