Author
Listed:
- Jasper Janssens
(VIB Center for Brain & Disease Research
KU Leuven)
- Sara Aibar
(VIB Center for Brain & Disease Research
KU Leuven)
- Ibrahim Ihsan Taskiran
(VIB Center for Brain & Disease Research
KU Leuven)
- Joy N. Ismail
(VIB Center for Brain & Disease Research
KU Leuven)
- Alicia Estacio Gomez
(Imperial College London)
- Gabriel Aughey
(Imperial College London)
- Katina I. Spanier
(VIB Center for Brain & Disease Research
KU Leuven)
- Florian V. Rop
(VIB Center for Brain & Disease Research
KU Leuven)
- Carmen Bravo González-Blas
(VIB Center for Brain & Disease Research
KU Leuven)
- Marc Dionne
(Imperial College London)
- Krista Grimes
(Imperial College London)
- Xiao Jiang Quan
(VIB Center for Brain & Disease Research
KU Leuven)
- Dafni Papasokrati
(VIB Center for Brain & Disease Research
KU Leuven)
- Gert Hulselmans
(VIB Center for Brain & Disease Research
KU Leuven)
- Samira Makhzami
(VIB Center for Brain & Disease Research
KU Leuven)
- Maxime Waegeneer
(VIB Center for Brain & Disease Research
KU Leuven)
- Valerie Christiaens
(VIB Center for Brain & Disease Research
KU Leuven)
- Tony Southall
(Imperial College London)
- Stein Aerts
(VIB Center for Brain & Disease Research
KU Leuven)
Abstract
The Drosophila brain is a frequently used model in neuroscience. Single-cell transcriptome analysis1–6, three-dimensional morphological classification7 and electron microscopy mapping of the connectome8,9 have revealed an immense diversity of neuronal and glial cell types that underlie an array of functional and behavioural traits in the fly. The identities of these cell types are controlled by gene regulatory networks (GRNs), involving combinations of transcription factors that bind to genomic enhancers to regulate their target genes. Here, to characterize GRNs at the cell-type level in the fly brain, we profiled the chromatin accessibility of 240,919 single cells spanning 9 developmental timepoints and integrated these data with single-cell transcriptomes. We identify more than 95,000 regulatory regions that are used in different neuronal cell types, of which 70,000 are linked to developmental trajectories involving neurogenesis, reprogramming and maturation. For 40 cell types, uniquely accessible regions were associated with their expressed transcription factors and downstream target genes through a combination of motif discovery, network inference and deep learning, creating enhancer GRNs. The enhancer architectures revealed by DeepFlyBrain lead to a better understanding of neuronal regulatory diversity and can be used to design genetic driver lines for cell types at specific timepoints, facilitating their characterization and manipulation.
Suggested Citation
Jasper Janssens & Sara Aibar & Ibrahim Ihsan Taskiran & Joy N. Ismail & Alicia Estacio Gomez & Gabriel Aughey & Katina I. Spanier & Florian V. Rop & Carmen Bravo González-Blas & Marc Dionne & Krista G, 2022.
"Decoding gene regulation in the fly brain,"
Nature, Nature, vol. 601(7894), pages 630-636, January.
Handle:
RePEc:nat:nature:v:601:y:2022:i:7894:d:10.1038_s41586-021-04262-z
DOI: 10.1038/s41586-021-04262-z
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