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Updated: Sep 24, 2026

Massively Parallel Reporter Assays in Cultured Mammalian Cells
Published on: August 17, 2014
Designing gene expression with MPRA and AI: A new paradigm for synthetic and therapeutic regulation
Xue Zhang1, Xiao-Yan Huang2, Hui-Yu Wang3
1Zhejiang Key Laboratory of Multiomics and Molecular Enzymology, Yangtze Delta Region Institute of Tsinghua University, Zhejiang 314006, China; Department of Biotechnology and Biomedicine, Yangtze Delta Region Institute of Tsinghua University, Zhejiang 314006, China.
Abstract:
Precise and scalable control of gene expression across biological contexts remains a fundamental challenge in synthetic biology and therapeutic development, and massively parallel reporter assays (MPRAs) have emerged as a transformative platform for systematically interrogating cis-regulatory elements (CREs) and enabling high-throughput and quantitative dissection of sequence-dependent transcriptional activity to address this challenge. Beyond their original role in empirical characterization, the convergence of barcoded MPRA technologies with deep learning-based modeling has substantially expanded their impact, facilitating predictive inference and the de novo design of synthetic regulatory elements with programmable behavior. In this review, we synthesize recent advances in barcoded MPRA platforms and AI-driven modeling frameworks for the rational engineering of CREs with tunable transcriptional strength and specificity. We further highlight cutting-edge applications in microbial synthetic biology, mRNA therapeutics, and cell-specific gene regulation, emphasizing the role of barcoded MPRA in supporting data-efficient and cross-context generalizable design. Finally, we discuss current technical and conceptual limitations and future directions toward safe, programmable, and clinically relevant regulatory control systems, outlining a roadmap for next-generation cis-regulatory engineering and gene therapies.
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