Reduced Cas9 transgene silencing by incorporation of intron sequences

Silencing remains a significant challenge for exogenous gene expression, limiting both the penetrance and expressivity of transgenes. In particular, silencing of Cas9 expression is a major technical limitation for many gene editing and CRISPR screening applications. Here, we demonstrate that including introns in Cas9 expression cassettes significantly reduces silencing across multiple cell lines. Notably, the incorporation of an intron into a CRISPRa construct results in reduced silencing, increased expression levels, and markedly enhanced activation of target genes. We investigate diverse intron sequences and discover that T-rich introns over 2 kb confer the greatest protection against silencing. In addition, we find that introns can work synergistically with chromatin opening elements to further mitigate silencing, suggesting regulatory mechanisms are acting at both the DNA and RNA level to silence exogenous genes. Our work highlights the potential of introns to optimize genetic constructs for enhanced expression and improved cellular engineering requiring constitutive expression of large transgenes.

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Publication Details

Journal
Nature Communications
Published
2025-11-27
DOI
https://doi.org/10.1038/s41467-025-65669-0
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.00

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article

Reduced Cas9 transgene silencing by incorporation of intron sequences

Raeline Valbuena, Laura M. Prolo, Michael C. Bassik, Thien Nguyen et al.
Nature Communications
CRISPR and Genetic Engineering
article

Reduced Cas9 transgene silencing by incorporation of intron sequences

Raeline Valbuena, Laura M. Prolo, Michael C. Bassik, Thien Nguyen, Peter P. Du, Anthony Venida, Nora J. Enright, Marta Seczyńska, César A. Garcia, Paul J. Lehner, Lacramioara Bintu, Kaitlyn Spees, Alun Vaughan-Jackson, Sophia Arana
article en

Abstract

Silencing remains a significant challenge for exogenous gene expression, limiting both the penetrance and expressivity of transgenes. In particular, silencing of Cas9 expression is a major technical limitation for many gene editing and CRISPR screening applications. Here, we demonstrate that including introns in Cas9 expression cassettes significantly reduces silencing across multiple cell lines. Notably, the incorporation of an intron into a CRISPRa construct results in reduced silencing, increased expression levels, and markedly enhanced activation of target genes. We investigate diverse intron sequences and discover that T-rich introns over 2 kb confer the greatest protection against silencing. In addition, we find that introns can work synergistically with chromatin opening elements to further mitigate silencing, suggesting regulatory mechanisms are acting at both the DNA and RNA level to silence exogenous genes. Our work highlights the potential of introns to optimize genetic constructs for enhanced expression and improved cellular engineering requiring constitutive expression of large transgenes.

Nature CommunicationsVol. 16(1)
Lucile Packard Children's Hospital (US), University of Cambridge (GB), Chan Zuckerberg Initiative (United States) (US), Stanford University (US)
Wellcome Trust, National Cancer Institute
Openalex Percentile: Top 67%
CRISPR and Genetic Engineering
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