Literature DB >> 11173222

Immunodetection of Parkin protein in vertebrate and invertebrate brains: a comparative study using specific antibodies.

J M Horowitz1, V A Vernace, J Myers, M K Stachowiak, D W Hanlon, G S Fraley, G Torres.   

Abstract

Parkin is an intracellular protein that plays a significant role in the etiopathogenesis of autosomal recessive juvenile parkinsonism. Using immunoblot methods, we found Parkin isoforms varying from 54 to 58 kDa in rat, mouse, bird, frog and fruit-fly brains. Immunocytochemical studies carried out in rats, mice and birds demonstrated multiple cell types bearing the phenotype for Parkin throughout telencephalic, diencephalic, mesencephalic and metencephalic brain structures. While in some instances Parkin-containing neurons tended to be grouped into clusters, the majority of these labeled nerve cells were widely scattered throughout the neuraxis. The topographical distribution and organizational pattern of Parkin within major functional brain circuits was comparable in both rats and mice. However, the subcellular localization of Parkin was found to vary significantly as a function of antibody reactivity. A consistent cytoplasmic labeling for Parkin was observed in rodent tissue incubated with a polyclonal antibody raised against the human Parkin protein and having an identical amino-acid sequence with that of the rat. In contrast, rodent tissue alternately incubated with a polyclonal antibody raised against a different region of the same human Parkin protein but having 10 mismatched amino-acid sequence changes with those of the rat and mouse, resulted in nuclear labeling for Parkin in rat but not mouse neurons. This difference in epitope recognition, however, was reversed when mouse brain tissue was heated at 80 degrees C, apparently unmasking target epitopes against which the antisera were directed. Collectively, these results show a high degree of conservation in the cellular identity of Parkin in animals as different as drosophilids and mammals and points to the possibility that the biochemical specificities of Parkin, including analogous functional roles, may have been conserved during the course of evolution.

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Year:  2001        PMID: 11173222     DOI: 10.1016/s0891-0618(00)00111-3

Source DB:  PubMed          Journal:  J Chem Neuroanat        ISSN: 0891-0618            Impact factor:   3.052


  11 in total

1.  Parkin transcript variants in rat and human brain.

Authors:  Velia Dagata; Sebastiano Cavallaro
Journal:  Neurochem Res       Date:  2004-09       Impact factor: 3.996

2.  Alarin stimulates food intake in male rats and LH secretion in castrated male rats.

Authors:  Nicole Van Der Kolk; Farrah N Madison; Margaret Mohr; Nicole Eberhard; Barbara Kofler; Gregory S Fraley
Journal:  Neuropeptides       Date:  2010-08       Impact factor: 3.286

3.  Proteomic Analysis of Parkin Isoforms Expression in Different Rat Brain Areas.

Authors:  Agata Grazia D'Amico; Grazia Maugeri; Rita Reitano; Sebastiano Cavallaro; Velia D'Agata
Journal:  Protein J       Date:  2016-10       Impact factor: 2.371

4.  Inhibition of proteasomal activity causes inclusion formation in neuronal and non-neuronal cells overexpressing Parkin.

Authors:  Helen C Ardley; Gina B Scott; Stephen A Rose; Nancy G S Tan; Alexander F Markham; Philip A Robinson
Journal:  Mol Biol Cell       Date:  2003-08-22       Impact factor: 4.138

5.  Parkin expression profile in dopamine d3 receptor knock-out mice brains.

Authors:  Velia D'Agata; Adriana Tiralongo; Alessandro Castorina; Gian Marco Leggio; Vincenzo Micale; Maria Luisa Carnazza; Filippo Drago
Journal:  Neurochem Res       Date:  2008-07-09       Impact factor: 3.996

Review 6.  Modelling Parkinson's disease in Drosophila.

Authors:  José A Botella; Florian Bayersdorfer; Florian Gmeiner; Stephan Schneuwly
Journal:  Neuromolecular Med       Date:  2009-10-24       Impact factor: 3.843

7.  Neurons that co-localize aromatase- and kisspeptin-like immunoreactivity may regulate the HPG axis of the Mallard drake (Anas platyrhynchos).

Authors:  Colin J Saldanha; Bradley J Walters; Gregory S Fraley
Journal:  Gen Comp Endocrinol       Date:  2010-01-11       Impact factor: 2.822

Review 8.  Parkin's substrates and the pathways leading to neuronal damage.

Authors:  Mark R Cookson
Journal:  Neuromolecular Med       Date:  2003       Impact factor: 4.103

9.  Increasing the Coding Potential of Genomes Through Alternative Splicing: The Case of PARK2 Gene.

Authors:  Valentina La Cognata; Rosario Iemmolo; Velia D'Agata; Soraya Scuderi; Filippo Drago; Mario Zappia; Sebastiano Cavallaro
Journal:  Curr Genomics       Date:  2014-06       Impact factor: 2.236

10.  Alternative splicing generates different parkin protein isoforms: evidences in human, rat, and mouse brain.

Authors:  Soraya Scuderi; Valentina La Cognata; Filippo Drago; Sebastiano Cavallaro; Velia D'Agata
Journal:  Biomed Res Int       Date:  2014-07-16       Impact factor: 3.411

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