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Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease

SORL1 is strongly associated with both sporadic and familial forms of Alzheimer’s disease (AD), but a lack of information about alternatively spliced transcripts currently limits our understanding of the role of SORL1 in AD. Here, we describe a SORL1 transcript (SORL1-38b) characterized by inclusion...

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Autores principales: Monti, Giulia, Kjolby, Mads, Jensen, Anne Mette G., Allen, Mariet, Reiche, Juliane, Møller, Peter L., Comaposada-Baró, Raquel, Zolkowski, Bartlomiej E., Vieira, Cármen, Jørgensen, Margarita Melnikova, Holm, Ida E., Valdmanis, Paul N., Wellner, Niels, Vægter, Christian B., Lincoln, Sarah J., Nykjær, Anders, Ertekin-Taner, Nilüfer, Young, Jessica E., Nyegaard, Mette, Andersen, Olav M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962264/
https://www.ncbi.nlm.nih.gov/pubmed/33726851
http://dx.doi.org/10.1186/s40478-021-01140-7
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author Monti, Giulia
Kjolby, Mads
Jensen, Anne Mette G.
Allen, Mariet
Reiche, Juliane
Møller, Peter L.
Comaposada-Baró, Raquel
Zolkowski, Bartlomiej E.
Vieira, Cármen
Jørgensen, Margarita Melnikova
Holm, Ida E.
Valdmanis, Paul N.
Wellner, Niels
Vægter, Christian B.
Lincoln, Sarah J.
Nykjær, Anders
Ertekin-Taner, Nilüfer
Young, Jessica E.
Nyegaard, Mette
Andersen, Olav M.
author_facet Monti, Giulia
Kjolby, Mads
Jensen, Anne Mette G.
Allen, Mariet
Reiche, Juliane
Møller, Peter L.
Comaposada-Baró, Raquel
Zolkowski, Bartlomiej E.
Vieira, Cármen
Jørgensen, Margarita Melnikova
Holm, Ida E.
Valdmanis, Paul N.
Wellner, Niels
Vægter, Christian B.
Lincoln, Sarah J.
Nykjær, Anders
Ertekin-Taner, Nilüfer
Young, Jessica E.
Nyegaard, Mette
Andersen, Olav M.
author_sort Monti, Giulia
collection PubMed
description SORL1 is strongly associated with both sporadic and familial forms of Alzheimer’s disease (AD), but a lack of information about alternatively spliced transcripts currently limits our understanding of the role of SORL1 in AD. Here, we describe a SORL1 transcript (SORL1-38b) characterized by inclusion of a novel exon (E38b) that encodes a truncated protein. We identified E38b-containing transcripts in several brain regions, with the highest expression in the cerebellum and showed that SORL1-38b is largely located in neuronal dendrites, which is in contrast to the somatic distribution of transcripts encoding the full-length SORLA protein (SORL1-fl). SORL1-38b transcript levels were significantly reduced in AD cerebellum in three independent cohorts of postmortem brains, whereas no changes were observed for SORL1-fl. A trend of lower 38b transcript level in cerebellum was found for individuals carrying the risk variant at rs2282649 (known as SNP24), although not reaching statistical significance. These findings suggest synaptic functions for SORL1-38b in the brain, uncovering novel aspects of SORL1 that can be further explored in AD research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01140-7.
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spelling pubmed-79622642021-03-16 Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease Monti, Giulia Kjolby, Mads Jensen, Anne Mette G. Allen, Mariet Reiche, Juliane Møller, Peter L. Comaposada-Baró, Raquel Zolkowski, Bartlomiej E. Vieira, Cármen Jørgensen, Margarita Melnikova Holm, Ida E. Valdmanis, Paul N. Wellner, Niels Vægter, Christian B. Lincoln, Sarah J. Nykjær, Anders Ertekin-Taner, Nilüfer Young, Jessica E. Nyegaard, Mette Andersen, Olav M. Acta Neuropathol Commun Research SORL1 is strongly associated with both sporadic and familial forms of Alzheimer’s disease (AD), but a lack of information about alternatively spliced transcripts currently limits our understanding of the role of SORL1 in AD. Here, we describe a SORL1 transcript (SORL1-38b) characterized by inclusion of a novel exon (E38b) that encodes a truncated protein. We identified E38b-containing transcripts in several brain regions, with the highest expression in the cerebellum and showed that SORL1-38b is largely located in neuronal dendrites, which is in contrast to the somatic distribution of transcripts encoding the full-length SORLA protein (SORL1-fl). SORL1-38b transcript levels were significantly reduced in AD cerebellum in three independent cohorts of postmortem brains, whereas no changes were observed for SORL1-fl. A trend of lower 38b transcript level in cerebellum was found for individuals carrying the risk variant at rs2282649 (known as SNP24), although not reaching statistical significance. These findings suggest synaptic functions for SORL1-38b in the brain, uncovering novel aspects of SORL1 that can be further explored in AD research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01140-7. BioMed Central 2021-03-16 /pmc/articles/PMC7962264/ /pubmed/33726851 http://dx.doi.org/10.1186/s40478-021-01140-7 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Monti, Giulia
Kjolby, Mads
Jensen, Anne Mette G.
Allen, Mariet
Reiche, Juliane
Møller, Peter L.
Comaposada-Baró, Raquel
Zolkowski, Bartlomiej E.
Vieira, Cármen
Jørgensen, Margarita Melnikova
Holm, Ida E.
Valdmanis, Paul N.
Wellner, Niels
Vægter, Christian B.
Lincoln, Sarah J.
Nykjær, Anders
Ertekin-Taner, Nilüfer
Young, Jessica E.
Nyegaard, Mette
Andersen, Olav M.
Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title_full Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title_fullStr Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title_full_unstemmed Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title_short Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease
title_sort expression of an alternatively spliced variant of sorl1 in neuronal dendrites is decreased in patients with alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962264/
https://www.ncbi.nlm.nih.gov/pubmed/33726851
http://dx.doi.org/10.1186/s40478-021-01140-7
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