Log in to save to my catalogue

Decoding gene regulation in the fly brain

Decoding gene regulation in the fly brain

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2560486305

Decoding gene regulation in the fly brain

About this item

Full title

Decoding gene regulation in the fly brain

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2021-08

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

The Drosophila brain is a work horse in neuroscience. Single-cell transcriptome analysis, 3D morphological classification, and detailed EM mapping of the connectome have revealed an immense diversity of neuronal and glial cell types that underlie the wide array of functional and behavioral traits in the fruit fly. The identities of these cell types are controlled by still unknown gene regulatory networks (GRNs), involving combinations of transcription factors that bind to genomic enhancers to regulate their target genes. To characterize the GRN for each cell type in the Drosophila brain, we profiled chromatin accessibility of 240,919 single cells spanning nine developmental timepoints, and integrated this data with single-cell transcriptomes. We identify more than 95,000 regulatory regions that are used in different neuronal cell types, of which around 70,000 are linked to specific developmental trajectories, involving neurogenesis, reprogramming and maturation. For 40 cell types, their uniquely accessible regions could be associated with their expressed transcription factors and downstream target genes, through a combination of motif discovery, network inference techniques, and deep learning. We illustrate how these enhancer-GRNs can be used to reveal enhancer architectures leading to a better understanding of neuronal regulatory diversity. Finally, our atlas of regulatory elements can be used to design genetic driver lines for specific cell types at specific timepoints, facilitating the characterization of brain cell types and the manipulation of brain function. Competing Interest Statement The authors have declared no competing interest. Footnotes * http://flybrain.aertslab.org * http://scope.aertslab.org/#/Fly_Brain/ * http://genome.ucsc.edu/cgi-bin/hgTracks?db=dm6&hubUrl=http://ucsctracks.aertslab.org/papers/FlyBra...

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2560486305

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2560486305

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/2021.08.11.454937