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Down-regulation of RpS21, a putative translation initiation factor interacting with P40, produces viable minute imagos and larval lethality with overgrown hematopoietic organs and imaginal discs.

Abstract
Down-regulation of the Drosophila ribosomal protein S21 gene (rpS21) causes a dominant weak Minute phenotype and recessively produces massive hyperplasia of the hematopoietic organs and moderate overgrowth of the imaginal discs during larval development. Here, we show that the S21 protein (RpS21) is bound to native 40S ribosomal subunits in a salt-labile association and is absent from polysomes, indicating that it acts as a translation initiation factor rather than as a core ribosomal protein. RpS21 can interact strongly with P40, a ribosomal peripheral protein encoded by the stubarista (sta) gene. Genetic studies reveal that P40 underexpression drastically enhances imaginal disc overgrowth in rpS21-deficient larvae, whereas viable combinations between rpS21 and sta affect the morphology of bristles, antennae, and aristae. These data demonstrate a strong interaction between components of the translation machinery and showed that their underexpression impairs the control of cell proliferation in both hematopoietic organs and imaginal discs.
AuthorsI Török, D Herrmann-Horle, I Kiss, G Tick, G Speer, R Schmitt, B M Mechler
JournalMolecular and cellular biology (Mol Cell Biol) Vol. 19 Issue 3 Pg. 2308-21 (Mar 1999) ISSN: 0270-7306 [Print] United States
PMID10022917 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA, Complementary
  • Drosophila Proteins
  • Insect Proteins
  • Peptide Initiation Factors
  • Ribosomal Proteins
  • ribosomal protein S21
  • sta protein, Drosophila
Topics
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • DNA, Complementary
  • Down-Regulation
  • Drosophila Proteins
  • Drosophila melanogaster (growth & development, metabolism)
  • Gene Dosage
  • Humans
  • Insect Proteins (genetics, metabolism)
  • Larva
  • Molecular Sequence Data
  • Peptide Initiation Factors (genetics, metabolism)
  • Phenotype
  • Ribosomal Proteins (genetics, metabolism)
  • Sequence Homology, Amino Acid

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