MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
PLoS One. 2013 Apr 4;8(4):e61059. doi: 10.1371/journal.pone.0061059. Print 2013.
G1/S transcriptional regulation in the budding yeast Saccharomyces cerevisiae depends on three main transcriptional components, Swi4, Swi6 and Mbp1. These proteins constitute two transcription factor complexes that regulate over 300 G1/S transcripts, namely SBF (Swi4-Swi6) and MBF (Mbp1-Swi6). SBF and MBF are involved in regulating largely non-overlapping sets of G1/S genes via clearly distinct mechanisms.
METHODOLOGY/PRINCIPAL FINDINGS: Here we establish and confirm protein-protein and protein-DNA interactions using specific polyclonal antisera to whole Swi6 and to the C-terminal domains of related proteins Swi4 and Mbp1. Our data confirm the protein-protein binding specificity of Swi4 and Mbp1 to Swi6 but not to each other, and support the binding specificity of the transcriptional inhibitor Whi5 to SBF and of the corepressor Nrm1 to MBF. We also show the DNA binding preference of Swi4 to the CLN2 promoter and Mbp1 to the RNR1 promoter, while Swi6 binds both promoters. Finally, we establish the binding dynamics of Swi4 and Whi5 to the CLN2 promoter during the cell cycle.
CONCLUSIONS/SIGNIFICANCE: These data confirm the binding specificity of the G1/S transcriptional regulators. Whereas previous observations were made using tagged Swi4, Swi6 and Mbp1, here we use specific polyclonal antisera to reestablish the protein-protein and protein-DNA interactions of these G1/S transcriptional components. Our data also reveal the dynamic changes in promoter binding of Swi4 during the cell cycle, which suggests a possible positive feedback loop involving Swi4.
在酿酒酵母(Saccharomyces cerevisiae)的芽殖过程中,G1/S 转录调控依赖于三个主要的转录因子,Swi4、Swi6 和 Mbp1。这三种蛋白构成了两个转录因子复合物,调节超过 300 个 G1/S 转录本,即 SBF(Swi4-Swi6)和 MBF(Mbp1-Swi6)。SBF 和 MBF 通过明显不同的机制参与调节大量非重叠的 G1/S 基因。
方法/主要发现:本文通过特异性的多克隆抗体制备 Swi6 全长和相关蛋白 Swi4 和 Mbp1 的 C 端结构域,建立并验证了蛋白-蛋白和蛋白-DNA 的相互作用。我们的数据证实了 Swi4 和 Mbp1 与 Swi6 的蛋白结合特异性,但 Swi4 和 Mbp1 之间没有相互作用,支持了转录抑制剂 Whi5 与 SBF 的结合特异性和核心抑制因子 Nrm1 与 MBF 的结合特异性。我们还展示了 Swi4 对 CLN2 启动子和 Mbp1 对 RNR1 启动子的 DNA 结合偏好性,而 Swi6 则可以结合这两个启动子。最后,我们建立了 Swi4 和 Whi5 在细胞周期中与 CLN2 启动子的结合动力学。
结论/意义:这些数据证实了 G1/S 转录调控因子的结合特异性。尽管之前的观察结果是使用标记的 Swi4、Swi6 和 Mbp1 得出的,但本文使用特异性的多克隆抗体制备,重新建立了这些 G1/S 转录因子的蛋白-蛋白和蛋白-DNA 相互作用。我们的数据还揭示了 Swi4 在细胞周期中启动子结合的动态变化,这表明可能存在涉及 Swi4 的正反馈回路。