PUBLICATION

Physical and Functional Interaction between Pes1 and Bop1 in Mammalian Ribosome Biogenesis

Authors
Lapik, Y.R., Fernandes, C.J., Lau, L.F., and Pestov, D.G.
ID
ZDB-PUB-040701-1
Date
2004
Source
Molecular Cell   15(1): 17-29 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Amino Acid Sequence/genetics
  • Animals
  • Base Sequence/genetics
  • Cell Cycle/genetics
  • Cell Differentiation/genetics
  • Cell Line
  • DNA Transposable Elements/genetics
  • Mammals/genetics
  • Mammals/metabolism*
  • Mice
  • Molecular Sequence Data
  • Nuclear Proteins/genetics
  • Nuclear Proteins/metabolism*
  • Proteins/genetics
  • Proteins/metabolism*
  • RNA, Ribosomal/biosynthesis
  • RNA, Ribosomal/genetics
  • Ribosomes/genetics
  • Ribosomes/metabolism*
PubMed
15225545 Full text @ Mol. Cell
Abstract
Molecular mechanisms of mammalian ribosome biogenesis remain largely unexplored. Here we develop a series of transposon-derived dominant mutants of Pes1, the mouse homolog of the zebrafish Pescadillo and yeast Nop7p implicated in ribosome biogenesis and cell proliferation control. Six Pes1 mutants selected by their ability to reversibly arrest the cell cycle also impair maturation of the 28S and 5.8S rRNAs in mouse cells. We show that Pes1 physically interacts with the nucleolar protein Bop1, and both proteins direct common pre-rRNA processing steps. Interaction with Bop1 is essential for the efficient incorporation of Pes1 into nucleolar preribosomal complexes. Pes1 mutants defective for the interaction with Bop1 lose the ability to affect rRNA maturation and the cell cycle. These data show that coordinated action of Pes1 and Bop1 is necessary for the biogenesis of 60S ribosomal subunits.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping