Discovery of a new ALS and dementia disease mechanism raises treatment
hopes
Date:
February 23, 2022
Source:
University College London
Summary:
A pioneering new study has revealed, for the first time, why a
common genetic variant worsens disease outcomes for people with
the devastating adult-onset neurodegenerative diseases amyotrophic
lateral sclerosis (ALS) and frontotemporal dementia (FTD).
FULL STORY ==========================================================================
A pioneering new study led by UCL and National Institutes of Health (NIH) scientists has revealed, for the first time, why a common genetic variant worsens disease outcomes for people with the devastating adult-onset neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).
========================================================================== Published in Nature, the study shows how TDP-43 protein depletion,
associated with almost all cases (97%) of ALS and half of FTD cases,
corrupts the genetic instructions for the critical neuronal protein
UNC13A.
Strikingly, it found that a mysterious genetic variant previously
associated with disease risk increases the chance of UNC13A's genetic instructions being corrupted among people with the diseases, thereby
worsening risk and severity of ALS and FTD.
UNC13A enables neurons (nerve cells) to communicate with each other via neurotransmitter release, and data from animal models suggests its loss
from neurons can be fatal. The researchers believe that the corruption
of UNC13A's genetic instructions in patients may have similarly harmful consequences.
ALS is the most common motor neuron disease and there is no known cure;
it affects the brain and spinal cord by attacking the neurons and nerves
which control movement, causing them to die. There is currently only one approved drug for ALS in the UK, which extends lifespan by a few months,
and is only effective for a tiny minority of patients. One third of
patients die within one year of diagnosis.
FTD is a related disease with similar underlying causes; symptoms include language impairment, changes in personality and cognitive difficulties.
========================================================================== Researchers say the discovery raises hope for new treatments; by
developing a therapy that blocks the corruption of UNC13A's genetic instructions, disease progression could be slowed for most people with
ALS and around half of patients with FTD.
Corresponding author Professor Pietro Fratta (UCL Queen Square Institute
of Neurology) said: "The majority of research into gene therapy has
focused on genes implicated in familial ALS (patients with a family
history of the disease), but the vast majority of ALS cases are sporadic,
with no known family history." Co-corresponding author Dr Michael Ward (National Institute of Neurological Disorders and Stroke, NIH, US) added:
"We have known for a long time that genetic variants in UNC13A cause an increased risk of ALS and dementia, but nobody had figured out why this
is the case. Together, our teams showed exactly how this genetic risk
factor for ALS interplays with the core disease mechanism, TDP-43 loss,
in order to worsen the disease course." TDP-43 -- a key player in ALS
and FTD Arguably the most important protein in ALS research is TDP-43, as
in most cases (as well as half of FTD cases), the protein is incorrectly ejected from the cell's nucleus. This prevents TDP-43 from performing
its important functions, such as ensuring that mRNA is produced correctly.
==========================================================================
Dr Ward said: "We have known for a long time that most patients with ALS,
and about half of FTD patients, lose the function of a key protein called TDP-43, wreaking havoc in nerve cells that are affected. But we haven't
known how to reverse the most problematic consequences of TDP-43 loss."
As part of the experimental study, the researchers used skin-derived
human stem cells to make neuronal cells in dishes and removed the TDP-43 protein from these cells using a new technology based on CRISPR-Cas9,
the Nobel-prize winning gene-editing technology.
The scientists were then able to study how these neurons without TDP-43 differed from healthy neurons. They found that the mRNAs for the UNC13A
protein were corrupted, meaning the ribosomes in the lab-grown neurons
were unable to correctly produce the UNC13A protein. Furthermore,
when the team looked at ALS and FTD patient brain samples, they again
found that the mRNAs for UNC13A were incorrect, confirming that their experiments replicated the real-world disease process.
Given the essential role UNC13A plays in facilitating neuron
communication, its corruption is thus likely to impair neuronal function
and contribute to neurodegeneration in those with ALS and FTD.
Genetic variants increase the risk of UNC13A mRNA corruption The UNC13A
gene and its corresponding protein are of longstanding interest to
motor neuron disease and FTD researchers, with previous studies showing
common genetic variants increase the risk and severity of the diseases,
despite being benign in most people unaffected by the diseases (half
the population carries one of these variants, which are only harmful in
people with ALS or FTD).
However, despite over a decade of research, the exact reason for this
has remained mysterious, as these variants do not directly alter the
UNC13A protein-coding sequence, but are instead located in a region of
'junk DNA'.
The researchers believe they have uncovered the answer to this critical question: they found that the risk-linked variants greatly increase the
chance of the UNC13A mRNA becoming corrupted once the ALS and FTD disease course, and the associated loss of TDP-43 protein, has begun. Thus,
patients with these genetic variants are likely to suffer greater loss
of UNC13A, resulting in more severe disease.
