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5-氮杂胞苷诱导的DNA去甲基化对中间球海胆幼虫聚酮合酶基因表达的影响

Effects of 5-azacytidine-induced DNA demethylation on polyketide synthase gene expression in larvae of sea urchin Strongylocentrotus intermedius.

作者信息

Tyunin A P, Ageenko N V, Kiselev K V

机构信息

Laboratory of Biotechnology, Institute of Biology and Soil Science, Far Eastern Branch of Russian Academy of Sciences, Stoletija Str. 159, 690022, Vladivostok, Russia.

Laboratory of Cytotechnology, A.V. Zhirmunsky Institute of Marine Biology, Far Eastern Branch of the Russian Academy of Sciences, Palchevsky St. 17, 690041, Vladivostok, Russia.

出版信息

Biotechnol Lett. 2016 Dec;38(12):2035-2041. doi: 10.1007/s10529-016-2191-3. Epub 2016 Aug 26.

Abstract

OBJECTIVE

To investigate the role of cytosine methylation in regulation of polyketide compounds biosynthesis in larvae of Strongylocentrotus intermedius.

RESULTS

Treatment of S. intermedius larvae with 100 and 200 µM 5-azacytidine (5A) as a DNA demethylating agent significantly increased the amounts of spinochrome D and spinochrome E, as the number of pigmented cells per studied larva, in a dose-depended manner. The data on SiPks gene expression showed enhancement in 16- and 67-fold in S. intermedius larvae treated with 100 and 200 µM 5A, respectively, relative to untreated ones. Moreover, the activation of transcription factors SiGcm, SiGatae and SiKrl gene expression involved in regulation of SiPks was observed in S. intermedius larvae upon treatment with 5A, suggesting DNA methylation being powerful regulator of polyketide compounds biosynthesis.

CONCLUSIONS

This is the first study to describe the role of cytosine DNA methylation in the regulation of polyketide compounds biosynthesis in sea urchins. Current study implies a negative control provided by cytosine DNA methylation machinery as a key regulator of polyketide compound biosynthesis.

摘要

目的

研究胞嘧啶甲基化在中间球海胆幼虫聚酮化合物生物合成调控中的作用。

结果

用100和200 μM 5-氮杂胞苷(5A)作为DNA去甲基化剂处理中间球海胆幼虫,显著增加了海胆色素D和海胆色素E的含量,且呈剂量依赖性,即每个研究幼虫中色素细胞的数量增加。关于SiPks基因表达的数据显示,用100和200 μM 5A处理的中间球海胆幼虫相对于未处理的幼虫,基因表达分别增强了16倍和67倍。此外,在用5A处理的中间球海胆幼虫中,观察到参与SiPks调控的转录因子SiGcm、SiGatae和SiKrl基因表达的激活,这表明DNA甲基化是聚酮化合物生物合成的有力调节因子。

结论

这是首次描述胞嘧啶DNA甲基化在海胆聚酮化合物生物合成调控中作用的研究。当前研究表明,胞嘧啶DNA甲基化机制作为聚酮化合物生物合成的关键调节因子提供了负调控。

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