Ribosomal protein L1 recognizes the same specific structural motif in its target sites on the autoregulatory mRNA and 23S rRNA

Nucleic Acids Res. 2005 Jan 19;33(2):478-85. doi: 10.1093/nar/gki194. Print 2005.

Abstract

The RNA-binding ability of ribosomal protein L1 is of profound interest since the protein has a dual function as a ribosomal protein binding rRNA and as a translational repressor binding its mRNA. Here, we report the crystal structure of ribosomal protein L1 in complex with a specific fragment of its mRNA and compare it with the structure of L1 in complex with a specific fragment of 23S rRNA determined earlier. In both complexes, a strongly conserved RNA structural motif is involved in L1 binding through a conserved network of RNA-protein H-bonds inaccessible to the solvent. These interactions should be responsible for specific recognition between the protein and RNA. A large number of additional non-conserved RNA-protein H-bonds stabilizes both complexes. The added contribution of these non-conserved H-bonds makes the ribosomal complex much more stable than the regulatory one.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Homeostasis
  • Models, Molecular
  • Nucleic Acid Conformation
  • RNA, Archaeal / chemistry
  • RNA, Archaeal / metabolism
  • RNA, Messenger / chemistry*
  • RNA, Messenger / metabolism
  • RNA, Ribosomal, 23S / chemistry*
  • RNA, Ribosomal, 23S / metabolism
  • RNA-Binding Proteins / chemistry*
  • RNA-Binding Proteins / metabolism
  • Ribosomal Proteins / chemistry*
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / metabolism

Substances

  • RNA, Archaeal
  • RNA, Messenger
  • RNA, Ribosomal, 23S
  • RNA-Binding Proteins
  • Ribosomal Proteins
  • ribosomal protein L1

Associated data

  • PDB/1U63