A toolkit for programmable transcriptional engineering across eukaryotic kingdoms

Chromatin is essential for eukaryotic life. Tens of thousands of chromatin regulator (CR) proteins exist in eukaryotic genomes that are predicted to modulate chromatin states; however, their molecular functions remain largely untested experimentally. Here, we construct a library of over 300 full-length CRs from humans, plants, yeast, protozoa, and virus, each fused to DNA-binding domains, and test their direct effect on transcriptional repression and activation in plants and human cells. We discover CRs with cross-kingdom functionality when transferred across eukaryotes, including CRs that outperform existing tools for programmable transcriptional repression and activation in plants and human cells. Using pooled CRISPR screens, we demonstrate a suite of CRISPR repressors that titrate gene expression at intermediate levels. Finally, we identify RCOR1 and MTA2 as universal eukaryotic repressors that retain repressive activity in plants, yeast, and human cells. Our toolkit advances synthetic eukaryotic engineering and expands our understanding of CR functionality across eukaryotes.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-11
DOI
https://doi.org/10.64898/2026.02.10.705154
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

A toolkit for programmable transcriptional engineering across eukaryotic kingdoms

Izaiah J. Ornelas, Niklas F. C. Hummel, Rithu Pattali, Lauren A. Owens et al.
bioRxiv (Cold Spring Harbor Laboratory)
Genomics and Chromatin Dynamics
article

A toolkit for programmable transcriptional engineering across eukaryotic kingdoms

Izaiah J. Ornelas, Niklas F. C. Hummel, Rithu Pattali, Lauren A. Owens, Simón Álamos, James K. Nuñez, Martin R. Zamora, Patrick M Shih, Ngan T Phan
article en

Abstract

Chromatin is essential for eukaryotic life. Tens of thousands of chromatin regulator (CR) proteins exist in eukaryotic genomes that are predicted to modulate chromatin states; however, their molecular functions remain largely untested experimentally. Here, we construct a library of over 300 full-length CRs from humans, plants, yeast, protozoa, and virus, each fused to DNA-binding domains, and test their direct effect on transcriptional repression and activation in plants and human cells. We discover CRs with cross-kingdom functionality when transferred across eukaryotes, including CRs that outperform existing tools for programmable transcriptional repression and activation in plants and human cells. Using pooled CRISPR screens, we demonstrate a suite of CRISPR repressors that titrate gene expression at intermediate levels. Finally, we identify RCOR1 and MTA2 as universal eukaryotic repressors that retain repressive activity in plants, yeast, and human cells. Our toolkit advances synthetic eukaryotic engineering and expands our understanding of CR functionality across eukaryotes.

bioRxiv (Cold Spring Harbor Laboratory)
Lawrence Berkeley National Laboratory (US), Chan Zuckerberg Biohub San Francisco (US), Innovative Genomics Institute (US), Joint BioEnergy Institute (US), University of California, Berkeley (US)
National Science Foundation, U.S. Department of Energy, Cancer Research Coordinating Committee, Joint Genome Institute, National Institutes of Health, Office of Science, University of California, San Francisco, Biological and Environmental Research, Lawrence Berkeley National Laboratory
Openalex Percentile: Top 59%
Genomics and Chromatin Dynamics
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