Identification of the cis-elements mediating the autogenous control of ribosomal protein L2 mRNA stability in yeast

• Published in: The EMBO journal Vol. 14; no. 16; pp. 4022 - 4030
• Main Authors: Presutti, C, Villa, T, Hall, D, Pertica, C, Bozzoni, I
• Format: Journal Article
• Language: English
• Published: England 15-08-1995
• Subjects: alternative splicing; Base Sequence; beta-Galactosidase - genetics; Endoribonucleases - metabolism; Escherichia coli; Exoribonucleases - metabolism; Feedback; Gene Expression Regulation, Fungal - genetics; genetic regulation; Introns - genetics; messenger RNA; Molecular Sequence Data; nucleotide sequences; Poly G; post-transcriptional regulation; proteins; Recombinant Fusion Proteins - biosynthesis; Recombinant Fusion Proteins - metabolism; regulatory regions; Regulatory Sequences, Nucleic Acid - genetics; Ribosomal Proteins - genetics; ribosomes; RNA Precursors - metabolism; RNA Processing, Post-Transcriptional - genetics; RNA Splicing; RNA, Fungal - genetics; RNA, Fungal - metabolism; RNA, Messenger - genetics; RNA, Messenger - metabolism; Saccharomyces cerevisiae; Saccharomyces cerevisiae - genetics; Sequence Deletion; stability
• ISSN: 0261-4189; 1460-2075
• DOI: 10.1002/j.1460-2075.1995.tb00073.x

The ribosomal protein L2 (rpL2) of Saccharomyces cerevisiae regulates the accumulation of its own mRNA by a feedback mechanism. An RNA sequence is responsible for this control, initially characterized as a 360 nucleotide-long region, localized at the 5' end of the transcript. This region, fused to an unrelated coding sequence, is able to down-regulate the accumulation of the chimeric transcript when increased levels of rpL2 are induced in the cell. The target regulatory region also responds to regulation when inserted inside an intron, demonstrating that the control process can take place inside the nucleus. Deletion analysis from the 5' and 3' borders have restricted the responsive region to approximately 200 nt. The insertion of a poly-G cassette downstream of the regulatory region allowed the identification of truncated 3' cut-off poly(A)+ RNA molecules. The parallel identification of cut-off molecules containing the 5' portion of the transcript allowed us to deduce that the truncated products originate by endonucleolytic cleavage. Altogether, these results are consistent with a mechanism by which the presence of excess amounts of rpL2 in the cell triggers its own mRNA to a degradative pathway; this involves an initial endonucleolytic cleavage that is followed by exonucleolytic trimming. Such a regulatory mechanism shows interesting analogies with the translational regulation of r-proteins in Escherichia coli.