FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Reference Report
Open Close
Reference
Citation
Li, Z., Zhang, Y., Peng, B., Qin, S., Zhang, Q., Chen, Y., Chen, C., Bao, Y., Zhu, Y., Hong, Y., Liu, B., Liu, Q., Xu, L., Chen, X., Ma, X., Wang, H., Xie, L., Yao, Y., Deng, B., Li, J., De, B., Chen, Y., Wang, J., Li, T., Liu, R., Tang, Z., Cao, J., Zuo, E., Mei, C., Zhu, F., Shao, C., Wang, G., Sun, T., Wang, N., Liu, G., Ni, J.Q., Liu, Y. (2024). A novel interpretable deep learning-based computational framework designed synthetic enhancers with broad cross-species activity.  Nucleic Acids Res. 52(21): 13447--13468.
FlyBase ID
FBrf0260989
Publication Type
Research paper
Abstract
Enhancers play a critical role in dynamically regulating spatial-temporal gene expression and establishing cell identity, underscoring the significance of designing them with specific properties for applications in biosynthetic engineering and gene therapy. Despite numerous high-throughput methods facilitating genome-wide enhancer identification, deciphering the sequence determinants of their activity remains challenging. Here, we present the DREAM (DNA cis-Regulatory Elements with controllable Activity design platforM) framework, a novel deep learning-based approach for synthetic enhancer design. Proficient in uncovering subtle and intricate patterns within extensive enhancer screening data, DREAM achieves cutting-edge sequence-based enhancer activity prediction and highlights critical sequence features implicating strong enhancer activity. Leveraging DREAM, we have engineered enhancers that surpass the potency of the strongest enhancer within the Drosophila genome by approximately 3.6-fold. Remarkably, these synthetic enhancers exhibited conserved functionality across species that have diverged more than billion years, indicating that DREAM was able to learn highly conserved enhancer regulatory grammar. Additionally, we designed silencers and cell line-specific enhancers using DREAM, demonstrating its versatility. Overall, our study not only introduces an interpretable approach for enhancer design but also lays out a general framework applicable to the design of other types of cis-regulatory elements.
PubMed ID
PubMed Central ID
PMC11602155 (PMC) (EuropePMC)
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nucleic Acids Res.
    Title
    Nucleic Acids Research
    Publication Year
    1974-
    ISBN/ISSN
    0305-1048
    Data From Reference
    Cell Lines (1)