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  1. Article ; Online: Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes

    James N. Sleigh / Andrew P. Tosolini / David Gordon / Anny Devoy / Pietro Fratta / Elizabeth M.C. Fisher / Kevin Talbot / Giampietro Schiavo

    Cell Reports, Vol 30, Iss 11, Pp 3655-3662.e

    2020  Volume 2

    Abstract: Summary: Amyotrophic lateral sclerosis (ALS) is a fatal, progressive neurodegenerative disease resulting from a complex interplay between genetics and environment. Impairments in axonal transport have been identified in several ALS models, but in vivo ... ...

    Abstract Summary: Amyotrophic lateral sclerosis (ALS) is a fatal, progressive neurodegenerative disease resulting from a complex interplay between genetics and environment. Impairments in axonal transport have been identified in several ALS models, but in vivo evidence remains limited, thus their pathogenetic importance remains to be fully resolved. We therefore analyzed the in vivo dynamics of retrogradely transported, neurotrophin-containing signaling endosomes in nerve axons of two ALS mouse models with mutations in the RNA processing genes TARDBP and FUS. TDP-43M337V mice, which show neuromuscular pathology without motor neuron loss, display axonal transport perturbations manifesting between 1.5 and 3 months and preceding symptom onset. Contrastingly, despite 20% motor neuron loss, transport remained largely unaffected in FusΔ14/+ mice. Deficiencies in retrograde axonal transport of signaling endosomes are therefore not shared by all ALS-linked genes, indicating that there are mechanistic distinctions in the pathogenesis of ALS caused by mutations in different RNA processing genes. : Sleigh et al. address the importance of disturbances in axonal transport in two mouse models for ALS. They find that deficiencies in the in vivo axonal delivery of target tissue-derived survival factors are not a common feature of all ALS mouse models, suggesting mechanistic distinctions in different ALS-linked genes. Keywords: amyotrophic lateral sclerosis, ALS, intravital imaging, motor neuron disease, MND, RNA-binding protein, TARDBP
    Keywords Biology (General) ; QH301-705.5
    Language English
    Publishing date 2020-03-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis

    Daniel Jutzi / Sébastien Campagne / Ralf Schmidt / Stefan Reber / Jonas Mechtersheimer / Foivos Gypas / Christoph Schweingruber / Martino Colombo / Christine von Schroetter / Fionna E. Loughlin / Anny Devoy / Eva Hedlund / Mihaela Zavolan / Frédéric H.-T. Allain / Marc-David Ruepp

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 14

    Abstract: Mutations in the RNA binding protein FUS cause amyotrophic lateral sclerosis (ALS). Here the authors characterize FUS-binding to U1 snRNP and show that ALS-associated FUS aberrantly contacts U1 snRNA which interferes with its biogenesis pathway. ...

    Abstract Mutations in the RNA binding protein FUS cause amyotrophic lateral sclerosis (ALS). Here the authors characterize FUS-binding to U1 snRNP and show that ALS-associated FUS aberrantly contacts U1 snRNA which interferes with its biogenesis pathway.
    Keywords Science ; Q
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models

    Anny Devoy / Georgia Price / Francesca De Giorgio / Rosie Bunton-Stasyshyn / David Thompson / Samanta Gasco / Alasdair Allan / Gemma F. Codner / Remya R. Nair / Charlotte Tibbit / Ross McLeod / Zeinab Ali / Judith Noda / Alessandro Marrero-Gagliardi / José M. Brito-Armas / Muhammet M. Öztürk / Michelle Simon / Edward O’Neill / Sam Bryce-Smith /
    Jackie Harrison / Gemma Atkins / Silvia Corrochano / Michelle Stewart / Lydia Teboul / Abraham Acevedo-Arozena / Elizabeth M.C. Fisher / Thomas J. Cunningham

    iScience, Vol 25, Iss 4, Pp 103999- (2022)

    2022  

    Keywords Science ; Q
    Language English
    Publishing date 2022-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models

