Arbusov V A
Vopr Med Khim. 1979 Jan-Feb;25(1):62-7.
Actinomycin D caused degradation of mRNA both in membrane-bound and in free polyribosomes from rat liver cells. The rate of mRNA destruction was distinctly higher in free polyribosomes, than in membrane-bound ones. Cycloheximide inhibited the mRNA destruction in both types of polyribosomes. At the same time, the stabilizing effect of cycloheximide on mRNA was less distinct in free polyribosomes. A decrease in specific radioactivity of mRNA from membrane-bound and free polyribosomes was observed after prolonged pretreatment with actinomycin D. The specific radioactivity of mRNA from polyribosomes of both types was not altered after simultaneous administration of actinomycin D and cycloheximide into rats. Occurence of two fractions of mRNA, dissimilar in stability, is possible both in membrane-bound and in free polyribosomes from rat liver cells.
放线菌素D可导致大鼠肝细胞中膜结合型和游离多核糖体中的mRNA降解。游离多核糖体中mRNA的破坏速率明显高于膜结合型多核糖体。环己酰亚胺抑制了两种类型多核糖体中的mRNA破坏。同时,环己酰亚胺对游离多核糖体中mRNA的稳定作用不太明显。用放线菌素D长时间预处理后,观察到膜结合型和游离多核糖体中mRNA的比放射性降低。将放线菌素D和环己酰亚胺同时给大鼠注射后,两种类型多核糖体中mRNA的比放射性没有改变。大鼠肝细胞的膜结合型和游离多核糖体中都可能存在稳定性不同的两种mRNA组分。