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Finding The ZIP-code For Gene Therapy: Scientists Imitate Viruses To Deliver Therapeutic Genes

Date:
September 2, 2009
Source:
Federation of American Societies for Experimental Biology
Summary:
Australian scientists have developed a new gene therapy vector that uses the same machinery that viruses use to transport their cargo into our cells. As a result, therapeutic DNA can be transferred to a cell's nucleus more efficiently than in the past, raising hopes for more effective treatment of genetic disorders and some types of cancers.
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A research report featured on the cover of the September 2009 print issue of The FASEB Journal describes how Australian scientists developed a new gene therapy vector that uses the same machinery that viruses use to transport their cargo into our cells. As a result of this achievement, therapeutic DNA can be transferred to a cell's nucleus far more efficiently than in the past, raising hopes for more effective treatment of genetic disorders and some types of cancers.

"Through the use of proteins that mimic key functions of viruses for the packaging and transport of therapeutic DNA, we hope to improve the efficiency, and above all, the specificity of human gene therapy," said David Jans, from the Nuclear Signaling Laboratory at Monash University in Victoria, Australia and one of the researchers involved in the work. "Following the creation of efficient, specific and safe DNA delivery vectors, the challenges in human gene therapy will be able to move on from questions of delivery to actual clinical application."

In short, a gene therapy vector is used to deliver a therapeutic gene or a portion of DNA into a cell nucleus similar to how a syringe is used to inject medicines. To create the new gene therapy vector, Jans and colleagues used pieces of different genes to create a protein called a "modular DNA carrier," which can be produced by bacteria. This protein carries therapeutic DNA and delivers it to a cell's nucleus, where it reprograms a cell to function properly. In the laboratory, these carrier proteins were combined with therapeutic DNA and attached to cell membrane receptors and the nuclear import machinery of target cells. In turn, the packaged DNA moved into the cell through the cytoplasm and into the nucleus.

"Effective gene therapy is clearly the best way to treat heritable diseases. It's also an approach to other diseases where the environment or infection messes up our genes." said Gerald Weissmann, M.D., Editor-in-Chief of The FASEB Journal. "The Australians have worked out how viruses identify our nuclear ZIP-code, and have delivered therapeutic genes to the same address. This work opens up a new era of pharmaceutical development."


Story Source:

The above post is reprinted from materials provided by Federation of American Societies for Experimental Biology. Note: Materials may be edited for content and length.


Journal Reference:

  1. Dominic J. Glover, Su May Ng, Adam Mechler, Lisandra L. Martin, and David A. Jans. Multifunctional protein nanocarriers for targeted nuclear gene delivery in nondividing cells. The FASEB Journal, 2009; 23 (9): 2996 DOI: 10.1096/fj.09-131425

Cite This Page:

Federation of American Societies for Experimental Biology. "Finding The ZIP-code For Gene Therapy: Scientists Imitate Viruses To Deliver Therapeutic Genes." ScienceDaily. ScienceDaily, 2 September 2009. <www.sciencedaily.com/releases/2009/08/090831130749.htm>.
Federation of American Societies for Experimental Biology. (2009, September 2). Finding The ZIP-code For Gene Therapy: Scientists Imitate Viruses To Deliver Therapeutic Genes. ScienceDaily. Retrieved July 31, 2015 from www.sciencedaily.com/releases/2009/08/090831130749.htm
Federation of American Societies for Experimental Biology. "Finding The ZIP-code For Gene Therapy: Scientists Imitate Viruses To Deliver Therapeutic Genes." ScienceDaily. www.sciencedaily.com/releases/2009/08/090831130749.htm (accessed July 31, 2015).

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