Large scale chemical mutagenesis screens in zebrafish have led to the isolation of mutations affecting about half the estimated 2,400 genes essential for the development of the fish embryo. The embryonic lethal genes of zebrafish are require for the normal patterning, growth and differentiation of the fish embryo, including its internal organ systems. Some of the genes are required for simple embryonic behaviors. Despite the importance of the chemically induced fish mutants for understanding vertebrate development, a limitation of chemical screens is that at present of the chemical screens is that at present it is not possible to clone the mutated genes. This will require the costly development of a zebrafish genome project, followed by positional or candidate-gene cloning approaches. In Drosophilia, a powerful complement to chemical mutagenesis screens has been the use of P-element insertional mutagenesis for rapid cloning of mutant genes. As a complement to chemical mutagenesis in the zebrafish, we have developed a method of insertional mutagenesis for fish using a retroviral vector as the mutagen. In a pilot screen we isolated 5 embryonic lethal mutations and one adult phenotype and have rapidly cloned 3 of the 6 mutated genes. Although less efficient than chemical mutagenesis, the relative ease of cloning mutated genes makes insertional mutagenesis in zebrafish a powerful new technique for performing classical genetics in a vertebrate animals. Here we propose to perform a large scale insertional mutagenesis screen in the fish to isolate mutants defective in embryonic and simple behaviors. We estimate that during the proposed grant period we can isolate approximately 450 insertional mutants, roughly 15-20% of the embryonic lethals of this organism, and can clone many of the mutated genes. Like the 3 genes we have cloned to date, many of these will be noel and all are expected to have human homologues. Some of the genes are expected to have important medical implications, including conceivably the diagnosis and treatment of human diseases.

Agency
National Institute of Health (NIH)
Institute
Fogarty International Center (FIC)
Type
Small Research Grants (R03)
Project #
5R03TW001510-03
Application #
6629370
Study Section
International and Cooperative Projects 1 Study Section (ICP)
Program Officer
Katz, Flora N
Project Start
2001-02-01
Project End
2004-01-31
Budget Start
2003-02-01
Budget End
2004-01-31
Support Year
3
Fiscal Year
2003
Total Cost
$31,800
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Internal Medicine/Medicine
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139