دورية أكاديمية

Multiple Alternative Promoters and Alternative Splicing Enable Universal Transcription-Based Logic Computation in Mammalian Cells

التفاصيل البيبلوغرافية
العنوان: Multiple Alternative Promoters and Alternative Splicing Enable Universal Transcription-Based Logic Computation in Mammalian Cells
المؤلفون: Jiten Doshi, Katie Willis, Angela Madurga, Christoph Stelzer, Yaakov Benenson
المصدر: Cell Reports, Vol 33, Iss 9, Pp 108437- (2020)
بيانات النشر: Elsevier, 2020.
سنة النشر: 2020
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: biomolecular computing, alternative splicing, DNF logic, mammalian cells, gene circuits, synthetic biology, Biology (General), QH301-705.5
الوصف: Summary: Multi-input logic gene circuits can enable sophisticated control of cell function, yet large-scale synthetic circuitry in mammalian cells has relied on post-transcriptional regulation or recombinase-triggered state transitions. Large-scale transcriptional logic, on the other hand, has been challenging to implement. Inspired by a naturally found regulatory strategy of using multiple alternative promoters, followed by alternative splicing, we developed a scalable and compact platform for transcriptional OR logic using inputs to those promoters. The platform is extended to implement disjunctive normal form (DNF) computations capable of implementing arbitrary logic rules. Specifically, AND logic is implemented at individual promoters using synergistic transcriptional inputs, and NOT logic via microRNA inputs targeting unique exon sequences driven by those promoters. Together, these regulatory programs result in DNF-like logic control of output gene expression. The approach offers flexibility for building complex logic programs in mammalian cells.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2211-1247
العلاقة: http://www.sciencedirect.com/science/article/pii/S2211124720314261Test; https://doaj.org/toc/2211-1247Test
DOI: 10.1016/j.celrep.2020.108437
الوصول الحر: https://doaj.org/article/1c1ecda421324a288cda07be3cebf015Test
رقم الانضمام: edsdoj.1c1ecda421324a288cda07be3cebf015
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22111247
DOI:10.1016/j.celrep.2020.108437