Department of Biochemistry and Molecular Biology, University of Valencia, Valencia, Spain.
New Phytol. 2011 Oct;192(2):353-63. doi: 10.1111/j.1469-8137.2011.03818.x. Epub 2011 Jul 25.
Aspects of transcriptional regulation in plants, such as the order in which transcriptional factors and the preinitiation complex are assembled, are obscure because studies carried out under conditions in which native chromatin structure is preserved are still few in comparison with those carried out under other conditions. In vivo chromatin immunoprecipitation (ChIP) experiments were used here to study the regulation of Pisum sativum psp54, which codes for the precursor of a chromatin-associated protein in dry seeds. Antibodies against PsSNF5, a component of the SWI/SNF remodelling complex, and against the transcriptional factor Pisum sativum abscisic acid insensitive 3 (PsABI3) were raised and used for ChIP experiments, which showed that both factors are bound to the psp54 promoter only when the gene is actively expressed during seed maturation and germination. However, RNA polymerase II appeared to be bound to the inactive promoter, which was poised for transcription, before the assembly of factors. Micrococcal nuclease protection assays showed that chromatin conformation at the proximal psp54 promoter changes in shifting from the active to inactive state. The changes in the promoter chromatin of psp54 are discussed. Stalled polymerase is described for the first time at the promoter of a non-heat-shock plant gene.
植物转录调控的各个方面,如转录因子和起始前复合物的组装顺序,仍然不太清楚,因为与其他条件下进行的研究相比,在保持天然染色质结构的条件下进行的研究仍然很少。本文使用体内染色质免疫沉淀(ChIP)实验来研究豌豆 psp54 的调控,它编码一种在干燥种子中与染色质相关的蛋白质前体。针对 SWI/SNF 重塑复合物的组成部分 PsSNF5 和豌豆 ABA 不敏感 3(PsABI3)转录因子的抗体被制备并用于 ChIP 实验,结果表明,只有在种子成熟和萌发过程中基因活跃表达时,这两种因子才结合到 psp54 启动子上。然而,聚合酶 II 似乎在组装因子之前就结合到了处于转录预备状态的非活性启动子上。微球菌核酸酶保护实验表明,在从活跃状态到不活跃状态转变时,近端 psp54 启动子处的染色质构象发生了变化。讨论了 psp54 启动子染色质的变化。在非热休克植物基因的启动子处首次描述了停滞的聚合酶。