Zlatopol'skiĭ A D
Biokhimiia. 1976 Feb;41(2):304- 7.
Incorporation kinetics of new synthesized mRNA into free and endoplasmic membrane-bound polyribosomes in the absence of normal translation (when protein synthesis in inhibited by 98% with cycloheximide) is studied. mRNA is found to incorporate into both free and bound polyribosomes. Relative content of new synthesized membrane-bound polyribosomes in the presence of cycloheximide within 2.5-4.5 hours is by 30-40% lower as compared with the control. This fact can be explained either by the absence of a growing peptide of a sufficient length, which is necessary for the formation of a part of membrane-bound polyribosomes, or by a restricted number of attachment sites on membranes as a result of delayed translation of mRNA in pre-existed polyribosomes. It is suggested that 1) the growing peptide in liver cells is responsible for the recognition of a membrane only under the formation of only one type of membrane-bound polyribosomes, or 2) the formation of all bound polyribosomes has a single mechanism and the growing peptide does not participates in the membrane recognition.
研究了在无正常翻译情况下(当蛋白质合成被环己酰亚胺抑制98%时)新合成的mRNA掺入游离和内质网膜结合多核糖体的动力学。发现mRNA可掺入游离和结合的多核糖体中。与对照相比,在2.5 - 4.5小时内,存在环己酰亚胺时新合成的膜结合多核糖体的相对含量低30 - 40%。这一事实可以解释为:要么是缺乏足够长度的正在生长的肽,而这是形成部分膜结合多核糖体所必需的;要么是由于预先存在的多核糖体中mRNA翻译延迟,导致膜上的附着位点数量受限。有人提出:1)肝细胞中正在生长的肽仅在形成一种类型的膜结合多核糖体时负责识别膜,或者2)所有结合多核糖体的形成具有单一机制,且正在生长的肽不参与膜识别。