Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Epigenetics Institute, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA 19104, USA; Department of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA 19104, USA.
Mol Cell. 2023 Jul 20;83(14):2449-2463.e13. doi: 10.1016/j.molcel.2023.06.012. Epub 2023 Jul 3.
Transcription factors (TFs) orchestrate the gene expression programs that define each cell's identity. The canonical TF accomplishes this with two domains, one that binds specific DNA sequences and the other that binds protein coactivators or corepressors. We find that at least half of TFs also bind RNA, doing so through a previously unrecognized domain with sequence and functional features analogous to the arginine-rich motif of the HIV transcriptional activator Tat. RNA binding contributes to TF function by promoting the dynamic association between DNA, RNA, and TF on chromatin. TF-RNA interactions are a conserved feature important for vertebrate development and disrupted in disease. We propose that the ability to bind DNA, RNA, and protein is a general property of many TFs and is fundamental to their gene regulatory function.
转录因子 (TFs) 协调基因表达程序,定义每个细胞的身份。经典的 TF 通过两个结构域实现这一点,一个结构域结合特定的 DNA 序列,另一个结构域结合蛋白质共激活因子或核心抑制因子。我们发现,至少有一半的 TFs 还与 RNA 结合,其通过一个以前未被识别的结构域完成,该结构域具有类似于 HIV 转录激活子 Tat 的精氨酸丰富基序的序列和功能特征。RNA 结合通过促进 DNA、RNA 和 TF 在染色质上的动态相互作用来促进 TF 功能。TF-RNA 相互作用是脊椎动物发育的一个保守特征,在疾病中被破坏。我们提出,结合 DNA、RNA 和蛋白质的能力是许多 TFs 的一般特性,是其基因调控功能的基础。