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来自培养肌肉细胞的多核糖体:肌球蛋白的无细胞合成

Polysomes from cultured muscle cells: the cell-free synthesis of myosin.

作者信息

Tepperman K, Essien F, Heywood S M

出版信息

J Cell Physiol. 1975 Dec;86(3 Pt 1):553-60. doi: 10.1002/jcp.1040860312.

DOI:10.1002/jcp.1040860312
PMID:811675
Abstract

The results reported here have shown that there are significant differences between polysome patterns obtained from cultured cells and from freshly isolated muscle tissue. Polysomes from embryonic homogenates show different patterns with different levels of myosin synthesis, but this does not appear to be the case with cultured cells. Experiments utilizing cell-free protein synthesizing systems indicate that the polysomes isolated from myoblast cultures can synthesize myosin at levels similar to those obtained from myotube cultures, suggesting that the myoblasts contain significant amounts of the messenger RNA for myosin. In contrast, the polysomes isolated from BrdUrd-inhibited cultures synthesize a comparatively low level of myosin. These findings illustrate a significant difference between myoblasts and BrdUrd-inhibited cells.

摘要

此处报告的结果表明,从培养细胞和新鲜分离的肌肉组织中获得的多核糖体模式存在显著差异。胚胎匀浆中的多核糖体显示出不同的模式以及不同水平的肌球蛋白合成,但培养细胞似乎并非如此。利用无细胞蛋白质合成系统进行的实验表明,从成肌细胞培养物中分离出的多核糖体能够以与从肌管培养物中获得的水平相似的水平合成肌球蛋白,这表明成肌细胞含有大量的肌球蛋白信使核糖核酸。相比之下,从溴脱氧尿苷抑制的培养物中分离出的多核糖体合成的肌球蛋白水平相对较低。这些发现说明了成肌细胞与溴脱氧尿苷抑制细胞之间的显著差异。

相似文献

1
Polysomes from cultured muscle cells: the cell-free synthesis of myosin.来自培养肌肉细胞的多核糖体:肌球蛋白的无细胞合成
J Cell Physiol. 1975 Dec;86(3 Pt 1):553-60. doi: 10.1002/jcp.1040860312.
2
Stimulation of myosin heavy chain synthesis in steady-state muscle cultures by the ionophore, A23187, requires transcription of messenger RNA.在稳定状态的肌肉培养物中,离子载体A23187对肌球蛋白重链合成的刺激需要信使核糖核酸的转录。
Eur J Cell Biol. 1981 Dec;26(1):184-7.
3
Isolation of myosin-synthesizing polysomes from cultures of embryonic chicken myoblasts before fusion.在胚胎鸡成肌细胞融合前的培养物中分离合成肌球蛋白的多核糖体。
Dev Biol. 1975 Nov;47(1):123-35. doi: 10.1016/0012-1606(75)90268-7.
4
[Myosin isoenzymes during in vivo and in vitro differentiation of chick muscles].
C R Seances Acad Sci D. 1980 Jan 21;290(3):223-6.
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Expression of aldolase A steady-state mRNA is delayed relative to other muscle-specific genes during differentiation of chicken myoblasts.在鸡成肌细胞分化过程中,醛缩酶A稳态mRNA的表达相对于其他肌肉特异性基因延迟。
Exp Cell Res. 1995 Sep;220(1):55-61. doi: 10.1006/excr.1995.1291.
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Normal and dystrophic embryonic chicken pectoralis muscle cultures: I. Cell differentiation, protein synthesis, and enzyme levels.正常和营养不良的胚胎鸡胸肌培养物:I. 细胞分化、蛋白质合成和酶水平。
Muscle Nerve. 1981 Mar-Apr;4(2):117-24. doi: 10.1002/mus.880040207.
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Myosin heavy chain messenger RNA from myogenic cell cultures.来自成肌细胞培养物的肌球蛋白重链信使核糖核酸
Proc Natl Acad Sci U S A. 1974 Mar;71(3):662-6. doi: 10.1073/pnas.71.3.662.
8
Quantification of myosin heavy-chain mRNA during myogenesis.成肌过程中肌球蛋白重链mRNA的定量分析。
Eur J Biochem. 1978 Jan 16;82(2):601-8. doi: 10.1111/j.1432-1033.1978.tb12056.x.
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Expression of gap junctions in cultured rat L6 cells during myogenesis.大鼠L6细胞在成肌过程中缝隙连接的表达。
Dev Biol. 1993 Feb;155(2):351-60. doi: 10.1006/dbio.1993.1034.
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Effect of creatine on contents of myosin heavy chain and myosin-heavy-chain mRNA in steady-state chicken muscle-cell cultures.肌酸对稳态鸡肌细胞培养物中肌球蛋白重链及肌球蛋白重链mRNA含量的影响
Biochem J. 1984 Mar 15;218(3):871-6. doi: 10.1042/bj2180871.

引用本文的文献

1
Intact microtubules are required for rapid turnover of carboxyl-terminal tyrosine of alpha-tubulin in cell cultures.完整的微管对于细胞培养中α-微管蛋白羧基末端酪氨酸的快速周转是必需的。
Proc Natl Acad Sci U S A. 1979 Mar;76(3):1318-22. doi: 10.1073/pnas.76.3.1318.