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Programmable mutually exclusive alternative splicing for generating RNA and protein diversity

Author

Listed:
  • Melina Mathur

    (Stanford University)

  • Cameron M. Kim

    (Stanford University)

  • Sarah A. Munro

    (Stanford University
    Joint Initiative for Metrology in Biology
    National Institute of Standards and Technology
    University of Minnesota)

  • Shireen S. Rudina

    (Stanford University)

  • Eric M. Sawyer

    (Stanford University
    University of California, Berkeley)

  • Christina D. Smolke

    (Stanford University
    Chan Zuckerberg Biohub)

Abstract

Alternative splicing performs a central role in expanding genomic coding capacity and proteomic diversity. However, programming of splicing patterns in engineered biological systems remains underused. Synthetic approaches thus far have predominantly focused on controlling expression of a single protein through alternative splicing. Here, we describe a modular and extensible platform for regulating four programmable exons that undergo a mutually exclusive alternative splicing event to generate multiple functionally-distinct proteins. We present an intron framework that enforces the mutual exclusivity of two internal exons and demonstrate a graded series of consensus sequence elements of varying strengths that set the ratio of two mutually exclusive isoforms. We apply this framework to program the DNA-binding domains of modular transcription factors to differentially control downstream gene activation. This splicing platform advances an approach for generating diverse isoforms and can ultimately be applied to program modular proteins and increase coding capacity of synthetic biological systems.

Suggested Citation

  • Melina Mathur & Cameron M. Kim & Sarah A. Munro & Shireen S. Rudina & Eric M. Sawyer & Christina D. Smolke, 2019. "Programmable mutually exclusive alternative splicing for generating RNA and protein diversity," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10403-w
    DOI: 10.1038/s41467-019-10403-w
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    Cited by:

    1. Jonathan P. Ling & Alexei M. Bygrave & Clayton P. Santiago & Rogger P. Carmen-Orozco & Vickie T. Trinh & Minzhong Yu & Yini Li & Ying Liu & Kyra D. Bowden & Leighton H. Duncan & Jeong Han & Kamil Tane, 2022. "Cell-specific regulation of gene expression using splicing-dependent frameshifting," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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