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SsrA genes of streptomycetes and association of proteins to the tmRNA during development and cellular differentiation
Author(s) -
Mikulík Karel,
Palečková Petra,
Felsberg Jürgen,
Bobek Jan,
Zídková Jarmila,
Halada Petr
Publication year - 2008
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200700560
Subject(s) - biology , ribosome , rna , transfer rna , open reading frame , gene , genetics , ribosomal rna , ribosomal protein , ef tu , microbiology and biotechnology , biochemistry , peptide sequence
Transfer‐messenger RNA (tmRNA, 10Sa RNA, ssrA) is bacterial RNA having both tRNA and mRNA properties and playing an essential role in recycling of 70S ribosomes that are stalled on defective mRNA. The trans‐ translational system is thought to play a crucial role in bacterial survival under adverse conditions. Streptomycetes are Gram‐positive soil bacteria exposed to various physical and chemical stresses that activate specialized responses such as synthesis of antibiotics and morphological differentiation. Comparative sequence analysis of ssrA genes of streptomycetes revealed the most significant differences in the central parts of tag‐reading frames, in the stop codons and in the 15–34 nucleotide sequences following stop codons. A major challenge in understanding the interactions that control the function of tmRNA is the definition of protein interactions. Proteins from various phases of development of Streptomyces aureofaciens associated with tmRNA were analyzed. Using affinity chromatography on tmRNA‐Sepharose and photo cross‐linking experiments with [ 32 P]labeled tmRNA seven proteins, the β and β′‐subunits of DNA dependent RNA polymerase, polyribonucleotide nucleotidyltransferase (PNPase), ribosomal protein SS1, ATP‐binding cassette transporters, elongation factor Tu, and SmpB were identified among the proteins associated with tmRNA of S. aureofaciens. We examined the functional role of ribosomal protein SS1 in a defined in vitro trans‐ translation system. Our data show that the protein SS1 that structurally differs from S1 of Escherichia coli is required for translation of the tmRNA tag‐reading frame.