Correlation Engine 2.0
Clear Search sequence regions


  • basal ganglia (1)
  • brain (2)
  • CAG (3)
  • disease and (3)
  • dystonia (4)
  • factor (8)
  • HTT (1)
  • human cells (1)
  • humans (1)
  • huntington disease (11)
  • mice (8)
  • neuroblastoma (1)
  • pathogenesis (1)
  • patients (1)
  • phosphoproteins (2)
  • protein family (1)
  • protein human (2)
  • retrotransposon (1)
  • rich (2)
  • rna (4)
  • sr protein (2)
  • TAF1 (11)
  • TATA (3)
  • toxic (1)
  • Sizes of these terms reflect their relevance to your search.

    Huntington's disease and X-linked dystonia parkinsonism are two monogenic basal ganglia model diseases. Huntington's disease is caused by a polyglutamine-encoding CAG repeat expansion in the Huntingtin (HTT) gene leading to several toxic interactions of both the expanded CAG-containing mRNA and the polyglutamine-containing protein, while X-linked dystonia parkinsonism is caused by a retrotransposon insertion in the TAF1 gene, which decreases expression of this core scaffold of the basal transcription factor complex TFIID. SRSF6 is an RNA-binding protein of the serine and arginine-rich (SR) protein family that interacts with expanded CAG mRNA and is sequestered into the characteristic polyglutamine-containing inclusion bodies of Huntington's disease brains. Here we report decreased levels of the SRSF6 interactor and regulator SREK1-another SR protein involved in RNA processing-which includes TAF1 as one of its targets. This led us to hypothesize that Huntington's disease and X-linked dystonia parkinsonism pathogeneses converge in TAF1 alteration. We show that diminishing SRSF6 through RNA interference in human neuroblastoma cells leads to a decrease in SREK1 levels, which, in turn, suffices to cause diminished TAF1 levels. We also observed decreased SREK1 and TAF1 levels in striatum of Huntington's disease patients and transgenic model mice. We then generated mice with neuronal transgenic expression of SREK1 (TgSREK1 mice) that, interestingly, showed transcriptomic alterations complementary to those in Huntington's disease mice. Most importantly, by combining Huntington's disease and TgSREK1 mice we verify that SREK1 overexpression corrects TAF1 deficiency and attenuates striatal atrophy and motor phenotype of Huntington's disease mice. Our results therefore demonstrate that altered RNA processing upon SREK1 dysregulation plays a key role in Huntington's disease pathogenesis and pinpoint TAF1 as a likely general determinant of selective vulnerability of the striatum in multiple neurological disorders. © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain.

    Citation

    Ivó H Hernández, Jorge R Cabrera, María Santos-Galindo, Manuel Sánchez-Martín, Verónica Domínguez, Ramón García-Escudero, María J Pérez-Álvarez, Belén Pintado, José J Lucas. Pathogenic SREK1 decrease in Huntington's disease lowers TAF1 mimicking X-linked dystonia parkinsonism. Brain : a journal of neurology. 2020 Jul 01;143(7):2207-2219

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 32533168

    View Full Text