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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein
To discover novel genes underlying amyotrophic lateral sclerosis (ALS), we aggregated exomes from 3,864 cases and 7,839 ancestry-matched controls. We observed a significant excess of rare protein-truncating variants among ALS cases, and these variants were concentrated in constrained genes. Through gene level analyses, we replicated known ALS genes including SOD1, NEK1 and FUS. We also observed multiple distinct protein-truncating variants in a highly constrained gene, DNAJC7. The signal in DNAJC7 exceeded genome-wide significance, and immunoblotting assays showed depletion of DNAJC7 protein in fibroblasts in a patient with ALS carrying the p.Arg156Ter variant. DNAJC7 encodes a member of the heat-shock protein family, HSP40, which, along with HSP70 proteins, facilitates protein homeostasis, including folding of newly synthesized polypeptides and clearance of degraded proteins. When these processes are not regulated, misfolding and accumulation of aberrant proteins can occur and lead to protein aggregation, which is a pathological hallmark of neurodegeneration. Our results highlight DNAJC7 as a novel gene for ALS.
1097-6256
1966-1974
Farhan, Sali M. K.
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Howrigan, Daniel P.
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Abbott, Liam E.
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Klim, Joseph R.
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Topp, Simon D.
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Byrnes, Andrea E.
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Churchhouse, Claire
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Phatnani, Hemali
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Smith, Bradley N.
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Wuu, Joanne
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Shatunov, Aleksey
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Iacoangeli, Alfredo
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Ghosh, Sulagna
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Eggan, Kevin
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Rademakers, Rosa
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Mccauley, Jacob L.
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Schüle, Rebecca
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Züchner, Stephan
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Morrison, Karen E.
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Al-chalabi, Ammar
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Traynor, Bryan
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Shaw, Christopher E.
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Goldstein, David B.
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Daly, Mark J.
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Neale, Benjamin M.
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Farhan, Sali M. K.
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Topp, Simon D.
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Churchhouse, Claire
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Phatnani, Hemali
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Smith, Bradley N.
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Wu, Gang
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Wuu, Joanne
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Shatunov, Aleksey
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Iacoangeli, Alfredo
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Al Khleifat, Ahmad
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Mordes, Daniel A.
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Ghosh, Sulagna
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Eggan, Kevin
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Rademakers, Rosa
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Mccauley, Jacob L.
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Schüle, Rebecca
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Züchner, Stephan
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Gotkine, Marc
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Morrison, Karen E.
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Al-chalabi, Ammar
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Traynor, Bryan
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Shaw, Christopher E.
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Goldstein, David B.
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Harms, Matthew B.
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Daly, Mark J.
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Neale, Benjamin M.
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Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, Mccauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J. and Neale, Benjamin M. (2019) Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience, 22 (12), 1966-1974. (doi:10.1038/s41593-019-0530-0).

Record type: Article

Abstract

To discover novel genes underlying amyotrophic lateral sclerosis (ALS), we aggregated exomes from 3,864 cases and 7,839 ancestry-matched controls. We observed a significant excess of rare protein-truncating variants among ALS cases, and these variants were concentrated in constrained genes. Through gene level analyses, we replicated known ALS genes including SOD1, NEK1 and FUS. We also observed multiple distinct protein-truncating variants in a highly constrained gene, DNAJC7. The signal in DNAJC7 exceeded genome-wide significance, and immunoblotting assays showed depletion of DNAJC7 protein in fibroblasts in a patient with ALS carrying the p.Arg156Ter variant. DNAJC7 encodes a member of the heat-shock protein family, HSP40, which, along with HSP70 proteins, facilitates protein homeostasis, including folding of newly synthesized polypeptides and clearance of degraded proteins. When these processes are not regulated, misfolding and accumulation of aberrant proteins can occur and lead to protein aggregation, which is a pathological hallmark of neurodegeneration. Our results highlight DNAJC7 as a novel gene for ALS.

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More information

Accepted/In Press date: 2 October 2019
e-pub ahead of print date: 25 November 2019

Identifiers

Local EPrints ID: 436371
URI: http://eprints.soton.ac.uk/id/eprint/436371
ISSN: 1097-6256
PURE UUID: 93297fbf-7977-4440-9ebd-cbb41a05ae80
ORCID for Karen E. Morrison: ORCID iD orcid.org/0000-0003-0216-5717

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Date deposited: 09 Dec 2019 17:30
Last modified: 16 Mar 2024 05:37

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Contributors

Author: Sali M. K. Farhan
Author: Daniel P. Howrigan
Author: Liam E. Abbott
Author: Joseph R. Klim
Author: Simon D. Topp
Author: Andrea E. Byrnes
Author: Claire Churchhouse
Author: Hemali Phatnani
Author: Bradley N. Smith
Author: Evadnie Rampersaud
Author: Gang Wu
Author: Joanne Wuu
Author: Aleksey Shatunov
Author: Alfredo Iacoangeli
Author: Ahmad Al Khleifat
Author: Daniel A. Mordes
Author: Sulagna Ghosh
Author: Kevin Eggan
Author: Rosa Rademakers
Author: Jacob L. Mccauley
Author: Rebecca Schüle
Author: Stephan Züchner
Author: Michael Benatar
Author: J. Paul Taylor
Author: Michael Nalls
Author: Marc Gotkine
Author: Pamela J. Shaw
Author: Karen E. Morrison ORCID iD
Author: Ammar Al-chalabi
Author: Bryan Traynor
Author: Christopher E. Shaw
Author: David B. Goldstein
Author: Matthew B. Harms
Author: Mark J. Daly
Author: Benjamin M. Neale

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