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Widespread alterations in microRNA biogenesis in human Huntington’s disease putamen

Petry, Serena (author)
Laval University
Keraudren, Rémi (author)
Laval University
Nateghi, Behnaz (author)
Laval University
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Loiselle, Andréanne (author)
Laval University
Pircs, Karolina (author)
Lund University,Lunds universitet,Molekylär neurogenetik,Forskargrupper vid Lunds universitet,Molecular Neurogenetics,Lund University Research Groups,Semmelweis University
Jakobsson, Johan (author)
Lund University,Lunds universitet,Molekylär neurogenetik,Forskargrupper vid Lunds universitet,Molecular Neurogenetics,Lund University Research Groups
Sephton, Chantelle (author)
Laval University
Langlois, Mélanie (author)
Laval University,Centre hospitalier universitaire de Québec
St-Amour, Isabelle (author)
Laval University
Hébert, Sébastien S. (author)
Laval University
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 (creator_code:org_t)
2022-07-22
2022
English.
In: Acta Neuropathologica Communications. - : Springer Science and Business Media LLC. - 2051-5960. ; 10
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Altered microRNA (miRNA) expression is a common feature of Huntington’s disease (HD) and could participate in disease onset and progression. However, little is known about the underlying causes of miRNA disruption in HD. We and others have previously shown that mutant Huntingtin binds to Ago2, a central component of miRNA biogenesis, and disrupts mature miRNA levels. In this study, we sought to determine if miRNA maturation per se was compromised in HD. Towards this end, we characterized major miRNA biogenesis pathway components and miRNA maturation products (pri-miRNA, pre-miRNA, and mature) in human HD (N = 41, Vonsattel grades HD2-4) and healthy control (N = 25) subjects. Notably, the striatum (putamen) and cortex (BA39) from the same individuals were analyzed in parallel. We show that Ago2, Drosha, and Dicer were strongly downregulated in human HD at the early stages of the disease. Using a panel of HD-related miRNAs (miR-10b, miR-196b, miR-132, miR-212, miR-127, miR-128), we uncovered various types of maturation defects in the HD brain, the most prominent occurring at the pre-miRNA to mature miRNA maturation step. Consistent with earlier findings, we provide evidence that alterations in autophagy could participate in miRNA maturation defects. Notably, most changes occurred in the striatum, which is more prone to HTT aggregation and neurodegeneration. Likewise, we observed no significant alterations in miRNA biogenesis in human HD cortex and blood, strengthening tissue-specific effects. Overall, these data provide important clues into the underlying mechanisms behind miRNA alterations in HD-susceptible tissues. Further investigations are now required to understand the biological, diagnostic, and therapeutic implications of miRNA/RNAi biogenesis defects in HD and related neurodegenerative disorders.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

Ago2
Autophagy
Biogenesis
Dicer
Huntington’s disease
microRNA
RNAi

Publication and Content Type

art (subject category)
ref (subject category)

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