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Niessing, D. ; Jansen, R.P.* ; Pohlmann, T* ; Feldbrügge, M.*

mRNA transport in fungal top models.

Wiley Interdiscip. Rev. RNA 9, DOI: 10.1002/wrna.1453 (2017)
Verlagsversion DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Eukaryotic cells rely on the precise determination of when and where proteins are synthesized. Spatiotemporal expression is supported by localization of mRNAs to specific subcellular sites and their subsequent local translation. This holds true for somatic cells as well as for oocytes and embryos. Most commonly, mRNA localization is achieved by active transport of the molecules along the actin or microtubule cytoskeleton. Key factors are molecular motors, adaptors, and RNA-binding proteins that recognize defined sequences or structures in cargo mRNAs. A deep understanding of this process has been gained from research on fungal model systems such as Saccharomyces cerevisiae and Ustilago maydis. Recent highlights of these studies are the following: (1) synergistic binding of two RNA-binding proteins is needed for high affinity recognition; (2) RNA sequences undergo profound structural rearrangements upon recognition; (3) mRNA transport is tightly linked to membrane trafficking; (4) mRNAs and ribosomes are transported on the cytoplasmic surface of endosomes; and (5) heteromeric protein complexes are, most likely, assembled co-translationally during endosomal transport. Thus, the study of simple fungal model organisms provides valuable insights into fundamental mechanisms of mRNA transport boosting the understanding of similar events in higher eukaryotes. For further resources related to this article, please visit the WIREs website.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Cis-acting Determinants; Early Endosome Motility; Binding Protein Rrm4; Ustilago-maydis; Saccharomyces-cerevisiae; Endoplasmic-reticulum; Candida-albicans; Poly(a)-binding Protein; Pathogenic Development; Localization Elements
Sprache englisch
Veröffentlichungsjahr 2017
HGF-Berichtsjahr 2017
ISSN (print) / ISBN 1757-7004
e-ISSN 1757-7012
Quellenangaben Band: 9, Heft: 1 Seiten: , Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Malden, MA
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-503091-001
PubMed ID 28994236
Scopus ID 85031120178
Erfassungsdatum 2017-10-20