By Kim Krieger,
UConn researchers have sequenced the RNA of the most
complicated gene known in nature, using a hand-held sequencer no bigger than a
cell phone.
If DNA is the blueprint of life, RNA is the construction
contractor who interprets it, so sequencing RNA tells you what’s really
happening inside a cell.
Genomicists Brenton Graveley from the UConn Institute of
Systems Genomics, postdoctoral fellow Mohan Bolisetty, and graduate student
Gopinath Rajadinakaran teamed up with UK-based Oxford Nanopore Technologies to
show that the company’s MinION nanopore sequencer can sequence genes faster,
better, and at a much lower cost than the standard technology. They published
their findings on Sept. 30 in Genome Biology.
If your genome was a library and each gene was a book, some
genes would be straightforward reads – but some would be more like a “Choose
Your Own Adventure” novel. Researchers often want to know which version of the
gene is actually expressed in the body, but for complicated
choose-your-own-adventure genes, that has been impossible.
Graveley, Bolisetty, and Rajadinakaran solved the puzzle in
two parts. The first was to find a better gene-sequencing technology. In order
to sequence a gene using the old, existing technology, researchers first make
lots of copies of it, using the same chemistry our bodies use. They then chop
up the gene copies into tiny pieces, read each tiny piece, and then, by
comparing all the different pieces, try to figure out how they were originally
put together. The technique hinges on the likelihood that not all the copies
got chopped up into exactly the same pieces. Imagine watching different scenes
from a movie, out of order. If you then watched the same movie, but cut into
scenes at slightly different places, you could compare the two versions and
start to figure out which scenes connect to which.
That technique won’t work for choose-your-own-adventure
genes, because if you copy them the way the body does, using RNA, each copy can
be slightly – or very – different from the next. Such different versions of the
same gene are called isoforms. When the different isoforms get chopped up and
sequenced, it becomes impossible to accurately compare the pieces and figure
out which versions of the gene you started with.
If the gene were a movie, “you wouldn’t be able to tell that
scenes 1 and 2 were present together,” Bolisetty says.
Then last year, the nearly impossible suddenly became
possible. Oxford Nanopore, a company based in the UK
For the second part of the solution, Graveley, Bolisetty,
and Rajadinakaran decided to go big. Instead of sequencing any old
choose-your-own-adventure gene, they chose the most complex one known, Down
Syndrome cell adhesion molecule 1 (Dscam1), which controls the wiring of the
brain in fruit flies. Dscam1 has the potential of making 38,016 possible isoforms,
and every fruit fly has the potential to make every one of them, yet how many
of these versions are actually made remains unknown. Dscam1 looks like this:
X-12-X-48-X-33-X-2-X, where X’s denote sections that are always the same, and
the numbers indicate sections that can vary (the number itself shows how many
different options there are for that section).
To study how many different isoforms of Dscam1 actually
exist in a fly’s brain, the researchers first had to convert Dscam1 RNA into
DNA. If DNA is the book or set of instructions, RNA is the transcriber that
copies the book so that it can be translated into a protein. The DNA includes
the instructions for all 38,016 isoforms of the Dscam1 gene, while each
individual Dscam1 RNA contains the instructions for just one. No one had yet
used a MinION to sequence copies of RNA, and though it was likely it could be
done, demonstrating it and showing how well it worked would be a substantial
advance in the field.
Rajadinakaran took a fruit fly brain, extracted the RNA,
converted it into DNA, isolated the DNA copies of the Dscam1 RNAs, and then ran
them through the MinION’s nanopores. In this one experiment, they not only
found 7,899 of the 38,016 possible isoforms of Dscam1 were expressed but also
that many more, if not all versions are likely to be expressed.
“A lot of people said ‘The MinION will never work,’”
Graveley says, “but we showed it works using the most complicated gene known.”
The study demonstrates that gene sequencing technology can
now be accessed by a much broader range of researchers than was previously
possible, since the MinION is both relatively inexpensive and highly portable
so that it requires almost no lab space.
“This type of cutting-edge work puts UConn at the forefront
of technology development and strengthens our portfolio of genomics research,”
says Marc Lalande, director of UConn’s Institute for Systems Genomics. “Also,
thanks to the investments in genomics through the University’s Academic Plan,
Brent Graveley can leverage his expertise so that faculty and students across
our campuses will successfully compete for grant dollars and launch bioscience
ventures.”
Graveley will speak about the research at the Oxford
Nanopore MinION Community Meeting at the New York Genome
Center
As for next steps, the researchers plan on going even
bigger: sequencing every bit of RNA from beginning to end inside a single cell,
something that cannot be done with traditional gene sequencers.
“This technology has amazing potential to transform how we study RNA biology and the type of information we can obtain,” says Graveley. “Plus the fact that the MinION is a hand-held sequencer that you plug into a laptop is simply unbelievably cool!”
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