Daily Archives: January 5, 2013

Whole-genome Testing and the Possibility of Gene Therapy for Neurological Disorders
(Visit: http://www.uctv.tv Soon everyone can have their genome sequenced. Will this information improve health, or simply clarify our fate? Series: "MIND Institute Lecture Series on Neurodevelopmental Disorders" [Health and Medicine] [Show ID: 24540]

By: UCtelevision

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Whole-genome Testing and the Possibility of Gene Therapy for Neurological Disorders - Video

WashU Browser: visualizing long-range genome interaction data (Updated)
Visualizing long-range genome interaction data with WashU Epigenome Browser Visit the Browser at: epigenomegateway.wustl.edu Narrated by Rebecca Lowdon Recorded using camStudio (camStudio.org)

By: Xin Zhou

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WashU Browser: visualizing long-range genome interaction data (Updated) - Video

Cancer Genome Institute TV Ad - January 2013

By: FoxChaseCancerCenter

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Cancer Genome Institute TV Ad - January 2013 - Video

Jan. 3, 2013 Researchers at MIT, the Broad Institute and Rockefeller University have developed a new technique for precisely altering the genomes of living cells by adding or deleting genes. The researchers say the technology could offer an easy-to-use, less-expensive way to engineer organisms that produce biofuels; to design animal models to study human disease; and to develop new therapies, among other potential applications.

To create their new genome-editing technique, the researchers modified a set of bacterial proteins that normally defend against viral invaders. Using this system, scientists can alter several genome sites simultaneously and can achieve much greater control over where new genes are inserted, says Feng Zhang, an assistant professor of brain and cognitive sciences at MIT and leader of the research team.

"Anything that requires engineering of an organism to put in new genes or to modify what's in the genome will be able to benefit from this," says Zhang, who is a core member of the Broad Institute and MIT's McGovern Institute for Brain Research.

Zhang and his colleagues describe the new technique in the Jan. 3 online edition of Science. Lead authors of the paper are graduate students Le Cong and Ann Ran.

Early efforts

The first genetically altered mice were created in the 1980s by adding small pieces of DNA to mouse embryonic cells. This method is now widely used to create transgenic mice for the study of human disease, but, because it inserts DNA randomly in the genome, researchers can't target the newly delivered genes to replace existing ones.

In recent years, scientists have sought more precise ways to edit the genome. One such method, known as homologous recombination, involves delivering a piece of DNA that includes the gene of interest flanked by sequences that match the genome region where the gene is to be inserted. However, this technique's success rate is very low because the natural recombination process is rare in normal cells.

More recently, biologists discovered that they could improve the efficiency of this process by adding enzymes called nucleases, which can cut DNA. Zinc fingers are commonly used to deliver the nuclease to a specific location, but zinc finger arrays can't target every possible sequence of DNA, limiting their usefulness. Furthermore, assembling the proteins is a labor-intensive and expensive process.

Complexes known as transcription activator-like effector nucleases (TALENs) can also cut the genome in specific locations, but these complexes can also be expensive and difficult to assemble.

Precise targeting

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Editing genome with high precision: New method to insert multiple genes in specific locations, delete defective genes