A novel interpretable deep learning-based computational framework designed synthetic enhancers with broad cross-species activity

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleic Acids Research Pub Date : 2024-10-18 DOI:10.1093/nar/gkae912
Zhaohong Li, Yuanyuan Zhang, Bo Peng, Shenghua Qin, Qian Zhang, Yun Chen, Choulin Chen, Yongzhou Bao, Yuqi Zhu, Yi Hong, Binghua Liu, Qian Liu, Lingna Xu, Xi Chen, Xinhao Ma, Hongyan Wang, Long Xie, Yilong Yao, Biao Deng, Jiaying Li, Baojun De, Yuting Chen, Jing Wang, Tian Li, Ranran Liu, Zhonglin Tang, Junwei Cao, Erwei Zuo, Chugang Mei, Fangjie Zhu, Changwei Shao, Guirong Wang, Tongjun Sun, Ningli Wang, Gang Liu, Jian-Quan Ni, Yuwen Liu
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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.
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基于深度学习的新型可解释计算框架设计出具有广泛跨物种活性的合成增强子
增强子在动态调控时空基因表达和建立细胞特性方面发挥着关键作用,这突出表明了设计具有特定特性的增强子以应用于生物合成工程和基因治疗的重要性。尽管有许多高通量方法促进了全基因组增强子的鉴定,但破译其活性的序列决定因素仍然具有挑战性。在这里,我们提出了 DREAM(DNA cis-Regulatory Elements with controllable Activity design platforM)框架,这是一种基于深度学习的合成增强子设计新方法。DREAM 擅长在大量增强子筛选数据中发现微妙而复杂的模式,实现了最前沿的基于序列的增强子活性预测,并突出了蕴含强增强子活性的关键序列特征。利用 DREAM,我们设计出的增强子比果蝇基因组中最强增强子的效力高出约 3.6 倍。值得注意的是,这些合成的增强子在已经分化超过十亿年的物种中表现出了保守的功能,这表明 DREAM 能够学习高度保守的增强子调控语法。此外,我们还利用 DREAM 设计了沉默子和细胞系特异性增强子,证明了它的多功能性。总之,我们的研究不仅为增强子设计引入了一种可解释的方法,还为其他类型顺式调控元件的设计提供了一个通用框架。
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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