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Tag‐mediated fractionation of yeast ribosome populations proves the monomeric organization of the eukaryotic ribosomal stalk structure
Author(s) -
Guarinos Esther,
Santos Cruz,
Sánchez Arancha,
Qiu DeYi,
Remacha Miguel,
Ballesta Juan P. G.
Publication year - 2003
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.2003.03733.x
Subject(s) - biology , stalk , ribosome , yeast , ribosomal rna , eukaryotic cell , genetics , microbiology and biotechnology , computational biology , evolutionary biology , rna , gene , horticulture
Summary The analysis of the not well understood composition of the stalk, a key ribosomal structure, in eukaryotes having multiple 12 kDa P1/P2 acidic protein components has been approached using these proteins tagged with a histidine tail at the C‐terminus. Tagged Saccharomyces cerevisiae ribosomes, which contain two P1 proteins (P1α and P1β) and two P2 proteins (P2α and P2β), were fractionated by affinity chromatography and their stalk composition was determined. Different yeast strains expressing one or two tagged proteins and containing either a complete or a defective stalk were used. No indication of protein dimers was found in the tested strains. The results are only compatible with a stalk structure containing a single copy of each one of the four 12 kDa proteins per ribosome. Ribosomes having an incomplete stalk are found in wild‐type cells. When one of the four proteins is missing, the ribosomes do not carry the three remaining proteins simultaneously, containing only two of them distributed in pairs made of one P1 and one P2. Ribosomes can carry two, one or no acidic protein pairs. The P1α/P2β and P1β/P2α pairs are preferentially found in the ribosome, but they are not essential either for stalk assembly or function.