Molecular Biology Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400085, India.
Ann Bot. 2011 Nov;108(7):1235-46. doi: 10.1093/aob/mcr232. Epub 2011 Sep 6.
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.
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.
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 ATPγS, AMP-PNP and ADP abolished the octamer trans-transfer, indicating the requirement of ATP hydrolysis for this activity.
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.
在真核生物中,染色质重塑复合物被证明负责核小体的迁移,从而增加 DNA 与 DNA 结合蛋白的可及性。尽管已经从生物信息学研究和突变体分析中推测出植物中存在这种复合物,但这种复合物的生化存在仍未得到探索。
通过微球菌核酸酶消化小麦核并通过排阻色谱法进行分级,制备组蛋白 H1 耗尽的供体质粒。通过纤维素磷酸离子交换色谱法对核提取物进行部分纯化。使用合成核小体定位序列在没有 ATP 及其类似物的情况下分析组蛋白八聚体转移转移活性。使用液体闪烁计数法测量 ATP 释放的 ATPase 活性。
使用纤维素磷酸从小麦核部分纯化的 ATP 依赖性组蛋白八聚体转移活性显示,在 ATP 依赖性情况下,从 H1 耗尽的小麦天然供体质粒中的八聚体在反式中转移到标记的合成核小体定位序列。它还显示出核小体依赖性 ATPase 活性。用 ATP 类似物,即 ATPγS、AMP-PNP 和 ADP 替代 ATP 会破坏八聚体转移转移,表明该活性需要 ATP 水解。
ATP 依赖性组蛋白八聚体反式转移是染色质重塑复合物的一种公认活性,对于非植物物种的染色质结构动力学是必需的。我们的结果表明,小麦核也具有类似于其他真核生物的典型染色质重塑活性。这是首次从植物中体外报告染色质重塑活性。