Decoding Human Genes the Goal of New Open-Source Encyclopedia

In an article published in the journal PLoS Biology on April 19, 2011, the project--called ENCODE (Encyclopedia Of DNA Elements)--provides an overview of the team's ongoing efforts to interpret the human genome sequence, as well as a guide for using the vast amounts of data and resources produced so far by the project.

Ross Hardison, a professor of biochemistry and molecular biology at Pennsylvania State University (Penn State; University Park, PA, USA) and one of the lead investigators of the ENCODE Project team, explained that the philosophy behind the project is one of scientific openness, transparency, and collaboration across subdisciplines. ENCODE comes on the heels of the now-complete Human Genome Project--a 13-year effort aimed at identifying all the approximately 20,000 to 25,000 genes in human DNA--which also was based on the belief in open-source data-sharing to further scientific discovery and public understanding of science. The ENCODE Project has accomplished this goal by publishing its database online, and by posting tools to facilitate data use (please see Related Links below).

Dr. Hardison noted there are about 3 billion base pairs in the human genome, making the cataloging and interpretation of the information a colossal task. "We have a very lofty goal: To identify the function of every nucleotide of the human genome,” he said. "Not only are we discovering the genes that give information to cells and make proteins, but we also want to know what determines that the proteins are made in the right cells, and at the appropriate time. Finding the DNA elements that govern this regulated expression of genes is a major goal of ENCODE.”

ENCODE's task is to identify the human genome's functional regions, many of which are quite esoteric, according to Dr. Hardison. Dr. Hardison stated that the ENCODE Project supplies data such as where proteins bind to DNA and where parts of DNA are augmented by additional chemical markers. These proteins and chemical additions are keys to determining how different cells within the human body interpret the language of DNA.

In the article, the scientists reveled how the ENCODE data can be immediately useful in interpreting associations between disease and DNA sequences that can vary from individual to individual--single nucleotide polymorphisms (SNPs). For example, scientists know that DNA variants located upstream of a gene called MYC are associated with multiple cancers, but until recently the mechanism behind this association was a mystery. ENCODE data already have been utilized to confirm that the variants can change binding of specific proteins, leading to enhanced expression of the MYC gene, and therefore, to the development of cancer. ENCODE also has made similar studies possible for thousands of other DNA variants that may be associated with susceptibility to a variety of human diseases.

Another of the principal investigators of the project, Dr. Richard Myers, president and director of the HudsonAlpha Institute for Biotechnology (Huntsville, AL, USA), explained that the ENCODE Project is unique because it requires collaboration from multiple people all over the world at the cutting edge of their fields.

Scientists with the ENCODE Project also are applying up to 20 different tests in 108 commonly used cell lines to compile important data. John Stamatoyannopoulos, an assistant professor of genome sciences and medicine at the University of Washington (Seattle, USA) and another lead investigator, reported that the ENCODE Project has been responsible for producing many assays--molecular-biology procedures for measuring the activity of biochemical agents--that now are fundamental to biology. "Widely used computational tools for processing and interpreting large-scale functional genomic data also have been developed by the project,” Prof. Stamatoyannopoulos said. "The depth, quality, and diversity of the ENCODE data are unprecedented.”

Dr. Hardison noted that the portion of the human genome that actually codes for protein is approximately 1.1%. "That's still a lot of data,” he said, "and to complicate matters even more, most mechanisms for gene expression and regulation lie outside what we call the ‘coding' region of DNA.”

Dr. Hardison explained that scientists have a limited number of tools with which to explore the genome, and one that has been used widely is inter-species comparison. "For example, we can compare humans and chimpanzees and glean some fascinating information,” he concluded, "but very few proteins and other DNA products differ in any fundamental way between humans and chimps. The important difference between us and our close cousins lies in gene expression--the basic level at which genes give rise to traits such as eye color, height, and susceptibility to a particular disease. ENCODE is helping to map the very proteins involved in gene regulation and gene expression. Our paper not only explains how to find the data, but it also explains how to apply the data to interpret the human genome.”

The ENCODE Project is funded, primarily, by the National Human Genome Research Institute of the US National Institutes of Health (Bethesda, MD, USA).

Related Links:
ENCODE Database
Pennsylvania State University