Interrelations between the maturation of a 100 kDa nucleolar protein and pre rRNA synthesis in CHO cells (original) (raw)
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Centre de Recherche de Biochimie et de Génétique Cellulaires du CNRS
118, route de Narbonne, 31062 Toulouse Cedex, France
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Michèle Caizergues-Ferrer
Centre de Recherche de Biochimie et de Génétique Cellulaires du CNRS
118, route de Narbonne, 31062 Toulouse Cedex, France
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Centre de Recherche de Biochimie et de Génétique Cellulaires du CNRS
118, route de Narbonne, 31062 Toulouse Cedex, France
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Centre de Recherche de Biochimie et de Génétique Cellulaires du CNRS
118, route de Narbonne, 31062 Toulouse Cedex, France
*To whom correspondance should be addressed
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13 February 1984
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Gérard Bouche, Michèle Caizergues-Ferrer, Béatrix Bugler, François Amalric, Interrelations between the maturation of a 100 kDa nucleolar protein and pre rRNA synthesis in CHO cells, Nucleic Acids Research, Volume 12, Issue 7, 11 April 1984, Pages 3025–3035, https://doi.org/10.1093/nar/12.7.3025
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Abstract
The synthesis of preribosomal RNA is inhibited “in vivo” and “in vitro” by the protease inhibitor leupeptin. “In vivo” leupeptin decreases by 74 % the incorporation of labeled uridine into 45S pre rRNA while the synthesis of other RNA species is only slightly decreased. “In vitro”, the elongation of already initiated pre rRNA chains that is achieved by incubation of isolated nucleoli is blocked by leupeptin. On the other hand, “in vitro” leupeptin has no direct effect on RNA polymerase I, tested in a nonspecific transcriptional system with Calf thymus DNA as template and in run off experiments with a cloned DNA containing the initiation site of the rDNA gene. A 100 kDa nucleolar protein which has been shown to be endoproteolytic cleaved “in vivo” (1) acts as an inhibitor of rDNA transcription in presence of leupeptin but produces little effect on the nonspecific transcription. In absence of the drug, the 100 kDa protein is processed in specific peptides which appeared to be similar to the “in vivo” maturation products. The possible role of the 100 kDa maturation process in the regulation of rDNA transcription is discussed.
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© 1984 IRL Press Ltd.
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