A novel multifunctional factor involved in trans-splicing of chloroplast introns in Chlamydomonas

Nucleic Acids Res. 2006 Jan 10;34(1):262-74. doi: 10.1093/nar/gkj429. Print 2006.

Abstract

In the chloroplast of Chlamydomonas reinhardtii, psaA mRNA is spliced in trans from three separate precursors which assemble to form two group II introns. A fourth transcript, tscA, completes the structure of the first intron. Of the fourteen nucleus-encoded factors involved in psaA splicing, only two are required for splicing of both introns. We cloned and characterized the first of these more general factors, Raa1. Consistently with its role in psaA splicing, Raa1 is imported in the chloroplast where it is found in a membrane fraction and is part of a large ribonucleoprotein complex. One mutant, raa1-L137H, is defective for splicing of both introns, but another allelic mutant, raa1-314B, still expresses the 3' part of the Raa1 gene and is deficient only in splicing of intron 2. This observation and a deletion analysis indicate the presence of two domains in Raa1. The C-terminal domain is necessary and sufficient for processing of tscA RNA and splicing of the first intron, while the central domain is essential for splicing of the second intron. The combination of these two functional domains in Raa1 suggests that this new factor may coordinate trans-splicing of the two introns to improve the efficiency of psaA maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algal Proteins / chemistry
  • Algal Proteins / genetics
  • Algal Proteins / physiology*
  • Alleles
  • Amino Acid Sequence
  • Animals
  • Chlamydomonas reinhardtii / genetics*
  • Chlamydomonas reinhardtii / metabolism
  • Chloroplasts / genetics*
  • Chloroplasts / metabolism
  • Cloning, Molecular
  • Introns*
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Molecular Sequence Data
  • Mutation
  • Protein Structure, Tertiary
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / physiology*
  • Repetitive Sequences, Amino Acid
  • Ribonucleases / metabolism
  • Trans-Splicing*

Substances

  • Algal Proteins
  • Membrane Proteins
  • Protozoan Proteins
  • RNA-Binding Proteins
  • tscA protein, Chlamydomonas
  • Ribonucleases

Associated data

  • GENBANK/AJ605114