Literature DB >> 12547513

An evolutionary basis for scrapie disease: identification of a fish prion mRNA.

Eric Rivera-Milla1, Claudia A O Stuermer, Edward Málaga-Trillo.   

Abstract

Infectious prion proteins cause neurodegenerative disease in mammals owing to the acquisition of an aberrant conformation. We cloned a Fugu rubripes gene that encodes a structurally conserved prion protein, and found rapid rates of molecular divergence among prions from different vertebrate classes, along with molecular stasis within each class. We propose that a directional trend in the evolution of prion sequence motifs associated with pathogenesis and infectivity could account for the origin of scrapie in mammals.

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Year:  2003        PMID: 12547513     DOI: 10.1016/s0168-9525(02)00032-x

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  12 in total

1.  The mechanism of internalization of glycosylphosphatidylinositol-anchored prion protein.

Authors:  Claire Sunyach; Angela Jen; Juelin Deng; Kathleen T Fitzgerald; Yveline Frobert; Jacques Grassi; Mary W McCaffrey; Roger Morris
Journal:  EMBO J       Date:  2003-07-15       Impact factor: 11.598

Review 2.  PrPs: Proteins with a purpose: Lessons from the zebrafish.

Authors:  Edward Málaga-Trillo; Emily Sempou
Journal:  Prion       Date:  2009-07-29       Impact factor: 3.931

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

Authors:  Tuğçe Birkan; Mesut Şahin; Zubeyde Öztel; Erdal Balcan
Journal:  J Biosci       Date:  2016-03       Impact factor: 1.826

4.  Cloning of the bovine prion-like Shadoo (SPRN) gene by comparative analysis of the predicted genomic locus.

Authors:  Cristina Uboldi; Marianna Paulis; Elena Guidi; Anna Bertoni; Giulia Pia Di Meo; Angela Perucatti; Leopoldo Iannuzzi; Elena Raimondi; Ronald M Brunner; André Eggen; Luca Ferretti
Journal:  Mamm Genome       Date:  2006-11-07       Impact factor: 2.957

5.  Disruption of Doppel prevents neurodegeneration in mice with extensive Prnp deletions.

Authors:  Nicolas Genoud; Axel Behrens; Gino Miele; Dimitri Robay; Frank L Heppner; Stefan Freigang; Adriano Aguzzi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-08       Impact factor: 11.205

6.  Expression of cellular prion protein (PrP(c)) in schizophrenia, bipolar disorder, and depression.

Authors:  Serge Weis; Johannes Haybaeck; Jeannette R Dulay; Ida C Llenos
Journal:  J Neural Transm (Vienna)       Date:  2008-01-11       Impact factor: 3.575

7.  Evidence for retrogene origins of the prion gene family.

Authors:  Sepehr Ehsani; Renzhu Tao; Cosmin L Pocanschi; Hezhen Ren; Paul M Harrison; Gerold Schmitt-Ulms
Journal:  PLoS One       Date:  2011-10-27       Impact factor: 3.240

8.  Evolutionary descent of prion genes from the ZIP family of metal ion transporters.

Authors:  Gerold Schmitt-Ulms; Sepehr Ehsani; Joel C Watts; David Westaway; Holger Wille
Journal:  PLoS One       Date:  2009-09-28       Impact factor: 3.240

9.  Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata).

Authors:  Evgenia Salta; Cynthia Panagiotidis; Konstantinos Teliousis; Spyros Petrakis; Eleftherios Eleftheriadis; Fotis Arapoglou; Nikolaos Grigoriadis; Anna Nicolaou; Eleni Kaldrymidou; Grigorios Krey; Theodoros Sklaviadis
Journal:  PLoS One       Date:  2009-07-28       Impact factor: 3.240

10.  PrionHome: a database of prions and other sequences relevant to prion phenomena.

Authors:  Djamel Harbi; Marimuthu Parthiban; Deena M A Gendoo; Sepehr Ehsani; Manish Kumar; Gerold Schmitt-Ulms; Ramanathan Sowdhamini; Paul M Harrison
Journal:  PLoS One       Date:  2012-02-20       Impact factor: 3.240

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