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A genomic multiprocess survey of machineries that control and link cell shape, microtubule organization, and cell-cycle progression

  • Veronika Graml
  • , Xenia Studera
  • , Jonathan L.D. Lawson
  • , Anatole Chessel
  • , Marco Geymonat
  • , Miriam Bortfeld-Miller
  • , Thomas Walter
  • , Laura Wagstaff
  • , Eugenia Piddini
  • , Rafael E. Carazo-Salas
  • University of Cambridge
  • University of Cambridge
  • ETH Zurich
  • General Guisan-Quai 38
  • PriceSpective Ltd
  • Institut Curie

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

35 Citations (Scopus)

Résumé

Understanding cells as integrated systems requiresthat we systematically decipher how single genesaffect multiple biological processes and how processes are functionally linked. Here, we used multiprocess phenotypic profiling, combining high-resolution 3D confocal microscopy and multiparametric image analysis, to simultaneously survey the fission yeast genome with respect to three key cellular processes: cell shape, microtubule organization, and cell-cycle progression. We identify, validate, and functionally annotate 262 genes controlling specific aspects of those processes. Of these, 62% had not been linked to these processes before and 35% are implicated in multiple processes. Importantly, we identify a conserved role for DNA-damage responses in controlling microtubule stability. In addition, we investigate how the processes are functionally linked. We show unexpectedly that disruption of cell-cycle progression does not necessarily affect cell size control and that distinct aspects of cell shape regulate microtubules and vice versa, identifying important systems-level links across these processes.

langue originaleAnglais
Pages (de - à)227-239
Nombre de pages13
journalDevelopmental Cell
Volume31
Numéro de publication2
Les DOIs
étatPublié - 27 oct. 2014
Modification externeOui

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