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  Systematic genetic interaction screens uncover cell polarity regulators and functional redundancy.

Fievet, B. T., Rodriguez, J., Naganathan, S., Lee, C., Zeiser, E., Ishidate, T., et al. (2013). Systematic genetic interaction screens uncover cell polarity regulators and functional redundancy. Nature Cell Biology, 15(1), 103-112.

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Fievet, Bruno Thomas, Autor
Rodriguez, Josana1, Autor
Naganathan, Sundar2, Autor           
Lee, Christine, Autor
Zeiser, Eva1, Autor
Ishidate, Takao1, Autor
Shirayama, Masaki1, Autor
Grill, Stephan W.2, Autor           
Ahringer, Julie, Autor
Affiliations:
1Max Planck Society, ou_persistent13              
2Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Although single-gene loss-of-function analyses can identify components of particular processes, important molecules are missed owing to the robustness of biological systems. Here we show that large-scale RNAi screening for suppression interactions with functionally related mutants greatly expands the repertoire of genes known to act in a shared process and reveals a new layer of functional relationships. We performed RNAi screens for 17 Caenorhabditis elegans cell polarity mutants, generating the most comprehensive polarity network in a metazoan, connecting 184 genes. Of these, 72% were not previously linked to cell polarity and 80% have human homologues. We experimentally confirmed functional roles predicted by the network and characterized through biophysical analyses eight myosin regulators. In addition, we discovered functional redundancy between two unknown polarity genes. Similar systematic genetic interaction screens for other biological processes will help uncover the inventory of relevant genes and their patterns of interactions.

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 Datum: 2013
 Publikationsstatus: Erschienen
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 Identifikatoren: eDoc: 688468
Anderer: 5088
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Titel: Nature Cell Biology
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 15 (1) Artikelnummer: - Start- / Endseite: 103 - 112 Identifikator: -