Identification of cyclin D1 as a major modulator of 3-nitropropionic acid-induced striatal neurodegeneration

• Published in: Neurobiology of disease 2022-01, Vol.162, p.105581-105581, Article 105581
• Main Authors: Dietrich, Paula, Alli, Shanta, Mulligan, Megan K., Cox, Rachel, Ashbrook, David G., Williams, Robert W., Dragatsis, Ioannis
• Format: Article
• Language: English
• Subjects: 3-Nitropropionic acid; BXD; Cell cycle; Corpus Striatum - metabolism; Cyclin D1; Cyclin D1 - genetics; Cyclin D1 - metabolism; Mouse; Neurodegeneration; Nitro Compounds - metabolism; Nitro Compounds - toxicity; Propionates - metabolism; Propionates - toxicity; Striatum
• ISSN: 0969-9961; 1095-953X
• DOI: 10.1016/j.nbd.2021.105581

Mitochondria dysfunction occurs in the aging brain as well as in several neurodegenerative disorders and predisposes neuronal cells to enhanced sensitivity to neurotoxins. 3-nitropropionic acid (3-NP) is a naturally occurring plant and fungal neurotoxin that causes neurodegeneration predominantly in the striatum by irreversibly inhibiting the tricarboxylic acid respiratory chain enzyme, succinate dehydrogenase (SDH), the main constituent of the mitochondria respiratory chain complex II. Significantly, although 3-NP-induced inhibition of SDH occurs in all brain regions, neurodegeneration occurs primarily and almost exclusively in the striatum for reasons still not understood. In rodents, 3-NP-induced striatal neurodegeneration depends on the strain background suggesting that genetic differences among genotypes modulate toxicant variability and mechanisms that underlie 3-NP-induced neuronal cell death. Using the large BXD family of recombinant inbred (RI) strains we demonstrate that variants in Ccnd1 - the gene encoding cyclin D1 - of the DBA/2 J parent underlie the resistance to 3-NP-induced striatal neurodegeneration. In contrast, the Ccnd1 variant inherited from the widely used C57BL/6 J parental strain confers sensitivity. Given that cellular stress triggers induction of cyclin D1 expression followed by cell-cycle re-entry and consequent neuronal cell death, we sought to determine if the C57BL/6 J and DBA/2 J Ccnd1 variants are differentially modulated in response to 3-NP. We confirm that 3-NP induces cyclin D1 expression in striatal neuronal cells of C57BL/6 J, but this response is blunted in the DBA/2 J. We further show that striatal-specific alternative processing of a highly conserved 3′UTR negative regulatory region of Ccnd1 co-segregates with the C57BL/6 J parental Ccnd1 allele in BXD strains and that its differential processing accounts for sensitivity or resistance to 3-NP. Our results indicate that naturally occurring Ccnd1 variants may play a role in the variability observed in neurodegenerative disorders involving mitochondria complex II dysfunction and point to cyclin D1 as a possible therapeutic target. •3-Nitropropionic acid (3-NP) induces striatal lesions in C57BL/6 J (B6) but not in DBA/2 J (D2) mice.•Forward genetics identified Ccnd1 (cyclin D1) as a strong candidate for strain-specific 3-NP response.•3-NP induces cyclin D1 expression in B6 striatum but not in D2.•Ccnd1 mRNA's 3′UTR is alternatively processed in B6 striatum.•Alternative