RNA-binding proteins of the L7Ae family are at the heart of many essential ribonucleoproteins (RNPs), including box C/D and H/ACA small nucleolar RNPs, U4 small nuclear RNP, telomerase, and messenger RNPs coding for selenoproteins. In this study, we show that Nufip and its yeast homologue Rsa1 are key components of the machinery that assembles these RNPs. We observed that Rsa1 and Nufip bind several L7Ae proteins and tether them to other core proteins in the immature particles. Surprisingly, Rsa1 and Nufip also link assembling RNPs with the AAA + adenosine triphosphatases hRvb1 and hRvb2 and with the Hsp90 chaperone through two conserved adaptors, Tah1/hSpagh and Pih1. Inhibition of Hsp90 in human cells prevents the accumulation of U3, U4, and telomerase RNAs and decreases the levels of newly synthesized hNop58, hNHP2, 15.5K, and SBP2. Thus, Hsp90 may control the folding of these proteins during the formation of new RNPs. This suggests that Hsp90 functions as a master regulator of cell proliferation by allowing simultaneous control of cell signaling and cell growth.
The Hsp90 chaperone controls the biogenesis of L7Ae RNPs through conserved machinery
Boulon, S.; Marmier-Gourrier, N.; Pradet-Balade, B.; Wurth, L.; Verheggen, C.; Jady, B. E.; Rothe, B.; Pescia, C.; Robert, M. C.; Kiss, T.; Bardoni, B.; Krol, A.; Branlant, C.; Allmang*, C.; Bertrand*, E.; Charpentier*, B.
J Cell Biol
2008-02-11 / vol 180 / pages 579-95
jcb.200708110 [pii] 10.1083/jcb.200708110
IGMM team(s) involved in this publication
Biogenèse des ARNs
Cell Proliferation; Molecular Chaperones/genetics/*metabolism; Evolution, Molecular; Saccharomyces cerevisiae Proteins/genetics/*metabolism; Saccharomyces cerevisiae/genetics/*metabolism; Nuclear Proteins/genetics/metabolism; Adenosine Triphosphatases/genetics/metabolism; Cell Cycle Proteins/genetics/metabolism; Conserved Sequence/genetics; DNA Helicases/genetics/metabolism; DNA-Binding Proteins/genetics/metabolism; Heterogeneous-Nuclear Ribonucleoprotein L/genetics/*metabolism; HSP90 Heat-Shock Proteins/genetics/*metabolism; Protein Binding/physiology; Protein Folding; RNA-Binding Proteins/genetics/metabolism; Signal Transduction/physiology