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Genome sequencing becomes cost effective

Combining existing technologies in a unique way could revolutionise genetic research by saving time and money. A once-important but rarely used molecular technique is combined with newer methods.

SOMETIMES THE genius of a discovery lies in how its parts are put together. University of Georgia scientists have combined existing technologies in a unique way that could revolutionise genetic research, saving countless time and hundreds of millions of dollars.

The discovery? Bring back a once-important but now rarely used molecular technique and combine it with newer cloning and DNA sequencing methods. "It can reduce the cost of sequencing entire genomes by 50 to 95 per cent," said Andrew Paterson, director of the UGA Plant Genome Mapping Laboratory and a professor of crop and soil sciences, botany and genetics.

That kind of savings could be staggering. Sequencing the sorghum genome, used as an example to develop the new Cot-based Cloning and Sequencing (CBCS) method, would cost about $7.5 million, compared to $20 million with the current `shotgun' approach.

The difference is in the number of clones that need to be sequenced. Sequencing the onion genome would require 119 million clones. CBCS slashes that to 15 million, eliminating the immense time and $354 million in funding required to do the other 104 million. For the sugar pine, CBCS cuts 281 million required clones to 60 million, knocking down costs by $750 million.

The thing that drives up the time and cost to sequence a genome is its vast number of relatively meaningless DNA sequences. "Repetitive sequences complicate all aspects of gene and genome research," Paterson said.

These highly repetitive sequences are, in essence, genetic junk, said Daniel Peterson, research coordinator with the Plant Genome Mapping Lab. There may be thousands, even millions, of copies of a single sequence. One such sequence, for example, is repeated nearly a million times in the human genome, accounting for nearly 10 percent of human DNA.

"Most of these are ancient viruses," Peterson said. "They're `selfish DNA' making up much of the bulk of a genome but adding nothing to its genetic complexity."

The problem is that to sequence an entire genome, scientists have to wade through these endless copies to get to the genes, which virtually always come in only one or a few copies each.

A technique called Cot analysis makes the savings possible. Developed in the 1960s and widely used in the '70s, it was all but abandoned with the advent of molecular cloning methods. In the late '80s and '90s, research based on Cot analysis bottomed out.

One reason it fell into disuse is that even in the rarefied world of molecular biology, it's a highly demanding process. "You have to be very careful in interpreting the data," Peterson said.

Peterson has been an ardent defender of the value of Cot analysis. The method splits the double strands of DNA into single strands, or denatures them, and then allows them under controlled conditions to renature, or recouples into double strands.

Cot analysis breaks down a complex genome into three populations: highly repetitive (HR), moderately repetitive (MR) and single or low-copy (SL) sequences. It is based on the basic principle that the more highly repetitive sequences will renature faster.

The UGA scientists' breakthrough came when Paterson suggested cloning the separate populations. That made it much easier to separate out, and sequence, the low-copy DNA that includes most of the genes and regulatory (`on-off') switches. "It's like shooting fish in a barrel," Peterson said.

The approach allows researchers to focus their time and funds on the single and low-copy sequences, which comprise a small part of the genome but virtually all of its information content. Paterson and his team have published their findings in the journal Genome Research.

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