Cargando…

Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD

INTRODUCTION: The most common forms of amyotrophic lateral sclerosis and frontotemporal dementia are caused by a large GGGGCC repeat expansion in the first intron of the C9orf72 gene. The repeat-containing intron should be degraded after being spliced out, however GGGGCC repeat-containing RNA specie...

Descripción completa

Detalles Bibliográficos
Autores principales: Niblock, Michael, Smith, Bradley N., Lee, Youn-Bok, Sardone, Valentina, Topp, Simon, Troakes, Claire, Al-Sarraj, Safa, Leblond, Claire S., Dion, Patrick A., Rouleau, Guy A., Shaw, Christopher E., Gallo, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766718/
https://www.ncbi.nlm.nih.gov/pubmed/26916632
http://dx.doi.org/10.1186/s40478-016-0289-4
_version_ 1782417719078944768
author Niblock, Michael
Smith, Bradley N.
Lee, Youn-Bok
Sardone, Valentina
Topp, Simon
Troakes, Claire
Al-Sarraj, Safa
Leblond, Claire S.
Dion, Patrick A.
Rouleau, Guy A.
Shaw, Christopher E.
Gallo, Jean-Marc
author_facet Niblock, Michael
Smith, Bradley N.
Lee, Youn-Bok
Sardone, Valentina
Topp, Simon
Troakes, Claire
Al-Sarraj, Safa
Leblond, Claire S.
Dion, Patrick A.
Rouleau, Guy A.
Shaw, Christopher E.
Gallo, Jean-Marc
author_sort Niblock, Michael
collection PubMed
description INTRODUCTION: The most common forms of amyotrophic lateral sclerosis and frontotemporal dementia are caused by a large GGGGCC repeat expansion in the first intron of the C9orf72 gene. The repeat-containing intron should be degraded after being spliced out, however GGGGCC repeat-containing RNA species either accumulate in nuclear foci or are exported to the cytoplasm where they are translated into potentially toxic dipeptide repeat proteins by repeat-associated non-AUG-initiated (RAN) translation. RESULTS: In order to determine the mechanisms of repeat-containing intron misprocessing, we have analyzed C9orf72 transcripts in lymphoblasts from C9orf72 expansion carriers (n = 15) and control individuals (n = 15). We have identified polyadenylated C9orf72 RNA species retaining the repeat-containing intron and in which downstream exons are spliced correctly resulting in a C9orf72 mRNA with an enlarged 5’-UTR containing the GGGGCC repeats. Intron-retaining transcripts are produced from both wild-type and mutant alleles. Intron-retaining C9orf72 transcripts were also detected in brain with a 2.7 fold increase measured in the frontal cortex from heterozygous expansion carriers (n = 11) compared to controls (n = 10). The level of intron-retaining transcripts was increased 5.9 fold in a case homozygous for the expansion. We also show that a large proportion of intron 1-retaining C9orf72 transcripts accumulate in the nucleus. CONCLUSIONS: Retention of the repeat-containing intron in mature C9orf72 mRNA can potentially explain nuclear foci formation as well as nuclear export of GGGGCC repeat RNA and suggests that the misprocessing of C9orf72 transcripts initiates the pathogenic process caused by C9orf72 hexanucleotide repeat expansions as well as provides the basis for novel therapeutic strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-016-0289-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4766718
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47667182016-02-26 Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD Niblock, Michael Smith, Bradley N. Lee, Youn-Bok Sardone, Valentina Topp, Simon Troakes, Claire Al-Sarraj, Safa Leblond, Claire S. Dion, Patrick A. Rouleau, Guy A. Shaw, Christopher E. Gallo, Jean-Marc Acta Neuropathol Commun Research INTRODUCTION: The most common forms of amyotrophic lateral sclerosis and frontotemporal dementia are caused by a large GGGGCC repeat expansion in the first intron of the C9orf72 gene. The repeat-containing intron should be degraded after being spliced out, however GGGGCC repeat-containing RNA species either accumulate in nuclear foci or are exported to the cytoplasm where they are translated into potentially toxic dipeptide repeat proteins by repeat-associated non-AUG-initiated (RAN) translation. RESULTS: In order to determine the mechanisms of repeat-containing intron misprocessing, we have analyzed C9orf72 transcripts in lymphoblasts from C9orf72 expansion carriers (n = 15) and control individuals (n = 15). We have identified polyadenylated C9orf72 RNA species retaining the repeat-containing intron and in which downstream exons are spliced correctly resulting in a C9orf72 mRNA with an enlarged 5’-UTR containing the GGGGCC repeats. Intron-retaining transcripts are produced from both wild-type and mutant alleles. Intron-retaining C9orf72 transcripts were also detected in brain with a 2.7 fold increase measured in the frontal cortex from heterozygous expansion carriers (n = 11) compared to controls (n = 10). The level of intron-retaining transcripts was increased 5.9 fold in a case homozygous for the expansion. We also show that a large proportion of intron 1-retaining C9orf72 transcripts accumulate in the nucleus. CONCLUSIONS: Retention of the repeat-containing intron in mature C9orf72 mRNA can potentially explain nuclear foci formation as well as nuclear export of GGGGCC repeat RNA and suggests that the misprocessing of C9orf72 transcripts initiates the pathogenic process caused by C9orf72 hexanucleotide repeat expansions as well as provides the basis for novel therapeutic strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-016-0289-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-25 /pmc/articles/PMC4766718/ /pubmed/26916632 http://dx.doi.org/10.1186/s40478-016-0289-4 Text en © Niblock et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Niblock, Michael
Smith, Bradley N.
Lee, Youn-Bok
Sardone, Valentina
Topp, Simon
Troakes, Claire
Al-Sarraj, Safa
Leblond, Claire S.
Dion, Patrick A.
Rouleau, Guy A.
Shaw, Christopher E.
Gallo, Jean-Marc
Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title_full Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title_fullStr Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title_full_unstemmed Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title_short Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
title_sort retention of hexanucleotide repeat-containing intron in c9orf72 mrna: implications for the pathogenesis of als/ftd
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766718/
https://www.ncbi.nlm.nih.gov/pubmed/26916632
http://dx.doi.org/10.1186/s40478-016-0289-4
work_keys_str_mv AT niblockmichael retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT smithbradleyn retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT leeyounbok retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT sardonevalentina retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT toppsimon retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT troakesclaire retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT alsarrajsafa retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT leblondclaires retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT dionpatricka retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT rouleauguya retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT shawchristophere retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd
AT gallojeanmarc retentionofhexanucleotiderepeatcontainingintroninc9orf72mrnaimplicationsforthepathogenesisofalsftd