“Can we create new life out of our digital universe?” asks Craig Venter.
And his answer is, yes, and pretty soon. He walks the TED2008 audience through his latest research into “fourth-generation fuels” — biologically created fuels with CO2 as their feedstock. His talk covers the details of creating brand-new chromosomes using digital technology, the reasons why we would want to do this, and the bioethics of synthetic life.
Peter Dansky talks about the Life Technologies’ Molecular Biology division.
One hour. One kit. Any sample.
Fast track your SNP analysis with the new TaqMan® Sample-to-SNP™ Kit
Human Genome Project; An introduction to the ongoing Human Genome Project. The dynamic 3D animation will take you “inside” for a close up look at the complexity of the cell. Completed in 2003, the Human Genome Project (HGP) was a 13-year project coordinated by the U.S. Department of Energy and the National Institutes of Health. During the early years of the HGP, the Wellcome Trust (U.K.) became a major partner; additional contributions came from Japan, France, Germany, China, and others.
Listen to Dr. Mahendra Rao and Joydeep Goswami, leaders in regenerative medicine for Life Technologies on the future of stem cell research and how the company is helping to advance the science.
Shaf Yousaf, head of the Applied Biosystems SOLiD System, talks about improvements to the genome sequencer.
The Lasker Foundation has announced that Doctors Victor Ambros, Gary Ruvkun, and David Baulcombe won the Lasker Medical Prize for their discovery of micro-RNA molecules, and their role in gene regulation. http://www.sciencentral.com/video/
RNA interference (also called “RNA-mediated interference”, abbreviated RNAi) is a mechanism for RNA-guided regulation of gene expression in which double-stranded ribonucleic acid inhibits the expression of genes with complementary nucleotide sequences. Conserved in most eukaryotic organisms, the RNAi pathway is thought to have evolved as a form of innate immunity against viruses and also plays a major role in regulating development and genome maintenance.
The RNAi pathway is initiated by the enzyme dicer, which cleaves double-stranded RNA (dsRNA) to short double-stranded fragments of 20–25 base pairs. One of the two strands of each fragment, known as the guide strand, is then incorporated into the RNA-induced silencing complex (RISC) and base-pairs with complementary sequences. The most well-studied outcome of this recognition event is a form of post-transcriptional gene silencing. This occurs when the guide strand base pairs with a messenger RNA (mRNA) molecule and induces degradation of the mRNA by argonaute, the catalytic component of the RISC complex. The short RNA fragments are known as small interfering RNA (siRNA) when they derive from exogenous sources and microRNA (miRNA) when they are produced from RNA-coding genes in the cell’s own genome. The RNAi pathway has been particularly well-studied in certain model organisms such as the nematode worm Caenorhabditis elegans, the fruit fly Drosophila melanogaster, and the flowering plant Arabidopsis thaliana.
The selective and robust effect of RNAi on gene expression makes it a valuable research tool, both in cell culture and in living organisms; synthetic dsRNA introduced into cells can induce suppression of specific genes of interest. RNAi may also be used for large-scale screens that systematically shut down each gene in the cell, which can help identify the components necessary for a particular cellular process or an event such as cell division. Exploitation of the pathway is also a promising tool in biotechnology and medicine.
Historically, RNA interference was known by other names, including post transcriptional gene silencing, transgene silencing, and quelling. Only after these apparently-unrelated processes were fully understood did it become clear that they all described the RNAi phenomenon. RNAi has also been confused with antisense suppression of gene expression, which does not act catalytically to degrade mRNA but instead involves single-stranded RNA fragments physically binding to mRNA and blocking translation. In 2006, Andrew Fire and Craig C. Mello shared the Nobel Prize in Physiology or Medicine for their work on RNA interference in the nematode worm C. elegans,[4] which they published in 1998
A video by Genome British Columbia demonstrating gene expression
www.genomicseducation.ca
