کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8478449 | 1551130 | 2016 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
ALS-FTLD associated mutations of SQSTM1 impact on Keap1-Nrf2 signalling
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کلمات کلیدی
FTLDNQO1mTORC1NFE2L2inhibitor of nuclear factor kappa-B kinase subunit betaSALSTDP-43SOD1KirIKKβUBANrf2PDBNuclear factor erythroid 2-like 2NAD(P)H dehydrogenase, quinone 1sporadic ALS - ALS پراکندهkeap1 - buy1SQSTM1/p62 - SQSTM1 / p62amyotrophic lateral sclerosis - اسکلروز جانبی آمیوتروفیکLIR - بهALS - بیماری اسکلروز جانبی آمیوتروفیکPaget's disease of bone - بیماری پگت استخوانOxidative stress - تنش اکسیداتیوfrontotemporal lobar degeneration - دژنراسیون لوبار قبل از مواجههsuperoxide dismutase 1 - سوپر اکسید دیسموتاز 1nuclear erythroid 2-related factor 2 - عامل اریتروتیک هسته ای 2 عامل 2antioxidant response element - عنصر پاسخ آنتی اکسیدانLC3-interacting region - منطقه LC3 تعاملMammalian target of rapamycin complex 1 - هدف پستانداران مجتمع رپامایسین 1ARE - هستندtar DNA-binding protein 43 - پروتئین متصل به DNA DNA 39Kelch-like ECH-associated protein 1 - پروتئین مرتبط با ECH کلچ 1
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
بیولوژی سلول
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
The transcription factor Nrf2 and its repressor protein Keap1 play key roles in the regulation of antioxidant stress responses and both Keap1-Nrf2 signalling and oxidative stress have been implicated in the pathogenesis of the ALS-FTLD spectrum of neurodegenerative disorders. The Keap1-binding partner and autophagy receptor SQSTM1/p62 has also recently been linked genetically to ALS-FTLD, with some missense mutations identified in patients mapping within or close to its Keap1-interacting region (KIR, residues 347-352). Here we report the effects on protein function of four different disease associated mutations of SQSTM1/p62 which affect the KIR region. Only mutations mapping precisely to the KIR (P348L and G351A) were associated with a loss of Keap1 binding in co-immunoprecipitations comparable to wild-type SQSTM1/p62. These selective effects on Keap1 recognition were entirely rational based on protein structural models. Consistent with impaired Keap1 binding, the P348L and G351A KIR mutants showed reduced ability to activate Nrf2 signalling compared to wild-type SQSTM1/p62 in antioxidant response element (ARE)-luciferase reporter assays. The results suggest that SQSTM1 mutations within the KIR of SQSTM1/p62 contribute to aetiology of some cases of ALS-FTLD through a mechanism involving aberrant expression or regulation of oxidative response genes.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular and Cellular Neuroscience - Volume 76, October 2016, Pages 52-58
Journal: Molecular and Cellular Neuroscience - Volume 76, October 2016, Pages 52-58
نویسندگان
Alice Goode, Sarah Rea, Melanie Sultana, Barry Shaw, Mark S. Searle, Robert Layfield,