Literature DB >> 8408300

Expression of high molecular weight tau in the central and peripheral nervous systems.

I S Georgieff1, R K Liem, D Couchie, C Mavilia, J Nunez, M L Shelanski.   

Abstract

Using a novel PCR approach, we have cloned a cDNA encoding the entire high molecular weight tau molecule from rat dorsal root ganglia. The resulting 2080 bp cDNA differs from low molecular weight rat brain tau by the insertion of a novel 762 bp region (exon 4a) between exons 4 and 5. This cDNA clone is identical in sequence with a high molecular weight tau (HMW) cDNA from rat PC12 tumor cells and is closely related to a HMW tau cDNA from mouse N115 tumor cells. In vitro transcription/translation produces a protein that migrates on SDS-PAGE with the same apparent molecular weight as HMW tau purified from rat sciatic nerve. The HMW tau protein is generated from an 8 kb mRNA, which can be detected by northern blots in peripheral ganglia, but not in brain. A more sensitive assay using PCR and Southern blot analysis demonstrates the presence of exon 4a in spinal cord and in retina. In combination with immunohistochemical studies of spinal cord, these data suggest that HMW tau, though primarily in the peripheral nervous system, is also expressed in limited areas of the central nervous system, although its presence cannot be detected in the cerebral cortices.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8408300     DOI: 10.1242/jcs.105.3.729

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  18 in total

Review 1.  The elimination of accumulated and aggregated proteins: a role for aggrephagy in neurodegeneration.

Authors:  Ai Yamamoto; Anne Simonsen
Journal:  Neurobiol Dis       Date:  2010-08-20       Impact factor: 5.996

2.  Impairments in fast axonal transport and motor neuron deficits in transgenic mice expressing familial Alzheimer's disease-linked mutant presenilin 1.

Authors:  Orly Lazarov; Gerardo A Morfini; Gustavo Pigino; Archana Gadadhar; Xiangjun Chen; John Robinson; Hanson Ho; Scott T Brady; Sangram S Sisodia
Journal:  J Neurosci       Date:  2007-06-27       Impact factor: 6.167

Review 3.  Microtubule-associated proteins (MAPs) in the peripheral nervous system during development and regeneration.

Authors:  J Nunez; I Fischer
Journal:  J Mol Neurosci       Date:  1997-06       Impact factor: 3.444

4.  Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis.

Authors:  Ewa Usarek; Magdalena Kuźma-Kozakiewicz; Birgit Schwalenstöcker; Beata Kaźmierczak; Christoph Münch; Albert C Ludolph; Anna Barańczyk-Kuźma
Journal:  Neurochem Res       Date:  2006-05-23       Impact factor: 3.996

5.  High molecular weight tau distribution and microtubule stability in neuroblastoma N115 cells.

Authors:  Y Gache; J Guilleminot; J Nunez
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

6.  Age-related changes in tau expression in transgenic mouse model of amyotrophic lateral sclerosis.

Authors:  Anna Barańczyk-Kuźma; Ewa Usarek; Magdalena Kuźma-Kozakiewcz; Beata Kaźmierczak; Beata Gajewska; Birgit Schwalenstocker; Albert C Ludolph
Journal:  Neurochem Res       Date:  2007-03       Impact factor: 3.996

Review 7.  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

8.  Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disorders.

Authors:  U Lübke; J Six; M Villanova; J Boons; M Vandermeeren; C Ceuterick; P Cras; J J Martin
Journal:  Am J Pathol       Date:  1994-07       Impact factor: 4.307

Review 9.  The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

Authors:  Vladimir N Uversky
Journal:  Autophagy       Date:  2017-12-17       Impact factor: 16.016

10.  Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron disease.

Authors:  Magdalena Kuźma-Kozakiewicz; Ewa Usarek; Albert C Ludolph; Anna Barańczyk-Kuźma
Journal:  Neurochem Res       Date:  2011-03-06       Impact factor: 3.996

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.