Promiscuous functions of the prion protein gene family

The cellular prion protein PrPC is a ubiquitous GPI-anchored protein. While PrPC has been the focus of intense research for its involvement in a group of neurodegenerative disorders known as transmissible spongiform encephalopathies (TSE), much less attention has been devoted to its physiological fu...

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Հիմնական հեղինակներ: Jean-Luc Vilotte, Sophie Mouillet-Richard
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Հրապարակվել է: Frontiers Media SA 2021
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Առցանց հասանելիություն:19513
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author Jean-Luc Vilotte
Sophie Mouillet-Richard
author_browse Jean-Luc Vilotte
Sophie Mouillet-Richard
author_facet Jean-Luc Vilotte
Sophie Mouillet-Richard
author_sort Jean-Luc Vilotte
collection Directory of Open Access Books
description The cellular prion protein PrPC is a ubiquitous GPI-anchored protein. While PrPC has been the focus of intense research for its involvement in a group of neurodegenerative disorders known as transmissible spongiform encephalopathies (TSE), much less attention has been devoted to its physiological function. This notably relates to the lack of obvious abnormalities of mice, goat or cattle lacking PrPC. This apparently normal phenotype in these PrPC-deficient animals however contrasts with the very high degree of conservation of the prion protein gene (Prnp) in mammalian species (over 80%), and the presence of genes with similarities to Prnp in birds, reptiles, amphibians and fish. This high conservation together with its ubiquitous expression, - albeit at highest levels in the brain-, suggest that PrPC has major physiological functions. Dissecting PrPC function is further complicated by the occurrence, in mammals, of two potentially partially redundant homologues, Doppel, and Shadoo. The biological overlaps between members of the prion protein family are still under investigation and much debated. Similarly, although in vitro analyses have suggested various functions for PrPC, notably in cell death and survival processes, some have yielded conflicting results and/or discrepancies with in vivo studies. This Research Topic brings together the accumulated knowledge regarding the biological roles of the prion protein family, from the animal to the molecular scale.
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spelling doab-20.500.12854ir-571812024-04-05T12:32:40Z Promiscuous functions of the prion protein gene family Jean-Luc Vilotte Sophie Mouillet-Richard QH301-705.5 Q1-390 Stem Cells Neuroprotection Placenta abeta Aging Embryonic and Fetal Development Cell Adhesion Gonads Cell signaling prion protein thema EDItEUR::P Mathematics and Science::PS Biology, life sciences The cellular prion protein PrPC is a ubiquitous GPI-anchored protein. While PrPC has been the focus of intense research for its involvement in a group of neurodegenerative disorders known as transmissible spongiform encephalopathies (TSE), much less attention has been devoted to its physiological function. This notably relates to the lack of obvious abnormalities of mice, goat or cattle lacking PrPC. This apparently normal phenotype in these PrPC-deficient animals however contrasts with the very high degree of conservation of the prion protein gene (Prnp) in mammalian species (over 80%), and the presence of genes with similarities to Prnp in birds, reptiles, amphibians and fish. This high conservation together with its ubiquitous expression, - albeit at highest levels in the brain-, suggest that PrPC has major physiological functions. Dissecting PrPC function is further complicated by the occurrence, in mammals, of two potentially partially redundant homologues, Doppel, and Shadoo. The biological overlaps between members of the prion protein family are still under investigation and much debated. Similarly, although in vitro analyses have suggested various functions for PrPC, notably in cell death and survival processes, some have yielded conflicting results and/or discrepancies with in vivo studies. This Research Topic brings together the accumulated knowledge regarding the biological roles of the prion protein family, from the animal to the molecular scale. 2021-02-12T00:10:45Z 2021-02-12T00:10:45Z 2016-08-16 10:34:25 2015 book 19513 16648714 9782889196050 https://directory.doabooks.org/handle/20.500.12854/57181 eng Frontiers Research Topics image/jpeg Attribution 4.0 International http://www.frontiersin.org/books/Promiscuous_Functions_of_the_Prion_Protein_Gene_Family/645#nogo http://journal.frontiersin.org/researchtopic/2567/promiscuous-functions-of-the-prion-protein-gene-family Frontiers Media SA 10.3389/978-2-88919-605-0 10.3389/978-2-88919-605-0 bf5ce210-e72e-4860-ba9b-c305640ff3ae 9782889196050 113 open access
spellingShingle QH301-705.5
Q1-390
Stem Cells
Neuroprotection
Placenta
abeta
Aging
Embryonic and Fetal Development
Cell Adhesion
Gonads
Cell signaling
prion protein
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
Jean-Luc Vilotte
Sophie Mouillet-Richard
Promiscuous functions of the prion protein gene family
title Promiscuous functions of the prion protein gene family
title_full Promiscuous functions of the prion protein gene family
title_fullStr Promiscuous functions of the prion protein gene family
title_full_unstemmed Promiscuous functions of the prion protein gene family
title_short Promiscuous functions of the prion protein gene family
title_sort promiscuous functions of the prion protein gene family
topic QH301-705.5
Q1-390
Stem Cells
Neuroprotection
Placenta
abeta
Aging
Embryonic and Fetal Development
Cell Adhesion
Gonads
Cell signaling
prion protein
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
topic_facet QH301-705.5
Q1-390
Stem Cells
Neuroprotection
Placenta
abeta
Aging
Embryonic and Fetal Development
Cell Adhesion
Gonads
Cell signaling
prion protein
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
url 19513
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AT sophiemouilletrichard promiscuousfunctionsoftheprionproteingenefamily