Innovative technique can sequence entire genome from single cell
Mallinckrodt Professor of Chemistry and Chemical Biology Xiaoliang Sunney Xie (from left) has co-authored a paper on gene sequencing with graduate student Alec Chapman and postdoctoral fellow Chenghang Zong. The paper demonstrates a new method for DNA amplification that could signal a breakthrough in genomics.
The notion that police can
identify a suspect based on the tiniest drop of blood or trace of tissue
has long been a staple of TV dramas, but scientists at Harvard have
taken the idea a step further. Using just a single human cell, they can
reproduce an individual’s entire genome.
As described in a Dec. 21 paper in Science, a team of researchers, led by Xiaoliang Sunney Xie,
the Mallinckrodt Professor of Chemistry and Chemical Biology, and made
up of postdoctoral fellow Chenghang Zong, graduate student Alec Chapman,
and former graduate student Sijia Lu, developed a method — dubbed
MALBAC, short for Multiple Annealing and Looping-based Amplification
Cycles — that requires just one cell to reproduce an entire DNA
molecule.
More than three years in the making, the breakthrough technique
offers the potential for early cancer treatment by allowing doctors to
obtain a genetic “fingerprint” of a person’s cancer from circulating
tumor cells. It also could lead to safer prenatal testing for a host of
genetic diseases.
“If you give us a single human cell, we report to you 93 percent of
the genome that contains three billion base pairs, and if there is a
single base mutation, we can identify it with 70 percent detectability,
with no false positives detected,” Xie said. “This is a major
development.”
In a second paper, published simultaneously, researchers from Xie’s
lab worked with scientists at Peking University in China to demonstrate
MALBAC by sequencing 99 sperm cells from one individual and examining
the paternal and maternal contribution to each cell’s genome.
As its name suggests, Xie said, MALBAC is a type of DNA amplification
that allows researchers to duplicate the single DNA molecule present in
a cell many times so it can be analyzed in the lab.
“While other methods of DNA amplification exist, most — like
polymerase chain reaction (PCR) or multiple displacement amplification
(MDA) — suffer from a specific problem,” Xie said. “Because they amplify
exponentially, both have bias. They dramatically amplify some parts of
the genome, but amplify others very little.”
By comparison, he said, MALBAC relies on linear amplification, meaning it is able to minimize the sequence-dependent bias.
Just as it does with other methods, the amplification process begins
by splitting the DNA double helix into two single strands. Xie’s team
then adds a random “primer” — tiny fragments of DNA — that binds in
dozens of locations along each strand.
To extend those primers, Xie’s team used a DNA polymerase, the same
cellular “machine” that synthesizes DNA as cells divide. Using that
machine, researchers are able to extend the primers from as few as seven
bases to as many as 2,000. Upon heating, they break the elongated
primers apart from the original DNA, yielding half products.
When those half products are then amplified using the same primers,
the two ends of the DNA combine, forming a loop that prevents it from
being amplified again. The leftover half products and the original DNA
are subject to another cycle of amplification. After five cycles of such
linear pre-amplification, the full product is amplified by PCR to
produce enough material for sequencing.
Despite the high coverage, DNA polymerases do occasionally make
errors, Xie explained. To ensure that the genome produced by MALBAC is
accurate, researchers turned to a different technique.
“Many diseases are associated with a single base mutation,” Xie said.
“The challenge, however, is that finding one mutation in more than 3
billion base pairs is like looking for a needle in a haystack. Earlier
techniques, like PCR or MDA, start with many cells, making the challenge
even greater; a single mutation simply gets lost in the process.
MALBAC, however, starts with a single cell, so it is easier to identify
those mutations when they happen.”
To ensure MALBAC’s accuracy, Xie’s team simply let the original cell divide.
While the polymerase that researchers use to build the DNA sequence
is highly accurate, only making one mistake per 10,000 bases, letting
the cell divide gives researchers a chance to double check its work.
“The chances of the same mistake being made at the same base position
are about one in 100 million,” Xie said. “If we let the cells divide
again, and sequence three cells, the chances go up to one in 10 billion,
less than the number of bases in the entire DNA molecule, so we can
remove all the false positives.
“Getting that level of accuracy is very important, because if a
doctor tells a patient that he detects a mutation, he doesn’t want to be
wrong,” he continued. “When we use MALBAC, if a mutation appears in two
or three related cells, we know it must be a real mutation.”
As a demonstration of MALBAC’s power, Xie and his team monitored the
mutations that arose in a single cancer cell as it divided over 20
generations, and uncovered as many as 50 newly acquired mutations.
“This is the first time the mutation rate of a human cell has been
measured directly,” Xie said. “Because we can now see the unique, newly
acquired bases, we can study the dynamics of the genome in a way that
was not possible before.”
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