Literature DB >> 15615649

Tau and src family tyrosine kinases.

Gloria Lee1.   

Abstract

The interaction between tau and src family non-receptor tyrosine kinases represents a new function for tau. Mediated by the proline-rich region of tau and the SH3 domain of fyn or src, this interaction has the potential to confer novel cellular activities for tau in the growth cone and in the membrane. The subsequent finding that tau is tyrosine phosphorylated has led to the observation that tau in neurofibrillary tangles is tyrosine phosphorylated. Therefore, a role for tyrosine kinases such as fyn in neuropathogenesis is predicted.

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Year:  2005        PMID: 15615649     DOI: 10.1016/j.bbadis.2004.09.002

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  40 in total

1.  Tau is endogenously nitrated in mouse brain: identification of a tyrosine residue modified in vivo by NO.

Authors:  Simona Nonnis; Graziella Cappelletti; Francesca Taverna; Cristina Ronchi; Severino Ronchi; Armando Negri; Eleonora Grassi; Gabriella Tedeschi
Journal:  Neurochem Res       Date:  2007-09-02       Impact factor: 3.996

2.  The amino terminus of tau inhibits kinesin-dependent axonal transport: implications for filament toxicity.

Authors:  Nichole E LaPointe; Gerardo Morfini; Gustavo Pigino; Irina N Gaisina; Alan P Kozikowski; Lester I Binder; Scott T Brady
Journal:  J Neurosci Res       Date:  2009-02       Impact factor: 4.164

3.  Tuning microtubule-based transport through filamentous MAPs: the problem of dynein.

Authors:  Michael Vershinin; Jing Xu; David S Razafsky; Stephen J King; Steven P Gross
Journal:  Traffic       Date:  2008-03-28       Impact factor: 6.215

Review 4.  Tau splicing and the intricacies of dementia.

Authors:  Athena Andreadis
Journal:  J Cell Physiol       Date:  2012-03       Impact factor: 6.384

5.  Differential changes in phosphorylation of tau at PHF-1 and 12E8 epitopes during brain ischemia and reperfusion in gerbils.

Authors:  W Gordon-Krajcer; E Kozniewska; J W Lazarewicz; H Ksiezak-Reding
Journal:  Neurochem Res       Date:  2006-12-27       Impact factor: 3.996

Review 6.  It's all about tau.

Authors:  Cheril Tapia-Rojas; Fabian Cabezas-Opazo; Carol A Deaton; Erick H Vergara; Gail V W Johnson; Rodrigo A Quintanilla
Journal:  Prog Neurobiol       Date:  2018-12-31       Impact factor: 11.685

Review 7.  Emerging role for SRC family kinases in junction dynamics during spermatogenesis.

Authors:  Xiang Xiao; Yue Yang; Baiping Mao; C Yan Cheng; Ya Ni
Journal:  Reproduction       Date:  2019-03       Impact factor: 3.906

Review 8.  Brain hypometabolism triggers PHF-like phosphorylation of tau, a major hallmark of Alzheimer's disease pathology.

Authors:  Thomas Arendt; Jens Stieler; Max Holzer
Journal:  J Neural Transm (Vienna)       Date:  2014-12-06       Impact factor: 3.575

9.  Small proline-rich proteins (SPRR) function as SH3 domain ligands, increase resistance to injury and are associated with epithelial-mesenchymal transition (EMT) in cholangiocytes.

Authors:  Anthony J Demetris; Susan Specht; Isao Nozaki; John G Lunz; Donna Beer Stolz; Noriko Murase; Tong Wu
Journal:  J Hepatol       Date:  2007-12-17       Impact factor: 25.083

10.  The proline-rich domain of tau plays a role in interactions with actin.

Authors:  Hai Jin He; Xing Sheng Wang; Rong Pan; Dong Liang Wang; Ming Nan Liu; Rong Qiao He
Journal:  BMC Cell Biol       Date:  2009-11-08       Impact factor: 4.241

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