Tgs1 is the hypermethylase responsible for m(3)G cap formation of U small nuclear RNAs (U snRNAs) and small nucleolar RNAs (snoRNAs). In vertebrates, hypermethylation of snRNAs occurs in the cytoplasm, whereas this process takes place in the nucleus for snoRNAs. Accordingly, the hypermethylase is found in both compartments with a diffuse localization in the cytoplasm and a concentration in Cajal bodies in the nucleoplasm. In this study, we report that the Tgs1 hypermethylase exists as two species, a full-length cytoplasmic isoform and a shorter nuclear isoform of 65-70 kDa. The short isoform exhibits methyltransferase activity and associates with components of box C/D and H/ACA snoRNPs, pointing to a role of this isoform in hypermethylation of snoRNAs. We also show that production of the short Tgs1 isoform is inhibited by MG132, suggesting that it results from proteasomal limited processing of the full-length Tgs1 protein. Together, our results suggest that proteasome maturation constitutes a mechanism regulating Tgs1 function by generating Tgs1 species with different substrate specificities, subcellular localizations, and functions.
Characterization of a short isoform of human Tgs1 hypermethylase associating with small nucleolar ribonucleoprotein core proteins and produced by limited proteolytic processing
Girard, C.; Verheggen, C.; Neel, H.; Cammas, A.; Vagner, S.; Soret, J.; Bertrand, E.; Bordonne, R.
J Biol Chem
2008-01-25 / vol 283 / pages 2060-9
IGMM team(s) involved in this publication
Biogenèse des ARNs
Assemblage et Trafic de Ribonucléoprotéines
Humans; Antineoplastic Agents/pharmacology; Hela Cells; Isoenzymes/genetics/metabolism; Cell Nucleus/*enzymology/genetics; Cytoplasm/enzymology/genetics; Leupeptins/pharmacology; Methylation/drug effects; Proteasome Endopeptidase Complex/genetics/*metabolism; RNA Caps/genetics/*metabolism; RNA Processing, Post-Transcriptional/drug effects/*physiology; RNA, Small Nuclear/genetics/*metabolism; tRNA Methyltransferases/genetics/*metabolism