Literature DB >> 26949092

Do prion protein gene polymorphisms induce apoptosis in non-mammals?

Tuğçe Birkan1, Mesut Şahin, Zubeyde Öztel, Erdal Balcan.   

Abstract

Genetic variations such as single nucleotide polymorphisms (SNPs) in prion protein coding gene, Prnp, greatly affect susceptibility to prion diseases in mammals. Here, the coding region of Prnp was screened for polymorphisms in redeared turtle, Trachemys scripta. Four polymorphisms, L203V, N205I, V225A and M237V, were common in 15 out of 30 turtles; in one sample, three SNPs, L203V, N205I and M237V, and in the remaining 14 samples, only L203V and N205I polymorphisms, were investigated. Besides, C658T, C664T, C670A and C823A SNPs were silent mutations. To elucidate the relationship between the SNPs and apoptosis, TUNEL assays and active caspase-3 immunodetection techniques in brain sections of the polymorphic samples were performed. The results revealed that TUNEL-positive cells and active caspase-3-positive cells in the turtles with four polymorphisms were significantly increased compared with those of the turtles with two polymorphisms (P less than 0.01 and P less than 0.05, respectively). In conclusion, this study provides preliminary information about the possible relationship between SNPs within the Prnp locus and apoptosis in a non-mammalian species, Trachemys scripta, in which prion disease has never been reported.

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Year:  2016        PMID: 26949092     DOI: 10.1007/s12038-015-9584-7

Source DB:  PubMed          Journal:  J Biosci        ISSN: 0250-5991            Impact factor:   1.826


  87 in total

1.  Cellular and subcellular morphological localization of normal prion protein in rodent cerebellum.

Authors:  J Lainé; M E Marc; M S Sy; H Axelrad
Journal:  Eur J Neurosci       Date:  2001-07       Impact factor: 3.386

2.  Effect of rapamycin on the fate of P23H opsin associated with retinitis pigmentosa (an American Ophthalmological Society thesis).

Authors:  Shalesh Kaushal
Journal:  Trans Am Ophthalmol Soc       Date:  2006

3.  Apoptosis in relation to neuronal loss in experimental Creutzfeldt-Jakob disease in mice.

Authors:  D Jesionek-Kupnicka; R Kordek; J Buczyński; P P Liberski
Journal:  Acta Neurobiol Exp (Wars)       Date:  2001       Impact factor: 1.579

4.  Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease.

Authors:  M S Palmer; A J Dryden; J T Hughes; J Collinge
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

5.  Overexpression of PrPc triggers caspase 3 activation: potentiation by proteasome inhibitors and blockade by anti-PrP antibodies.

Authors:  E Paitel; C Alves da Costa; D Vilette; J Grassi; F Checler
Journal:  J Neurochem       Date:  2002-12       Impact factor: 5.372

6.  Autophagy induced by resveratrol prevents human prion protein-mediated neurotoxicity.

Authors:  Jae-Kyo Jeong; Myung-Hee Moon; Bum-Chul Bae; You-Jin Lee; Jae-Won Seol; Hyung-Sub Kang; Jin-Shang Kim; Seog-Jin Kang; Sang-Youel Park
Journal:  Neurosci Res       Date:  2012-03-23       Impact factor: 3.304

7.  Disparate evolution of prion protein domains and the distinct origin of Doppel- and prion-related loci revealed by fish-to-mammal comparisons.

Authors:  Eric Rivera-Milla; Birgit Oidtmann; Cynthia H Panagiotidis; Michael Baier; Theodoros Sklaviadis; Rudolf Hoffmann; Yi Zhou; Gonzalo P Solis; Claudia A O Stuermer; Edward Málaga-Trillo
Journal:  FASEB J       Date:  2005-12-13       Impact factor: 5.191

Review 8.  Role of autophagy in prion protein-induced neurodegenerative diseases.

Authors:  Hao Yao; Deming Zhao; Sher Hayat Khan; Lifeng Yang
Journal:  Acta Biochim Biophys Sin (Shanghai)       Date:  2013-03-03       Impact factor: 3.848

9.  A novel protective prion protein variant that colocalizes with kuru exposure.

Authors:  Simon Mead; Jerome Whitfield; Mark Poulter; Paresh Shah; James Uphill; Tracy Campbell; Huda Al-Dujaily; Holger Hummerich; Jon Beck; Charles A Mein; Claudio Verzilli; John Whittaker; Michael P Alpers; John Collinge
Journal:  N Engl J Med       Date:  2009-11-19       Impact factor: 91.245

Review 10.  Protein misfolding and neurodegeneration.

Authors:  Claudio Soto; Lisbell D Estrada
Journal:  Arch Neurol       Date:  2008-02
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