Modulation of cell morphogenesis by tousled-like kinase in the Drosophila follicle cell

Dev Dyn. 2015 Jul;244(7):852-65. doi: 10.1002/dvdy.24292. Epub 2015 Jun 22.

Abstract

Background: Tousled-like kinase (Tlk) is a conserved serine/threonine kinase regulating DNA replication, chromatin assembly, and DNA repair. Previous studies have suggested that Tlk is involved in cell morphogenesis in vitro. In addition, tlk genetically interact with Rho1, which encodes a key regulator of the cytoskeleton. However, whether Tlk plays a physiological role in cell morphogenesis and cytoskeleton rearrangement remains unknown.

Results: In tlk mutant follicle cells, area of the apical domain was reduced. The density of microtubules was increased in tlk mutant cells. The density of actin filaments was increased in the apical region and decreased in the basal region. Because area of the apical domain was reduced, we examined the levels of proteins located in the apical region by using immunofluorescence. The fluorescence intensities of two adherens junction proteins Armadillo (Arm) and DE-cadherin (DE-cad), atypical protein kinase C (aPKC), and Notch, were all increased in tlk mutant cells. The basolateral localized Discs large (Dlg) shifted apically in tlk mutant cells.

Conclusions: Increase of protein densities in the apical region might be resulted from disruption of the cytoskeleton and shrinkage of the apical domain. Together, these data suggest a novel role of Tlk in maintaining cell morphology, possibly through modulating the cytoskeleton.

Keywords: actin filament; cell polarity; cytoskeleton; microtubule; oogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Armadillo Domain Proteins / genetics
  • Armadillo Domain Proteins / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster
  • Microtubules / enzymology*
  • Microtubules / genetics
  • Morphogenesis / physiology*
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • ARM protein, Drosophila
  • Armadillo Domain Proteins
  • Cadherins
  • Drosophila Proteins
  • N protein, Drosophila
  • Receptors, Notch
  • Transcription Factors
  • shg protein, Drosophila
  • tlk protein, Drosophila
  • Protein Serine-Threonine Kinases
  • PKC-3 protein
  • Protein Kinase C