TY - JOUR
T1 - 90S pre-ribosomes include the 35S pre-rRNA, the U3 snoRNP, and 40S subunit processing factors but predominantly lack 60S synthesis factors
AU - Grandi, Paola
AU - Rybin, Vladimir
AU - Baßler, Jochen
AU - Petfalski, Elisabeth
AU - Strauß, Daniela
AU - Marzioch, Martina
AU - Schäfer, Thorsten
AU - Kuster, Bernhard
AU - Tschochner, Herbert
AU - Tollervey, David
AU - Gavin, Anne Claude
AU - Hurt, Ed
N1 - Funding Information:
We are grateful to Dr. Y. Kikuchi (University of Tokyo, Bunkyo-ku, Tokyo, Japan) for sending us the krr1- ts mutants. We thank all members of the yeast group, the bioinformatic and mass spectrometry departments at Cellzome for their excellent contribution to this work. We thank C. Cohen, S. Artavanis, G. Superti-Furga, G. Neubauer, and T. Bouwmeester for support. E.H. was supported by grants from the Deutsche Forschungsgemeinschaft and Fonds der Chemischen Industrie. E.P. and D.T. were supported by the Wellcome Trust.
PY - 2002
Y1 - 2002
N2 - We report the characterization of early pre-ribosomal particles. Twelve TAP-tagged components each showed nucleolar localization, sedimented at approximately 90S on sucrose gradients, and coprecipitated both the 35S pre-rRNA and the U3 snoRNA. Thirty-five non-ribosomal proteins were coprecipitated, including proteins associated with U3 (Nop56p, Nop58p, Sof1p, Rrp9, Dhr1p, Imp3p, Imp4p, and Mpp10p) and other factors required for 18S rRNA synthesis (Nop14p, Bms1p, and Krr1p). Mutations in components of the 90S pre-ribosomes impaired 40S subunit assembly and export. Strikingly, few components of recently characterized pre-60S ribosomes were identified in the 90S pre-ribosomes. We conclude that the 40S synthesis machinery predominately associates with the 35S pre-rRNA factors, whereas factors required for 60S subunit synthesis largely bind later, showing an unexpected dichotomy in binding.
AB - We report the characterization of early pre-ribosomal particles. Twelve TAP-tagged components each showed nucleolar localization, sedimented at approximately 90S on sucrose gradients, and coprecipitated both the 35S pre-rRNA and the U3 snoRNA. Thirty-five non-ribosomal proteins were coprecipitated, including proteins associated with U3 (Nop56p, Nop58p, Sof1p, Rrp9, Dhr1p, Imp3p, Imp4p, and Mpp10p) and other factors required for 18S rRNA synthesis (Nop14p, Bms1p, and Krr1p). Mutations in components of the 90S pre-ribosomes impaired 40S subunit assembly and export. Strikingly, few components of recently characterized pre-60S ribosomes were identified in the 90S pre-ribosomes. We conclude that the 40S synthesis machinery predominately associates with the 35S pre-rRNA factors, whereas factors required for 60S subunit synthesis largely bind later, showing an unexpected dichotomy in binding.
UR - http://www.scopus.com/inward/record.url?scp=18544371820&partnerID=8YFLogxK
U2 - 10.1016/S1097-2765(02)00579-8
DO - 10.1016/S1097-2765(02)00579-8
M3 - Article
AN - SCOPUS:18544371820
SN - 1097-2765
VL - 10
SP - 105
EP - 115
JO - Molecular Cell
JF - Molecular Cell
IS - 1
ER -