4.4 Article

Dynamic transcription regulation at the single-molecule level

Journal

DEVELOPMENTAL BIOLOGY
Volume 482, Issue -, Pages 67-81

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2021.11.004

Keywords

Single-molecule imaging; RNA polymerase II; Transcription factor; Chromatin regulation

Funding

  1. Beijing Advanced Innovation Center for Genomics (ICG) at Peking University
  2. Peking-Tsinghua Center for Life Sciences (CLS)
  3. National Key R&D Program of China [2020YFA0509502]
  4. National Natural Science Foundation of China [32170566]

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This review focuses on the single-molecule dynamic features of transcription regulatory events observed in living cells using live-cell single-molecule imaging techniques, and discusses their biological relevance and interpretation in understanding the mechanisms of transcription regulation.
Cell fate changes during development, differentiation, and reprogramming are largely controlled at the transcription level. The DNA-binding transcription factors (TFs) often act in a combinatorial fashion to alter chromatin states and drive cell type-specific gene expression. Recent advances in fluorescent microscopy technologies have enabled direct visualization of biomolecules involved in the process of transcription and its regulatory events at the single-molecule level in living cells. Remarkably, imaging and tracking individual TF molecules at high temporal and spatial resolution revealed that they are highly dynamic in searching and binding cognate targets, rather than static and binding constantly. In combination with investigation using techniques from biochemistry, structure biology, genetics, and genomics, a more well-rounded view of transcription regulation is emerging. In this review, we briefly cover the technical aspects of live-cell single-molecule imaging and focus on the biological relevance and interpretation of the single-molecule dynamic features of transcription regulatory events observed in the native chromatin environment of living eukaryotic cells. We also discuss how these dynamic features might shed light on mechanistic understanding of transcription regulation.

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