| Autor: |
de Almeida, Bernardo P., Schaub, Christoph, Pagani, Michaela, Secchia, Stefano, Furlong, Eileen E. M., Stark, Alexander |
| Zdroj: |
Nature; Feb2024, Vol. 626 Issue 7997, p207-211, 5p |
| Abstrakt: |
Enhancers control gene expression and have crucial roles in development and homeostasis1–3. However, the targeted de novo design of enhancers with tissue-specific activities has remained challenging. Here we combine deep learning and transfer learning to design tissue-specific enhancers for five tissues in the Drosophila melanogaster embryo: the central nervous system, epidermis, gut, muscle and brain. We first train convolutional neural networks using genome-wide single-cell assay for transposase-accessible chromatin with sequencing (ATAC-seq) datasets and then fine-tune the convolutional neural networks with smaller-scale data from in vivo enhancer activity assays, yielding models with 13% to 76% positive predictive value according to cross-validation. We designed and experimentally assessed 40 synthetic enhancers (8 per tissue) in vivo, of which 31 (78%) were active and 27 (68%) functioned in the target tissue (100% for central nervous system and muscle). The strategy of combining genome-wide and small-scale functional datasets by transfer learning is generally applicable and should enable the design of tissue-, cell type- and cell state-specific enhancers in any system.Deep learning and transfer learning were used to design tissue-specific enhancers in the Drosophila embryo that were active and specific, validating this approach to achieve tissue-, cell type- and cell state-specific expression control. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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