To identify Saccharomyces cerevisiae mutants defective in assembly or function of ribosomes, a collection of cold-sensitive strains generated by treatment with ethyl methanesulfonate was screened by sucrose gradient analysis for altered ratios of free 40S to 60S ribosomal subunits or qualitative changes in polyribosome profiles. Mutations The eukaryotic ribosome is a complex organelle which in most species contains more than 75 different proteins and four different RNA molecules. The primary sequences of eukaryotic rRNAs and many eukaryotic ribosomal proteins (r-proteins) (reviewed in references 65 and 66) have been determined or inferred from sequences of the respective genes. Regulation of expression of these genes has been studied in some detail (65,66). Despite the large volume of data concerning the structure and expression of individual components of eukaryotic ribosomes, the pathway of assembly of ribosomal subunits and the functional roles that r-proteins and rRNAs play during the translation process are not well understood.Ribosome biogenesis occurs in the nucleolus of eukaryotic cells, where rRNA is transcribed and processed, and associates with r-proteins imported from the cytoplasm (reviewed in references 19, 65, and 66). Preribosomal particles containing rRNA precursors, r-proteins, and non-r-proteins have been detected within the nucleolus (59, 63). Most of the r-proteins assemble into subunits while in the nucleolus, although some final steps of maturation occur after transport of subunits to the cytoplasm (61). The ribosomal subunits are then competent to catalyze protein synthesis.Reconstitution and genetic studies have been applied successfully to study the ribosome assembly pathway in prokaryotic cells. Functional 30S and 50S ribosomal subunits of Escherichia coli can be reconstituted from purified rRNA and r-proteins in vitro (38,60