This
is the first time that an entire newt genome has been sequenced, an achievement
that can give rise to new discoveries on the amphibian’s ability to recreate
brain neurons as well as entire body parts. Amongst the first findings are a
multitude of copies of a certain microRNA group, which in mammals is mainly
found in embryonic stem cells, but also in tumour cells.
Resistant to tumour formation
“It
will be exciting to figure out how regeneration in the adult organism
re-activates embryonic genes,” says study leader Professor András Simon at
Karolinska Institutet’s Department of Cell and Molecular Biology. “What’s needed now are functional
studies of these microRNA molecules to understand their function in
regeneration. The link to cancer cells is also very interesting, especially
bearing in mind newts’ marked resistance to tumour formation.”
Even
though the abundance of stem cell microRNA genes is quite surprising, it alone
cannot explain how salamanders regenerate so well. Professor Simon predicts
that the explanation lies in a combination of genes unique to salamanders and
how other more common genes orchestrate and control the actual regeneration
process.
Technical and methodological challenge
One
of the reasons why salamander genomes have not been sequenced before is its
sheer size – six times bigger than the human genome in the case of the Iberian
newt, which has posed an enormous technical and methodological challenge.
“It’s
only now that the technology is available to handle such a large genome,” says
Professor Simon. “The sequencing per se doesn’t take that long – it’s
recreating the genome from the sequences that’s so time consuming.”
“We
all realised how challenging it was going to be,” recounts first author Ahmed Elewa,
postdoctoral fellow at the same department. “But the very fact that it was such
a challenge made it all the more exciting.”
Can recreate cells that die in Parkinson’s disease
The
group at Karolinska Institutet is now engaging with other researchers to
discover what can be learned from the newt genome and test new hypotheses
through systematic comparisons with mammals.
“We
showed ten years ago that salamanders can recreate all the cells that die in
Parkinson’s disease in the space of four weeks,” says Professor Simon. “We can
now delve deeply into the molecular processes underlying this ability. Although
we’re doing basic research, our findings can hopefully lead to the development
of new regenerative strategies for humans.”
The
sequencing project was conducted in collaboration with SciLifeLab and Uppsala
University and was largely financed with grants from the Swedish Research
Council, the National Institutes of Health (USA), the European Research
Council, the Swedish Cancer Society and the Wenner-Gren Foundation.
Publication
“Reading
and editing the Pleurodeles waltl genome reveals novel features of tetrapod
regeneration”
Ahmed Elewa, Heng Wang, Carlos Talavera-López, Alberto Joven, Gonçalo Brito,
Anoop Kumar, L Shahul Hameed, May Penrad-Mobayed, Zeyu Yao, Neda Zamani, Yamen
Abbas, Ilgar Abdullayev, Rickard Sandberg, Manfred Grabherr, Björn Andersson,
András Simon
Nature Communications, online 22 December 2017, doi:
10.1038/s41467-017-01964-9
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