Select your localized edition:

Close ×

More Ways to Connect

Discover one of our 28 local entrepreneurial communities »

Be the first to know as we launch in new countries and markets around the globe.

Interested in bringing MIT Technology Review to your local market?

MIT Technology ReviewMIT Technology Review - logo

 

Unsupported browser: Your browser does not meet modern web standards. See how it scores »

{ action.text }

With the help of new high-speed DNA sequencing technology, scientists have uncovered extensive regions in the human genome where chunks of DNA have been deleted, copied, or completely rearranged. Mapping and characterizing these structural variants could be key to understanding human diversity and the origins of many diseases.

Until recently, most researchers believed that differences among individuals were mainly due to changes in single bases, or “DNA letters.” Over the past couple of years, however, several studies have shown that rearrangements of large chunks of DNA (imagine shuffling around entire sentences, pages, or chapters in a book) could play a more important role. “These are pretty big changes,” says Michael Snyder, a molecular biologist at Yale University. “When you flip around 8,000 bases of DNA, that’s likely to have a dramatic impact.”

Already, studies have linked structural variants in the human genome with several different diseases. For instance, extra copies of a particular gene have been associated with a reduced susceptibility to HIV infection, whereas the full or partial deletion of other genes has been linked to certain forms of heart disease.

In collaboration with 454 Life Sciences, based in Branford, CT, which has developed a novel method of rapidly sequencing DNA (see “Sequencing in a Flash”), Snyder and his colleagues analyzed the genomes of two individuals: one of African descent and one of European descent.

The researchers chopped each genome into millions of fragments, each 3,000 bases long, and then tagged the fragments’ ends. They then sequenced the ends and, using specially designed computer algorithms, mapped the millions of end sequences back to a reference genome, derived from the Human Genome Project.

Most of the time, the end sequences for each fragment lined up just right along the reference genome. However, a certain number did not. “They were either too far apart, too close, or flipped relative to the reference genome,” says Snyder. If a pair of end sequences were too far apart, this meant that an extra chunk of DNA was inserted into that region. If two sequences were closer than expected, a piece of DNA was likely deleted.

Reporting in the September 27 edition of Science Express (the online publication of Science magazine), the researchers found close to 1,300 structural variants between the two genomes–many more than other studies have found. “This is a major form of variation in people,” says Snyder. “It’s much more extensive than people realized.”

Almost half of the structural variants were common between the two individuals, suggesting that these changes in the genome are ancient. Seventeen percent of the structural variants directly affected genes. Most of those affecting genes tended to be involved in the immune system and in the way that the body interacts with the environment, as opposed to genes involved in development.

2 comments. Share your thoughts »

Credit: Yale

Tagged: Biomedicine, DNA, genome, disease

Reprints and Permissions | Send feedback to the editor

From the Archives

Close

Introducing MIT Technology Review Insider.

Already a Magazine subscriber?

You're automatically an Insider. It's easy to activate or upgrade your account.

Activate Your Account

Become an Insider

It's the new way to subscribe. Get even more of the tech news, research, and discoveries you crave.

Sign Up

Learn More

Find out why MIT Technology Review Insider is for you and explore your options.

Show Me