期刊
ACS SYNTHETIC BIOLOGY
卷 10, 期 6, 页码 1438-1450出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.1c00050
关键词
biological parts; intrinsic terminator; transcription termination; de novo design; sequence-activity relationship
资金
- International S&T Innovation Cooperation Key Project [2017YFE0129600]
- National Natural Science Foundation of China [21878125]
- Natural Sciences Foundation of Jiangsu [BK20181206]
- Priority Academic Program Development of Jiangsu Higher Education Institutions
- 111 Project [111-2-06]
- First-Class Discipline Program of Light Industry Technology and Engineering [LITE2018-04]
Efficient transcription termination using intrinsic terminators is crucial for cell fitness in bacteria. A data-driven and in silico-assisted (DISA) design framework was established to engineer minimal intrinsic terminators (MITs) using key features identified in natural intrinsic terminators. The MITs showed high termination efficiency in a wide range of bacteria compared to natural intrinsic terminators, and their efficiency could be flexibly tuned by modulating the length of the U-tract.
Efficient transcription termination relying on intrinsic terminators is critical to maintain cell fitness by avoiding unwanted read-through in bacteria. Natural intrinsic terminator (NIT) typically appears in mRNA as a hairpin followed by approximately eight conserved uridines (U-tract) at the 3' terminus. Owing to their simple structure, small size, and protein independence, assorted NITs have been redesigned as robust tools to construct gene circuits. However, most NITs exert functions to adapt to their physiological requirements rather than the demand for building synthetic gene circuits, rendering uncertain working performance when they are constructed intact in synthetic gene circuits. Here, rather than modifying NITs, we established a data-driven and in silico-assisted (DISA) design framework to forward engineer minimal intrinsic terminators (MITs). By comprehensively analyzing 75 natural intrinsic terminators from Bacillus subtilis, we revealed that two pivotal features, the length of the U-tract and the thermodynamics of the terminator hairpin, were involved in the sequence-activity relationship (SAR) of termination efficiency (TE). As per the SAR, we leveraged DISA to fabricate an array of MITs composed of in silico-assisted designed minimal hairpins and fixed U-tracts. Most of these MITs exhibited high TE in diverse Gram-positive and Gram-negative bacteria. In contrast, the TEs of the NITs were highly varied in different hosts. Moreover, TEs of MITs were flexibly tuned over a wide range by modulating the length of the U-tract. Overall, these results demonstrate an efficient framework to forward design functional and broad host-range terminators independent of tedious and iterative screening of mutagenesis libraries of natural terminators.
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