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A high-throughput siRNA screen identifies genes that regulate mannose 6-phosphate receptor trafficking

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F14%3A00078588" target="_blank" >RIV/00216224:14110/14:00078588 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1242/jcs.159608" target="_blank" >http://dx.doi.org/10.1242/jcs.159608</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1242/jcs.159608" target="_blank" >10.1242/jcs.159608</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A high-throughput siRNA screen identifies genes that regulate mannose 6-phosphate receptor trafficking

  • Original language description

    The delivery of newly synthesized soluble lysosomal hydrolases to the endosomal system is essential for lysosome function and cell homeostasis. This process relies on the proper trafficking of the mannose 6-phosphate receptors (MPRs) between the trans-Golgi network (TGN), endosomes and the plasma membrane. Many transmembrane proteins regulating diverse biological processes ranging from virus production to the development of multicellular organisms also use these pathways. To explore how cell signaling modulates MPR trafficking, we used high-throughput RNA interference (RNAi) to target the human kinome and phosphatome. Using high-content image analysis, we identified 127 kinases and phosphatases belonging to different signaling networks that regulate MPR trafficking and/or the dynamic states of the subcellular compartments encountered by the MPRs. Our analysis maps the MPR trafficking pathways based on enzymes regulating phosphatidylinositol phosphate metabolism.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Cell Science

  • ISSN

    0021-9533

  • e-ISSN

  • Volume of the periodical

    127

  • Issue of the periodical within the volume

    23

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    14

  • Pages from-to

    5079-5092

  • UT code for WoS article

    000345896800009

  • EID of the result in the Scopus database