The U of T research is published in the Dec. 22 issue of Molecular Cell. The new technique developed by the investigators uses a modified type of "gene chip" and a computer program to accurately monitor alternative splicing, a cellular process through which basic genetic material becomes more complex and acquires the ability to control genetic messages (mRNAs) that are required for the development of complex organisms.
"Now that we can look at mRNA in more detail, it has opened the door to understanding more about some diseases," explains lead investigator Professor Benjamin Blencowe of U of T's Banting and Best Department of Medical Research (BBDMR) and the Department of Medical Genetics and Microbiology, who notes out-of-control RNA splicing is involved in many human diseases, including cancers and birth defects. "The new information we can now obtain could also provide insights into new treatments."
Each cell in the human body contains about 25,000 genes. Although human tissues and organs all have the same genes, some of the genes are "turned on" and others "off". The complete set of genes in humans is only several times that of budding yeast and close to the number found in the significantly less complex nematode worm, C.elegans, a microscopic ringworm.
How very different organisms develop from comparable numbers and types of genes has been a major question since the genetic similarity was discovered. Scientists are trying to understand what turns a gene "off" or "on", or alters its activity when "on" in other words, the process of gene regulation.
The answer may lie in the coding segments (exons) of human genes, which are separated by long, non-coding segments (introns). The exo
Contact: Christina Marshall
University of Toronto