Co-lead author, PhD student Oscar Wilkins (UCL Queen Square Institute of Neurology and Francis Crick Institute), said: "These results represent
a significant breakthrough for several reasons. Firstly, they explain
why UNC13A genetic variants increase the risk of motor neuron disease and dementia, a question which has puzzled researchers for over a decade. They
are also the first to demonstrate a genetic link specifically between loss
of nuclear TDP-43 function and ALS, improving scientific understanding
of this central disease mechanism." Next steps Professor Fratta said:
"We have built on years of genetic research that identified that UNC13A
was implicated in motor neuron disease and FTD, and supported it with a
new molecular biology finding that confirms that the gene is absolutely fundamental to the disease process.
"We are hoping to carry out trials over the coming years to develop
such a treatment that could potentially greatly improve the lives of
people living with ALS." The researchers are confident that with this
new information, new therapies for motor neuron disease can be created
that stop UNC13A mRNAs from being corrupted in patients.
The study involved researchers at UCL, NIH, the Crick, New York Genome
Center, Mount Sinai, International Centre for Genetic Engineering and Biotechnology, and the National Institute of Chemistry (Slovenia). The
study was funded by the Medical Research Council and the Motor Neurone
Disease Association and the NIH with support from Rosetrees Trust,
The Robert Packard Center for ALS Research, Wellcome, Collaborative
Centre for Applied Nanotechnology and Collaborative Center for X-linked Dystonia-Parkinsonism.
special promotion Explore the latest scientific research on sleep and
dreams in this free online course from New Scientist -- Sign_up_now_>>> ========================================================================== Story Source: Materials provided by University_College_London. Note:
Content may be edited for style and length.
========================================================================== Journal Reference:
1. Anna-Leigh Brown, Oscar G. Wilkins, Matthew J. Keuss, Sarah E. Hill,
Matteo Zanovello, Weaverly Colleen Lee, Alexander Bampton, Flora
C. Y.
Lee, Laura Masino, Yue A. Qi, Sam Bryce-Smith, Ariana Gatt, Martina
Hallegger, Delphine Fagegaltier, Hemali Phatnani, Hemali Phatnani,
Justin Kwan, Dhruv Sareen, James R. Broach, Zachary Simmons,
Ximena Arcila- Londono, Edward B. Lee, Vivianna M. Van Deerlin,
Neil A. Shneider, Ernest Fraenkel, Lyle W. Ostrow, Frank Baas,
Noah Zaitlen, James D. Berry, Andrea Malaspina, Pietro Fratta,
Gregory A. Cox, Leslie M. Thompson, Steve Finkbeiner, Efthimios
Dardiotis, Timothy M. Miller, Siddharthan Chandran, Suvankar Pal,
Eran Hornstein, Daniel J. MacGowan, Terry Heiman- Patterson, Molly
G. Hammell, Nikolaos. A. Patsopoulos, Oleg Butovsky, Joshua Dubnau,
Avindra Nath, Robert Bowser, Matthew Harms, Eleonora Aronica,
Mary Poss, Jennifer Phillips-Cremins, John Crary, Nazem Atassi,
Dale J. Lange, Darius J. Adams, Leonidas Stefanis, Marc Gotkine,
Robert H. Baloh, Suma Babu, Towfique Raj, Sabrina Paganoni, Ophir
Shalem, Colin Smith, Bin Zhang, Brent Harris, Iris Broce, Vivian
Drory, John Ravits, Corey McMillan, Vilas Menon, Lani Wu, Steven
Altschuler, Yossef Lerner, Rita Sattler, Kendall Van Keuren-Jensen,
Orit Rozenblatt-Rosen, Kerstin Lindblad-Toh, Katharine Nicholson,
Peter Gregersen, Jeong-Ho Lee, Sulev Kokos, Stephen Muljo, Jia
Newcombe, Emil K. Gustavsson, Sahba Seddighi, Joel F. Reyes,
Steven L. Coon, Daniel Ramos, Giampietro Schiavo, Elizabeth
M. C. Fisher, Towfique Raj, Maria Secrier, Tammaryn Lashley,
Jernej Ule, Emanuele Buratti, Jack Humphrey, Michael E. Ward,
Pietro Fratta. TDP-43 loss and ALS-risk SNPs drive mis-splicing and
depletion of UNC13A. Nature, 2022; DOI: 10.1038/s41586-022-04436-3 ==========================================================================
Link to news story:
https://www.sciencedaily.com/releases/2022/02/220223111310.htm
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