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Activation of Protein Synthesis by Microsomes from Aging Beet Disks
Author(s) -
R. John Ellis,
I. R. MACDONALD
Publication year - 1967
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.42.9.1297
Subject(s) - microsome , cycloheximide , protein biosynthesis , messenger rna , puromycin , biochemistry , chloramphenicol , derepression , rna , rnase p , centrifugation , biology , chemistry , hydroxylamine , enzyme , gene , gene expression , psychological repression , antibiotics
Microsomal fractions isolated from sterile, aged disks of red beetroot incorporate leucine into protein when supplemented with the supernatant fraction, ATP, GTP, and KCl; the incorporation is sensitive to RNase and is not due to bacteria. The microsomal activity is inhibited by puromycin and cycloheximide but is virtually insensitive to both d-threo and l-threo-chloramphenicol, as predicted from physiological studies.Microsomes isolated from fresh disks have much lower incorporating ability than those from disks aged for 1 or 2 days; maximal activity occurs when the rate of protein synthesis by the intact disks is highest. The low activity of fractions from fresh disks is attributable to a deficiency in the microsomal fraction and not to the supernatant fraction; it is not due to a dissociable inhibitor. The RNA content of the microsomal fraction increases with aging and so the increase in incorporating ability may be due to a synthesis of messenger RNA induced by slicing, rather than to an activation of pre-existing messenger. These results support the view that the aging phenomenon involves a derepression of gene activity.

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