Multiple Transgenic Models for Degenerative and Regenerative Research in Zebrafish

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$1,381,869.00
Award Year:
2007
Program:
SBIR
Phase:
Phase II
Contract:
2R44HD047089-02
Award Id:
71394
Agency Tracking Number:
HD047089
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
LUMINOMICS, INC., 1508 S GRAND BLVD, ST. LOUIS, MO, 63104
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
170947977
Principal Investigator:
MEERA SAXENA
(314) 495-9781
MEERA@LUMINOMICS.COM
Business Contact:
JEFFREY MUMM
() -
meera@luminomics.com
Research Institution:
n/a
Abstract
DESCRIPTION (provided by applicant): Zebrafish have a remarkable capacity for cellular regeneration and are amenable to mutational genetic screens. Accordingly, a transgenic zebrafish system that facilitates the removal of specific cell types and the dete ction of regenerative replacement cells has been developed. This inducible ablation platform, termed ZAP (zebrafish ablation-reporter protein), is based on the principle of cytotoxic pro-drug conversion and can be targeted to any genetically definable c ell type. Transgenic expression of ZAPs can therefore be used to model any degenerative condition linked to the loss of specific cells or tissues. ZAPs consist of a pro-drug converting enzyme fused to a fluorescent reporter. The pro-drug converting enzyme converts otherwise innocuous substances into cellular toxins, facilitating inducible elimination of ZAP-expressing cells. The fluorescent reporter allows the presence or absence of targeted cell types to be tracked in living fish. Thus, the ZAP platform pr ovides a means to discovering genetic pathways that regulate the regeneration of specific cell types from discrete adult stem cell populations. Proposed is the creation of a set of transgenic zebrafish lines designed to promote maximum flexibility regardi ng where, when, how much, and what color ZAPs are expressed. The Gal4-UAS system is employed as a modular component that separates transgene expression into elements conferring timing and location (Gal4-expressing activator lines) from elements specifyin g amount and type of transgene product produced (UAS:reporter effector lines). By mating different Gal4 and UAS lines, any expression pattern can be conferred to any reporter/effector gene. An enhancer trap approach, based on Tol2-mediated transposition, will be used to create a series of ~500 Gal4-expressing transgenic lines that allow specific cell types to be targeted. A complimentary series of UAS lines will facilitate control over ZAP expression levels and choice of fluorescent reporter color. Collec tively then, these models will promote insight into the development, function, and regeneration of specific cell types. Accordingly, the transgenic lines generated will be characterized in detail and distributed to the larger research community. The short- term goal is to foster elucidation of the molecular mechanisms regulating adult stem cell niches within the regenerative biology research community. The long-term goal of this project is to promote the development of regenerative therapies capable of rever sing the debilitating effects of degenerative conditions that plague humankind.

* information listed above is at the time of submission.

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