    Anny Devoy / Georgia Price / Francesca De Giorgio / Rosie Bunton-Stasyshyn / David Thompson / Samanta Gasco / Alasdair Allan / Gemma F. Codner / Remya R. Nair / Charlotte Tibbit / Ross McLeod / Zeinab Ali / Judith Noda / Alessandro Marrero-Gagliardi / José M. Brito-Armas / Muhammet M. Öztürk / Michelle Simon / Edward O'Neill / Sam Bryce-Smith /
    Jackie Harrison / Gemma Atkins / Silvia Corrochano / Michelle Stewart / Lydia Teboul / Abraham Acevedo-Arozena / Elizabeth M.C. Fisher / Thomas J. Cunningham

    iScience, Vol 24, Iss 12, Pp 103463- (2021)

    2021  

    Abstract: Summary: Amyotrophic lateral sclerosis/frontotemporal dementia (ALS/FTD) is a fatal neurodegenerative disorder, and continued innovation is needed for improved understanding and for developing therapeutics. We have created next-generation genomically ... ...

    Abstract Summary: Amyotrophic lateral sclerosis/frontotemporal dementia (ALS/FTD) is a fatal neurodegenerative disorder, and continued innovation is needed for improved understanding and for developing therapeutics. We have created next-generation genomically humanized knockin mouse models, by replacing the mouse genomic region of Sod1, Tardbp (TDP-43), and Fus, with their human orthologs, preserving human protein biochemistry and splicing with exons and introns intact. We establish a new standard of large knockin allele quality control, demonstrating the utility of indirect capture for enrichment of a genomic region of interest followed by Oxford Nanopore sequencing. Extensive analysis shows that homozygous humanized animals only express human protein at endogenous levels. Characterization of humanized FUS animals showed that they are phenotypically normal throughout their lifespan. These humanized strains are vital for preclinical assessment of interventions and serve as templates for the addition of coding or non-coding human ALS/FTD mutations to dissect disease pathomechanisms, in a physiological context.
    Keywords Neurogenetics ; Neuroscience ; Model organism ; Science ; Q
    Language English
    Publishing date 2021-12-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins

    Mizielinska, Sarah / Adrian M. Isaacs / Andrew J. Nicoll / Anny Devoy / Charlotte E. Ridler / Elizabeth M. C. Fisher / Emma L. Clayton / Frances E. Norona / Ione O. C. Woollacott / Jacqueline Dols / Julian Pietrzyk / Karen Cleverley / Linda Partridge / Melissa Cabecinha / Oliver Hendrich / Pietro Fratta / Sebastian Grönke / Stuart Pickering-Brown / Teresa Niccoli /
    Thomas Moens

    Science. 2014 Sept. 5, v. 345, no. 6201

    2014  

    Abstract: Dipeptide repeat peptides on the attack Certain neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), are associated with expanded dipeptides translated from RNA transcripts of disease-associated genes (see the Perspective by West ... ...

    Abstract Dipeptide repeat peptides on the attack Certain neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), are associated with expanded dipeptides translated from RNA transcripts of disease-associated genes (see the Perspective by West and Gitler). Kwon et al. show that the peptides encoded by the expanded repeats in the C9orf72 gene interfere with the way cells make RNA and kill cells. These effects may account for how this genetic form of ALS causes disease. Working in Drosophila , Mizielinska et al. aimed to distinguish between the effects of repeat-containing RNAs and the dipeptide repeat peptides that they encode. The findings provide evidence that dipeptide repeat proteins can cause toxicity directly. Science , this issue p. 1139 and p. 1192; see also p. 1118
    Keywords amyotrophic lateral sclerosis ; dipeptides ; Drosophila ; genes ; messenger RNA ; proteins ; toxicity ; translation (genetics)
    Language English
    Dates of publication 2014-0905
    Size p. 1192-1194.
    Publishing place American Association for the Advancement of Science
    Document type Article
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.1256800
    Database NAL-Catalogue (AGRICOLA)

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