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Histone octamer trans-transfer: a signature mechanism of ATP-dependent chromatin remodelling unravelled in wheat nuclear extract

机译:组蛋白八聚体反式转移:揭示小麦核提取物中ATP依赖的染色质重塑的标志性机制

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Background and Scope In eukaryotes, chromatin remodelling complexes are shown to be responsible for nucleosome mobility, leading to increased accessibility of DNA for DNA binding proteins. Although the existence of such complexes in plants has been surmised mainly at the genetic level from bioinformatics studies and analysis of mutants, the biochemical existence of such complexes has remained unexplored.Methods Histone H1-depleted donor chromatin was prepared by micrococcal nuclease digestion of wheat nuclei and fractionation by exclusion chromatography. Nuclear extract was partially purified by cellulose phosphate ion exchange chromatography. Histone octamer trans-transfer activity was analysed using the synthetic nucleosome positioning sequence in the absence and presence of ATP and its analogues. ATPase activity was measured as (32)Pi released using liquid scintillation counting.Key Results ATP-dependent histone octamer trans-transfer activity, partially purified from wheat nuclei using cellulose phosphate, showed ATP-dependent octamer displacement in trans from the H1- depleted native donor chromatin of wheat to the labelled synthetic nucleosome positioning sequence. It also showed nucleosome-dependent ATPase activity. Substitution of ATP by ATP analogues, namely ATP gamma S, AMP-PNP and ADP abolished the octamer trans-transfer, indicating the requirement of ATP hydrolysis for this activity.Conclusions ATP-dependent histone octamer transfer in trans is a recognized activity of chromatin remodelling complexes required for chromatin structure dynamics in non-plant species. Our results suggested that wheat nuclei also possess a typical chromatin remodelling activity, similar to that in other eukaryotes. This is the first report on chromatin remodelling activity in vitro from plants.
机译:背景和范围在真核生物中,染色质重塑复合物被证明是核小体迁移的原因,导致DNA与DNA结合蛋白的可及性增加。尽管从生物信息学研究和突变体分析中主要从遗传水平上推测了植物中此类复合物的存在,但仍未探索此类复合物的生化存在。方法通过微球菌核酸酶消化小麦核,制备了组蛋白H1耗尽的供体染色质。并通过排阻色谱分离。核提取物通过磷酸纤维素离子交换色谱法部分纯化。使用和不存在ATP及其类似物时,使用合成核小体定位序列分析组蛋白八聚体的反式转移活性。 ATP酶活度通过液体闪烁计数测量为(32)Pi释放。关键结果依赖于ATP的组蛋白八聚体反式转移活性(使用磷酸纤维素从小麦核中部分纯化)表明,依赖于ATP的八聚体从耗尽H1的天然蛋白质中转化而来小麦供体染色质与标记的合成核小体定位序列的关系。它还显示了核小体依赖性ATPase活性。 ATP类似物,即ATPγS,AMP-PNP和ADP取代ATP,废除了八聚体的反式转移,表明该活性需要ATP水解。结论ATP依赖的组蛋白八聚体反式转移是染色质重塑的公认活性。非植物物种中染色质结构动力学所需的复合物。我们的结果表明,小麦核还具有典型的染色质重塑活性,与其他真核生物相似。这是关于植物体外染色质重塑活性的首次报道。

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