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[大鼠肝脏再生不同阶段细胞中蛋白质合成与信使核糖核酸核质运输之间的相互关系]

[Interrelation between protein synthesis and nucleo-cytoplasmic transport of messenger RNA in cells of rat livers in different stages of regeneration].

作者信息

Arbuzov V A, Del'vig A A

出版信息

Vopr Med Khim. 1981;27(4):552-9.

PMID:7293087
Abstract

Synthesis of nonribosomal RNA was increased 2-2.5-fold in nuclei of rat liver cells at early steps of regeneration /2 days after partial hepatectomy/under conditions of protein synthesis inhibition by means of cycloheximide within 3 hrs. Amount of mRNA, transferred from nuclei into cytoplasm, was also 2-fold higher under these conditions as compared with control cells. The mRNA, transferred from nuclei into cytoplasm under the conditions of cycloheximide treatment of liver cells at early steps of regeneration, did penetrate the polyribosomes although the protein synthesis did not occur on the polyribosomes formed. At the later steps of regeneration /within 5 days after partial hepatectomy/ under the conditions of protein synthesis inhibition by cycloheximide within 3 hrs, formation of nonribosomal RNA was decreased by 40% in liver cell nuclei; amount of mRNA, transferred into cytoplasm, was also decreased by 40%. When the cycloheximide treatment was carried out during 1 hr, synthesis of nonribosomal RNA was increased 1.5-fold in liver cell nuclei at the later steps of regeneration although the amount of mRNA, transferred from nuclei into cytoplasm, was decreased by 30% as compared with the control cells. The data obtained suggest that during rat liver tissue regeneration a change occurred in the molecular mechanisms linking translation, biosynthesis and nuclear-cytoplasmic transport of mRNA of "tumoral" type/at early steps of regeneration/ or "normal type"/ at later steps of regeneration.

摘要

在部分肝切除术后2天,大鼠肝细胞再生早期,在3小时内用环己酰亚胺抑制蛋白质合成的条件下,非核糖体RNA的合成在细胞核中增加了2至2.5倍。与对照细胞相比,在这些条件下从细胞核转移到细胞质中的mRNA量也高出2倍。在再生早期用环己酰亚胺处理肝细胞的条件下从细胞核转移到细胞质中的mRNA确实穿透了多核糖体,尽管在形成的多核糖体上没有发生蛋白质合成。在再生后期(部分肝切除术后5天内),在3小时内用环己酰亚胺抑制蛋白质合成的条件下,肝细胞核中非核糖体RNA的形成减少了40%;转移到细胞质中的mRNA量也减少了40%。当环己酰亚胺处理进行1小时时,在再生后期肝细胞核中非核糖体RNA的合成增加了1.5倍,尽管与对照细胞相比,从细胞核转移到细胞质中的mRNA量减少了30%。所获得的数据表明,在大鼠肝组织再生过程中,连接“肿瘤”型mRNA(在再生早期)或“正常”型mRNA(在再生后期)的翻译、生物合成和核质转运的分子机制发生了变化。

相似文献

1
[Interrelation between protein synthesis and nucleo-cytoplasmic transport of messenger RNA in cells of rat livers in different stages of regeneration].[大鼠肝脏再生不同阶段细胞中蛋白质合成与信使核糖核酸核质运输之间的相互关系]
Vopr Med Khim. 1981;27(4):552-9.
2
[Nucleo-cytoplasmic mRNA transport in liver rat and hepatoma cells following suppression of protein synthesis by cycloheximide].
Vopr Med Khim. 1980 May-Jun;26(3):354-61.
3
[Changes in the mechanisms controlling mRNA stability during the process of liver regeneration in rats].[大鼠肝脏再生过程中控制mRNA稳定性机制的变化]
Vopr Med Khim. 1980 Jul-Aug;26(4):517-25.
4
Analysis of gene expression in regenerating rat liver by hybridization of nuclear and cytoplasmic RNA with DNA.通过核RNA和细胞质RNA与DNA杂交分析再生大鼠肝脏中的基因表达。
Cancer Res. 1977 Jan;37(1):118-27.
5
Intracellular distribution of transglutaminase activity during rat liver regeneration.大鼠肝脏再生过程中转谷氨酰胺酶活性的细胞内分布
J Cell Physiol. 1982 Nov;113(2):252-6. doi: 10.1002/jcp.1041130211.
6
[Stabilization of polyribosomal mRNA in rat liver cells under protein synthesis inhibition by cycloheximide].[环己酰亚胺抑制蛋白质合成时大鼠肝细胞中多聚核糖体mRNA的稳定性]
Biokhimiia. 1978 May;43(5):838-50.
7
[The effect of cycloheximide on incorporation of newly formed mRNA into membrane-bound polyribosomes in rat liver cells].[放线菌酮对大鼠肝细胞中新合成的mRNA掺入膜结合多核糖体的影响]
Biokhimiia. 1976 Feb;41(2):304- 7.
8
[RNA biosynthesis in mitochondria under conditions of prolonged inhibition of protein biosynthesis in rat liver cytoplasm].[大鼠肝细胞质中蛋白质生物合成长期受抑制条件下线粒体中的RNA生物合成]
Mol Biol (Mosk). 1976 Nov-Dec;10(6):1238-48.
9
[The interaction between newly-formed mRNA and ribosomal particles during retarded translation].[延迟翻译过程中新合成的mRNA与核糖体颗粒之间的相互作用]
Mol Biol (Mosk). 1975 Nov-Dec;9(6):845-55.
10
[Control of RNA biosynthesis in rat liver. Some features of RNA biosynthesis during prolonged protein synthesis inhibition].[大鼠肝脏中RNA生物合成的调控。蛋白质合成长期抑制期间RNA生物合成的一些特征]
Biokhimiia. 1976 Oct;41(10):1859-70.