4.8 Article

Using Targeted Chromatin Regulators to Engineer Combinatorial and Spatial Transcriptional Regulation

期刊

CELL
卷 158, 期 1, 页码 110-120

出版社

CELL PRESS
DOI: 10.1016/j.cell.2014.04.047

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资金

  1. NIH-NIGMS Ruth L. Kirschstein Postdoctoral Fellowship [1F32GM105272-01A1]
  2. Boehringer Ingelheim Fonds PhD Fellowship
  3. Defense Advanced Research Projects Agency [DARPA-BAA-11-23]
  4. startup funds from the Department of Biomedical Engineering at Boston University
  5. National Science Foundation CAREER Award [MCB-1350949]
  6. Wyss Institute for Biologically Inspired Engineering [PRJ-0329]
  7. Howard Hughes Medical Institute
  8. Direct For Biological Sciences
  9. Div Of Molecular and Cellular Bioscience [1350949] Funding Source: National Science Foundation

向作者/读者索取更多资源

The transcription of genomic information in eukaryotes is regulated in large part by chromatin. How a diverse array of chromatin regulator (CR) proteins with different functions and genomic localization patterns coordinates chromatin activity to control transcription remains unclear. Here, we take a synthetic biology approach to decipher the complexity of chromatin regulation by studying emergent transcriptional behaviors from engineered combinatorial, spatial, and temporal patterns of individual CRs. We fuse 223 yeast CRs to programmable zinc finger proteins. Site-specific and combinatorial recruitment of CRs to distinct intralocus locations reveals a range of transcriptional logic and behaviors, including synergistic activation, long-range and spatial regulation, and gene expression memory. Comparing these transcriptional behaviors with annotated CR complex and function terms provides design principles for the engineering of transcriptional regulation. This work presents a bottom-up approach to investigating chromatin-mediated transcriptional regulation and introduces chromatin-based components and systems for synthetic biology and cellular engineering.

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