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New technique allows targeted inactivation of genes in research model
Date:5/27/2008

WORCESTER, Mass. Researchers at the University of Massachusetts Medical School (UMMS) report today on a new technique that improves the ability of scientists to target individual genes for inactivationa technique with broad potential implications for both basic science research and human disease. Two scientific teams at UMMS, one led by Scot A. Wolfe, PhD, an assistant professor in the Program in Gene Function & Expression and the Department of Biochemistry & Molecular Pharmacology, and the other by Nathan D. Lawson, PhD, an associate professor in the Program in Gene Function and Expression and the Program in Molecular Medicine, working with a small fishthe zebrafishcommonly used as a model organism in biomedical research, developed a method to create and deliver a tailor-made restriction enzyme that inactivates a specific gene in a zebrafish embryo.

The paper, Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases appears as an Advance Online Publication of the journal Nature Biotechnology (25 May, 2008; http://dx.doi.org/10.1038/nbt1398 ), and was supported by grants from the National Heart, Lung and Blood Institute and the National Institute of General Medical Sciences.

The best way to figure out what a gene does in an organism is to replace it with a non-functional version, breed the individual, and then look at the offspring to see whats wrong with them, said Laurie Tompkins, Ph.D., who oversees genetic mechanisms grants at the National Institute of General Medical Sciences, The problem is that its hard to swap in non-functional genes that are inherited by the offspring. These investigators have devised a way to do this, which will enable many scientists to answer questions that were previously out of reach.

We believe that this work will fundamentally change how researchers make knockoutsresearch organisms in which one or more genes have been genetically engineered to be turned offin many model organisms, said Dr. Wolfe. In this paper, we demonstrate the feasibility of this approach for gene inactivation using the zebrafish, but we believe that this technology should be applicable to other vertebrate and non-vertebrate systems with exciting implications for the development of new models for the study of human disease.

The collaboration between the Lawson and Wolfe laboratories merges the strengths of two different research programs to achieve important advances at the interface of their interests: the Wolfe laboratorys focus on understanding and engineering protein-DNA recognition in zinc finger proteins and the Lawson laboratorys interest in developing new technologies that facilitate biological studies in zebrafish to better understand development and disease.

The zebrafish has really become quite established as a model organism in the past several years, said Dr. Lawson. I began using the zebrafish model to study angiogenesis because of its external development and transparent embryos we can actually watch blood vessels as they grow in the zebrafish embryo. This allows us to gain novel insights into this process that are not easy to make in mouse models. However, we had not previously been able to directly knock out a gene of interest, an approach available in the mouse. The work we have done with the Wolfe lab will open up completely new avenues for our own research and will further strengthen the use of the zebrafish model. More significantly, this technique will now allow us to make zebrafish models that may provide insight into the progression of human vascular disease.


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Contact: Office of Public Affairs
public.affairs@umassmed.edu
508-856-2000
University of Massachusetts Medical School
Source:Eurekalert

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