F
Françoise Stutz
Researcher at University of Geneva
Publications - 66
Citations - 6763
Françoise Stutz is an academic researcher from University of Geneva. The author has contributed to research in topics: Nuclear pore & Transcription (biology). The author has an hindex of 37, co-authored 64 publications receiving 6464 citations. Previous affiliations of Françoise Stutz include Swiss National Science Foundation & University Hospital of Lausanne.
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Journal ArticleDOI
Bidirectional promoters generate pervasive transcription in yeast
Zhenyu Xu,Wu Wei,Julien Gagneur,Fabiana Perocchi,Sandra Clauder-Münster,Jurgi Camblong,Elisa Guffanti,Françoise Stutz,Wolfgang Huber,Lars M. Steinmetz +9 more
TL;DR: It is shown that both SUTs and CUTs display distinct patterns of distribution at specific locations, changing the view of how a genome is transcribed and indicating that bidirectionality is an inherent feature of promoters.
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The importin-beta family member Crm1p bridges the interaction between Rev and the nuclear pore complex during nuclear export
TL;DR: Viable mis-sense mutations in the CRM1 gene substantially reduced or eliminated the biological activity of Rev in S. cerevisiae, providing strong evidence that Crm1p also contributes to transport of Rev NES-containing proteins and ribonucleoproteins in this organism.
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Antisense RNA stabilization induces transcriptional gene silencing via histone deacetylation in S. cerevisiae
TL;DR: The data indicate that the stabilization of antisense transcripts results in PHO84 gene repression via a mechanism distinct from transcription interference and that the modulation of Rrp6 function contributes to gene regulation by inducing RNA-dependent epigenetic modifications.
Journal ArticleDOI
REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.
Françoise Stutz,Angela Bachi,Tobias Doerks,Isabelle C. Braun,Bertrand Séraphin,Matthias Wilm,Peer Bork,Elisa Izaurralde +7 more
TL;DR: Yra1p and members of the REF family of hnRNP-like proteins may facilitate the interaction of TAP/Mex67p with cellular mRNAs, which is likely to be mediated by protein-protein interactions.
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Stable mRNP Formation and Export Require Cotranscriptional Recruitment of the mRNA Export Factors Yra1p and Sub2p by Hpr1p
TL;DR: The data indicate that transcription and export are functionally linked and that mRNA export defects may be due in part to inefficient loading of essential mRNA export factors on the growing mRNP.