Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Mol Cell. 2024 Oct 3;84(19):3627-3643. doi: 10.1016/j.molcel.2024.08.021.
Foundational models of transcriptional regulation involve the assembly of protein complexes at DNA elements associated with specific genes. These assemblies, which can include transcription factors, cofactors, RNA polymerase, and various chromatin regulators, form dynamic spatial compartments that contribute to both gene regulation and local genome architecture. This DNA-protein-centric view has been modified with recent evidence that RNA molecules have important roles to play in gene regulation and genome structure. Here, we discuss evidence that gene regulation by RNA occurs at multiple levels that include assembly of transcriptional complexes and genome compartments, feedback regulation of active genes, silencing of genes, and control of protein kinases. We thus provide an RNA-centric view of transcriptional regulation that must reside alongside the more traditional DNA-protein-centric perspectives on gene regulation and genome architecture.
转录调控的基础模型涉及与特定基因相关的 DNA 元件处的蛋白质复合物的组装。这些组装体可以包括转录因子、辅助因子、RNA 聚合酶和各种染色质调节剂,它们形成动态的空间隔室,有助于基因调控和局部基因组结构。随着最近的证据表明 RNA 分子在基因调控和基因组结构中具有重要作用,这种以 DNA-蛋白为中心的观点已经得到了修正。在这里,我们讨论了 RNA 参与基因调控的证据,这些证据发生在多个层面,包括转录复合物和基因组隔室的组装、活性基因的反馈调节、基因沉默以及蛋白激酶的控制。因此,我们提供了一种以 RNA 为中心的转录调控观点,该观点必须与基因调控和基因组结构的更传统的 DNA-蛋白为中心的观点并存。