Literature DB >> 12965213

The AXH module: an independently folded domain common to ataxin-1 and HBP1.

C de Chiara1, C Giannini, S Adinolfi, J de Boer, S Guida, A Ramos, C Jodice, D Kioussis, A Pastore.   

Abstract

Ataxin-1 (ATX1), a human protein responsible for spinocerebellar ataxia type 1 in humans, shares a region of homology, named AXH module, with the apparently unrelated transcription factor HBP1. Here, we describe the first characterisation of the AXH module in terms of its structural properties and stability. By producing protein constructs spanning the AXH modules of ATX1 and HBP1 and by comparing their properties, we have identified the minimal region sufficient for forming independently folded units (domains). Knowledge of the AXH domain boundaries allows us to map many of the interactions of ATX1 with other molecules onto the AXH module. We further show that the AXH of ATX1 is a dimerisation domain and is able to recognise RNA with the same nucleotide preference previously described for the full-length protein. AXH is therefore a novel protein-protein and RNA binding motif.

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Year:  2003        PMID: 12965213     DOI: 10.1016/s0014-5793(03)00818-4

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  28 in total

Review 1.  Nuclear ataxias.

Authors:  Harry T Orr
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-05       Impact factor: 10.005

2.  Evolution and conservation of JmjC domain proteins in the green lineage.

Authors:  Yong Huang; Donghong Chen; Chunlin Liu; Wenhui Shen; Ying Ruan
Journal:  Mol Genet Genomics       Date:  2015-07-08       Impact factor: 3.291

3.  Destabilizing the AXH Tetramer by Mutations: Mechanisms and Potential Antiaggregation Strategies.

Authors:  Gianvito Grasso; Umberto Morbiducci; Diana Massai; Jack A Tuszynski; Andrea Danani; Marco A Deriu
Journal:  Biophys J       Date:  2018-01-23       Impact factor: 4.033

4.  The HBP1 transcriptional repressor participates in RAS-induced premature senescence.

Authors:  Xiaowei Zhang; Jiyoung Kim; Robin Ruthazer; Michael A McDevitt; David E Wazer; K Eric Paulson; Amy S Yee
Journal:  Mol Cell Biol       Date:  2006-09-11       Impact factor: 4.272

Review 5.  Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1.

Authors:  Huda Y Zoghbi; Harry T Orr
Journal:  J Biol Chem       Date:  2008-10-28       Impact factor: 5.157

6.  RNAi or overexpression: alternative therapies for Spinocerebellar Ataxia Type 1.

Authors:  Megan S Keiser; James C Geoghegan; Ryan L Boudreau; Kim A Lennox; Beverly L Davidson
Journal:  Neurobiol Dis       Date:  2013-04-10       Impact factor: 5.996

Review 7.  Polyglutamine spinocerebellar ataxias - from genes to potential treatments.

Authors:  Henry L Paulson; Vikram G Shakkottai; H Brent Clark; Harry T Orr
Journal:  Nat Rev Neurosci       Date:  2017-08-17       Impact factor: 34.870

8.  Characterization of the zebrafish atxn1/axh gene family.

Authors:  Kerri M Carlson; Laura Melcher; Shaojuan Lai; Huda Y Zoghbi; H Brent Clark; Harry T Orr
Journal:  J Neurogenet       Date:  2008-12-10       Impact factor: 1.250

9.  Assignment of the 1H, 13C, and 15N resonances of the AXH domain of the transcription factor HBP1.

Authors:  Cesira de Chiara; Geoff Kelly; Thomas A Frenkiel; Annalisa Pastore
Journal:  J Biomol NMR       Date:  2004-04       Impact factor: 2.835

10.  Phosphorylation of S776 and 14-3-3 binding modulate ataxin-1 interaction with splicing factors.

Authors:  Cesira de Chiara; Rajesh P Menon; Molly Strom; Toby J Gibson; Annalisa Pastore
Journal:  PLoS One       Date:  2009-12-23       Impact factor: 3.240

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