The human "prion-like" protein Doppel is expressed in both Sertoli cells and spermatozoa (Q28219319)

GOA release 2020-03-11

9

Pierre Jouannet

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Katell Peoc'h

object named as

Katell Peoc'h

1

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Sylvain Lehmann

object named as

Sylvain Lehmann

5

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author name string

Catherine Serres

2

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Yveline Frobert

3

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Caroline Martin

4

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Stephanie Chasseigneaux

6

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Veronique Sazdovitch

7

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Jacques Grassi

8

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Jean-Marie Launay

10

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Jean-Louis Laplanche

Journal of Biological Chemistry

11

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language of work or name

English

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publication date

8 November 2002

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published in

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volume

277

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issue

45

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page(s)

43071-8

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cites work

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Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

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Doppel-induced cerebellar degeneration in transgenic mice

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Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

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The cellular prion protein binds copper in vivo

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Prion infection impairs the cellular response to oxidative stress

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Prions prevent neuronal cell-line death.

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Signal transduction through prion protein

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Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel

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Nearly ubiquitous tissue distribution of the scrapie agent precursor protein

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The PrP-like protein Doppel gene in sheep and cattle: cDNA sequence and expression

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Two different neurodegenerative diseases caused by proteins with similar structures

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Expression and structural characterization of the recombinant human doppel protein

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First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

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Truncated forms of the human prion protein in normal brain and in prion diseases

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Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

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A new method for predicting signal sequence cleavage sites

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Physiological expression of the gene for PrP-like protein, PrPLP/Dpl, by brain endothelial cells and its ectopic expression in neurons of PrP-deficient mice ataxic due to Purkinje cell degeneration

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Doppel is an N-glycosylated, glycosylphosphatidylinositol-anchored protein. Expression in testis and ectopic production in the brains of Prnp(0/0) mice predisposed to Purkinje cell loss

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Absence of the prion protein homologue Doppel causes male sterility

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Cell-to-cell transfer of glycosylphosphatidylinositol-anchored membrane proteins during sperm maturation

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Functional processing of fertilin: evidence for a critical role of proteolysis in sperm maturation and activation

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Metal ions and prion diseases

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Expression of doppel in the CNS of mice does not modulate transmissible spongiform encephalopathy disease

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Glycosyl Phosphatidylinositol-Anchored Ceruloplasmin Is Expressed by Rat Sertoli Cells and Is Concentrated in Detergent-Insoluble Membrane Fractions1

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A C-terminal-truncated PrP Isoform Is Present in Mature Sperm

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Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene

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B lymphocytes and neuroinvasion

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Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

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New insight into abnormal prion protein using monoclonal antibodies

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Male-specific modification of human CD52

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