The Ca2+-dependent protease Calpain A regulates Cactus/I kappaB levels during Drosophila development in response to maternal Dpp signals

Mech Dev. 2009 Aug-Sep;126(8-9):737-51. doi: 10.1016/j.mod.2009.04.005. Epub 2009 May 13.

Abstract

Regulation of NF kappaB activity is central to many processes during development and disease. Activation of NF kappaB family members depends on degradation of inhibitory I kappaB proteins. In Drosophila, a nuclear gradient of the NF kappaB/c-rel protein Dorsal subdivides the embryonic dorsal-ventral axis, defining the extent and location of mesodermal and ectodermal territories. Activation of the Toll pathway directs Dorsal nuclear translocation by inducing proteosomal degradation of the I kappaB homologue Cactus. Another mechanism that impacts on Dorsal activation involves the Toll-independent pathway, which regulates constitutive Cactus degradation. We have shown that the BMP protein Decapentaplegic (Dpp) inhibits Cactus degradation independent of Toll. Here we report on a novel element of this pathway: the calcium-dependent protease Calpain A. Calpain A knockdowns increase Cactus levels, shifting the Dorsal gradient and dorsal-ventral patterning. As shown for mammalian I kappaB, this effect requires PEST sequences in the Cactus C-terminus, implying a conserved role for calpains. Alteration of Calpain A or dpp results in similar effects on Dorsal target genes. Epistatic analysis confirms Calpain A activity is regulated by Dpp, indicating that Dpp signals increase Cactus levels through Calpain A inhibition, thereby interfering with Dorsal activation. This mechanism may allow coordination of Toll, BMP and Ca(2+) signals, conferring precision to Dorsal-target expression domains.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / chemistry*
  • Calpain / chemistry*
  • Crosses, Genetic
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / physiology
  • Drosophila / embryology*
  • Drosophila Proteins / biosynthesis
  • Drosophila Proteins / physiology*
  • Drosophila melanogaster
  • Gene Expression Regulation, Developmental*
  • I-kappa B Proteins / metabolism*
  • Models, Biological
  • Phenotype
  • Phosphoproteins / biosynthesis
  • Phosphoproteins / physiology
  • RNA, Double-Stranded / chemistry
  • Signal Transduction
  • Toll-Like Receptors / metabolism

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • I-kappa B Proteins
  • Phosphoproteins
  • RNA, Double-Stranded
  • Toll-Like Receptors
  • dpp protein, Drosophila
  • cact protein, Drosophila
  • Calpain
  • Calcium