Aminata Touré

Dr. Aminata Touré

Institute for Advanced Biosciences, Grenoble, Auvergne-Rhône-Alpes, France
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Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2014 in The American Journal of Human Genetics
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Journal Article
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MKMariem Ben Khelifa
Mariem Ben Khelifa
CCCharles Coutton
Charles Coutton
RZRaoudha Zouari
Raoudha Zouari
TKThomas Karaouzène
Thomas Karaouzène
JRJohn Rendu
John Rendu
PRPierre F. Ray
Pierre F. Ray

15 February 2018 in Nature Communications
Verified
Journal Article
Open access
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CCCharles Coutton
Charles Coutton
AVAlexandra S. Vargas
Alexandra S. Vargas
AAAmir Amiri-Yekta
Amir Amiri-Yekta
Zine-Eddine KherrafZine-Eddine Kherraf
Zine-Eddine Kherraf
SMSelima Fourati Ben Mustapha
Selima Fourati Ben Mustapha
PRPierre F. Ray
Pierre F. Ray
Spermatogenesis defects concern millions of men worldwide, yet the vast majority remains undiagnosed. Here we report men with primary infertility due to multiple morphological abnormalities of the sperm flagella with severe disorganization of the sperm axoneme, a microtubule-based structure highly conserved throughout evolution. Whole-exome sequencing was performed on 78 patients allowing the identification of 22 men with bi-allelic mutations in DNAH1 (n = 6), CFAP43 (n = 10), and CFAP44 (n = 6). CRISPR/Cas9 created homozygous CFAP43/44 male mice that were infertile and presented severe flagellar defects confirming the human genetic results. Immunoelectron and stimulated-emission-depletion microscopy performed on CFAP43 and CFAP44 orthologs in Trypanosoma brucei evidenced that both proteins are located between the doublet microtubules 5 and 6 and the paraflagellar rod. Overall, we demonstrate that CFAP43 and CFAP44 have a similar structure with a unique axonemal localization and are necessary to produce functional flagella in species ranging from Trypanosoma to human.

16 January 2020 in Human Genetics
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Aminata TouréAminata Touré
Aminata Touré
GMGuillaume Martinez
Guillaume Martinez
ZKZine-Eddine Kherraf
Zine-Eddine Kherraf
CCCaroline Cazin
Caroline Cazin
JBJulie Beurois
Julie Beurois
CCCharles Coutton
Charles Coutton

1 July 2019 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
MWMarjorie Whitfield
Marjorie Whitfield
LTLucie Thomas
Lucie Thomas
EBEmilie Bequignon
Emilie Bequignon
ASAlain Schmitt
Alain Schmitt
LSLaurence Stouvenel
Laurence Stouvenel
MLMarie Legendre
Marie Legendre

1 November 2012 in The American Journal of Human Genetics
Verified
Journal Article
Closed access
EKEsther Kott
Esther Kott
PDPhilippe Duquesnoy
Philippe Duquesnoy
BCBruno Copin
Bruno Copin
MLMarie Legendre
Marie Legendre
FMFlorence Dastot-Le Moal
Florence Dastot-Le Moal
SASerge Amselem
Serge Amselem

1 March 1998 in Journal of Biological Chemistry
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Journal Article
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Aminata TouréAminata Touré
Aminata Touré
ODOlivier Dorseuil
Olivier Dorseuil
LMLaurence Morin
Laurence Morin
PTPaula Timmons
Paula Timmons
BJBernard Jégou
Bernard Jégou
GGGérard Gacon
Gérard Gacon
In a search for new partners of the activated form of Rac GTPase, we have isolated through a two-hybrid cloning procedure a human cDNA encoding a new GTPase-activating protein (GAP) for Rho family GTPases. A specific mRNA of 3.2 kilobases was detected in low abundance in many cell types and found highly expressed in testis. A protein of the predicted size 58 kDa, which we call MgcRacGAP, was detected in human testis as well as in germ cell tumor extracts by immunoblotting with antibodies specific to recombinant protein. In vitro, the GAP domain of MgcRacGAP strongly stimulates Rac1 and Cdc42 GTPase activity but is almost inactive on RhoA. N-terminal to its GAP domain, MgcRacGAP contains a cysteine-rich zinc finger-like motif characteristic of the Chimaerin family of RhoGAPs. The closest homolog of MgcRacGAP is RotundRacGAP, a product of the Drosophila rotund locus. In situhybridization experiments in human testis demonstrate a specific expression of mgcRacGAP mRNA in spermatocytes similar to that of rotundRacGAP in Drosophila testis. Therefore, protein sequence similarity and analogous developmental and tissue specificities of gene expression support the hypothesis that RotundRacGAP and MgcRacGAP have equivalent functions in insect and mammalian germ cells. Since rotundRacGAP deletion leads to male sterility in the fruit fly, the mgcRacGAP gene may prove likewise to play a key role in mammalian male fertility.