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海拉细胞中的RNA合成。高渗培养基中的模式及其与G2期前期合成的相似性。

RNA synthesis in HeLa cells. Pattern in hypertonic medium and its similarity to synthesis during G2-prophase.

作者信息

Pederson T, Robbins E

出版信息

J Cell Biol. 1970 Dec;47(3):734-44. doi: 10.1083/jcb.47.3.734.

Abstract

Interphase HeLa cells manifest a stepwise shutoff of RNA synthesis when the tonicity of the extracellular medium is gradually increased. Synthesis of heterogeneous nuclear RNA is most sensitive and is selectively inhibited at 1.5 times isotonicity (450 milliosmols/liter), while 45S ribosomal RNA synthesis is not affected significantly below 2.0 times isotonicity. Transfer RNA synthesis is least sensitive to increased osmolarity and is not completely inhibited until the electrolyte concentration of the medium is elevated to 2.8 times isotonicity. Although the transcription and methylation of 45S ribosomal precursor is unaffected at 1.5 times isotonicity, there is pronounced impairment of its processing into 32S and 18S RNA. Using a refined cell synchronization technique, we have been able to compare these effects of hypertonicity with the shutoff of RNA synthesis which occurs during the G(2)-prophase interval of the cell division cycle. In this case, as with random cells in hypertonic medium, a selective inhibition of heterogeneous nuclear RNA synthesis and slowed processing of 45S ribosomal RNA were found, whereas synthesis of 45S and transfer RNA continued unabated throughout G(2)-prophase. While it is known that RNA synthesis essentially ceases during metaphase, we have noted that transfer RNA synthesis continues in metaphase at 10-15% of the interphase rate, which is of particular interest in view of the relative resistance of this species to hypertonicity. The close correlation between the patterns of cessation of RNA synthesis at mitosis and during exposure to hypertonic medium supports our earlier contention that alteration of intracellular electrolyte levels provides a useful model for studying the mechanism of mitosis.

摘要

当细胞外培养基的张力逐渐增加时,间期的海拉细胞会呈现出RNA合成的逐步关闭。不均一核RNA的合成最为敏感,在等渗度的1.5倍(450毫渗摩尔/升)时被选择性抑制,而45S核糖体RNA的合成在等渗度的2.0倍以下时不受显著影响。转运RNA的合成对渗透压增加最不敏感,直到培养基的电解质浓度升高到等渗度的2.8倍时才被完全抑制。尽管45S核糖体前体的转录和甲基化在等渗度的1.5倍时不受影响,但其加工成32S和18S RNA的过程却有明显受损。使用一种精细的细胞同步技术,我们能够将高渗的这些效应与细胞分裂周期G2期 - 前期期间发生的RNA合成关闭进行比较。在这种情况下,与处于高渗培养基中的随机细胞一样,发现不均一核RNA合成受到选择性抑制,45S核糖体RNA的加工减缓,而45S和转运RNA的合成在整个G2期 - 前期持续不受影响。虽然已知RNA合成在中期基本停止,但我们注意到转运RNA的合成在中期仍以间期速率的10 - 15%继续进行,鉴于该物种对高渗的相对抗性,这一点特别令人感兴趣。有丝分裂期间和暴露于高渗培养基期间RNA合成停止模式之间的密切相关性支持了我们早期的观点,即细胞内电解质水平的改变为研究有丝分裂机制提供了一个有用的模型。

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