Project 452219

The Doublecortin Family in Development and Disease

452219

The Doublecortin Family in Development and Disease

$960,075
Project Information
Study Type: Unclear
Research Theme: Biomedical
Institution & Funding
Principal Investigator(s): Brouhard, Gary J
Institution: McGill University
CIHR Institute: Genetics
Program: Project Grant
Peer Review Committee: Cell Biology - Molecular/Fundamental
Competition Year: 2021
Term: 5 yrs 0 mth
Abstract Summary

The outermost layer of the brain, just below the skull, is the cerebral cortex. The cerebral cortex is the seat of our intellect, and in healthy people it has many deep folds. In unfortunate cases, however, a genetic mutation causes a loss of these folds, a disease known as "smooth brain," or lissencephaly. The mutations occur in a protein called doublecortin (DCX). DCX works inside of brain cells, or neurons, to control where neurons are located in the brain and how neurons connect to one another. In humans with DCX mutations, neurons are not located properly in the brain and do not make correct connections, causing mental retardation and epilepsy. We know that DCX works by controlling the shape of the "cytoskeleton," a scaffolding system inside of cells that give them structure, much like the scaffolds used at construction sites. The goal of this grant is to understand precisely how DCX controls the shape of the cytoskeleton and to explain why DCX mutations cause disease.

No special research characteristics identified

This project does not include any of the advanced research characteristics tracked in our database.

Keywords
Doublecortin Microtubule