Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
J Mol Biol. 2021 Jul 9;433(14):166883. doi: 10.1016/j.jmb.2021.166883. Epub 2021 Feb 20.
Although we have made significant progress, we still possess a limited understanding of how genomic and epigenomic information directs gene expression programs through sequence-specific transcription factors (TFs). Extensive research has settled on three general classes of TF targets in metazoans: promoter accessibility via chromatin regulation (e.g., SAGA), assembly of the general transcription factors on promoter DNA (e.g., TFIID), and recruitment of RNA polymerase (Pol) II (e.g., Mediator) to establish a transcription pre-initiation complex (PIC). Here we discuss TFs and their targets. We also place this in the context of our current work with Saccharomyces (yeast), where we find that promoters typically lack an architecture that supports TF function. Moreover, yeast promoters that support TF binding also display interactions with cofactors like SAGA and Mediator, but not TFIID. It is unknown to what extent all genes in metazoans require TFs and their cofactors.
尽管我们已经取得了重大进展,但对于基因组和表观基因组信息如何通过序列特异性转录因子 (TF) 指导基因表达程序,我们的理解仍然有限。大量研究确定了后生动物中三类一般的 TF 靶标:通过染色质调节获得启动子可及性(例如 SAGA),在启动子 DNA 上组装一般转录因子(例如 TFIID),以及招募 RNA 聚合酶 (Pol) II(例如 Mediator)以建立转录起始前复合物 (PIC)。在这里,我们讨论 TF 和它们的靶标。我们还将其置于我们目前在酿酒酵母 (yeast) 中的工作背景下,我们发现启动子通常缺乏支持 TF 功能的结构。此外,支持 TF 结合的酵母启动子也与 SAGA 和 Mediator 等辅助因子相互作用,但不与 TFIID 相互作用。目前还不清楚后生动物中的所有基因在多大程度上都需要 TF 和它们的辅助因子。