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紫外线照射及照射后培养对小鼠细胞中核不均一RNA大小的影响。

Effects of ultraviolet irradiation and postirradiation incubation on heterogenous nuclear RNA size in murine cells.

作者信息

Ali R, Sauerbier W

出版信息

Biophys J. 1978 Jun;22(3):393-411. doi: 10.1016/s0006-3495(78)85495-2.

Abstract

We have analyzed the decrease in synthesis of individual size classes of heterogeneous nuclear RNA (hnRNA) in ultraviolet (UV)-irradiated Merwin plasmacytoma (MPC-11) cells at various times of postirradiation incubation. HnRNA from nonirradiated control cells is distributed over a wide range from approximately 60S to 5S, with 42S RNA carrying more label than any other size class. HnRNA from UV-irradiated cells shows a dose-dependent shift in size distribution toward lower molecular weight. The size distribution of hnRNA synthesized after prolonged times of postirradiation incubation is restored toward normal, i.e., synthesis of long RNA molecules increases relative to the synthesis of short ones. Analysis of the total number of hnRNA chains synthesized during a 20-min [(3)H]uridine pulse shows a considerable reduction in their number with increasing UV dose. Murine cell lines are excision-repair-deficient but capable of post replication repair inhibited by caffeine. HnRNA transcripts of cells incubated in its presence were studied. The caffeine, which has no effect on hnRNA size in control cells, inhibits to a considerable extent the restoration of full-length transcripts during postirradiation incubation. The lack of excision repair in MPC-11 was confirmed by the analysis of pyrimidine dimers in trichloracetic acid-insoluble and soluble fractions within 8 h of postirradiation incubation.The size of parental and daughter strand DNA in UV-irradiated cells was correlated with RNA transcript size. The parental DNA in these experiments does not change its size as a consequence of UV exposure and postirradiation incubation. In contrast, daughter DNA strands are short in UV-irradiated cells and they increase in size during postirradiation incubation to reach the size of parental strands after 8 h.

摘要

我们分析了紫外线(UV)照射后的默温氏浆细胞瘤(MPC - 11)细胞在照射后不同孵育时间内异质核RNA(hnRNA)各大小类别的合成减少情况。未照射的对照细胞中的hnRNA分布范围很广,从约60S到5S,其中42S RNA携带的标记比其他任何大小类别都多。UV照射细胞的hnRNA在大小分布上呈现出剂量依赖性地向较低分子量转移。照射后长时间孵育合成的hnRNA大小分布恢复正常,即长RNA分子的合成相对于短RNA分子的合成增加。对在20分钟[³H]尿苷脉冲期间合成的hnRNA链总数的分析表明,随着UV剂量增加,其数量显著减少。鼠细胞系缺乏切除修复能力,但能够进行受咖啡因抑制的复制后修复。研究了在咖啡因存在下孵育的细胞的hnRNA转录本。咖啡因在对照细胞中对hnRNA大小没有影响,但在很大程度上抑制了照射后孵育期间全长转录本的恢复。通过分析照射后孵育8小时内三氯乙酸不溶性和可溶性部分中的嘧啶二聚体,证实了MPC - 11中缺乏切除修复。UV照射细胞中亲代和子代DNA链的大小与RNA转录本大小相关。在这些实验中,亲代DNA不会因UV暴露和照射后孵育而改变其大小。相反,UV照射细胞中的子代DNA链较短,并且在照射后孵育期间它们的大小增加,8小时后达到亲代链的大小。

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