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| Status |
Public on Jan 01, 2022 |
| Title |
A comprehensive series of temporal transcription factors in the fly visual system |
| Organism |
Drosophila melanogaster |
| Experiment type |
Expression profiling by high throughput sequencing
|
| Summary |
The brain consists of hundreds or thousands of different neuronal types that are generated through multiple divisions of neuronal stem cells. These stem cells have the capacity to generate different neuronal types at different stages of their development. In Drosophila, this temporal patterning is driven by the successive expression of temporal transcription factors (tTFs). While a number of tTFs are known in different animals and across various parts of the nervous system, these have been mostly identified by informed guesses and antibody availability. We used single-cell mRNA sequencing to identify the likely complete series of tTFs that specify most Drosophila medulla neurons in the optic lobe. We tested the genetic interactions among these tTFs. While we verify the general principle that tTFs regulate the progression of the series by activating the next tTFs in the series and repressing the previous ones, we also identify more complex regulations. Two of the tTFs, Eyeless and Dichaete, act as hubs integrating the input of several upstream tTFs before allowing the series to progress and in turn regulating the expression of several tTFs. Moreover, we show that tTFs not only specify neuronal identity but also control subsequent neuronal differentiation. We find that terminal differentiation genes, such as neurotransmitter-related genes, are present as transcripts, but not as proteins, in immature larval neurons days before they are being used in functioning neurons; we show that these mechanisms are conserved in humans. Our results offer a comprehensive description of a temporal series of tTFs in a neuronal system, offering mechanistic insights into the regulation of the progression of the series and the regulation of neuronal diversity. This represents a proof-of-principle for the use of single-cell mRNA sequencing for the comparison of temporal patterning across phyla that can lead to an understanding of how the human brain develops and how it has evolved.
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| Overall design |
49,893 single-cell transcriptomes from 40 L3 optic lobes were analyzed using 10XGenomics single-cell sequencing in 10 different experiments
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| Contributor(s) |
Konstantinides N, Desplan C |
| Citation(s) |
35388222, 37609218 |
| Submission date |
Feb 22, 2021 |
| Last update date |
Sep 14, 2023 |
| Contact name |
NIKOLAOS KONSTANTINIDES |
| E-mail(s) |
nikos.konstantinides@ijm.fr
|
| Organization name |
Institut Jacques Monod
|
| Lab |
Konstantinides
|
| Street address |
15 rue Helene Brion
|
| City |
Paris |
| ZIP/Postal code |
75013 |
| Country |
France |
| |
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| Platforms (1) |
| GPL25244 |
Illumina NovaSeq 6000 (Drosophila melanogaster) |
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| Samples (10)
|
| GSM5100583 |
wild type third instar larval optic lobe rep 1 |
| GSM5100584 |
wild type third instar larval optic lobe rep 2 |
| GSM5100585 |
wild type third instar larval optic lobe rep 3 |
| GSM5100586 |
wild type third instar larval optic lobe rep 4 |
| GSM5100587 |
wild type third instar larval optic lobe rep 5 |
| GSM5100588 |
wild type third instar larval optic lobe rep 6 |
| GSM5100589 |
wild type third instar larval optic lobe rep 7 |
| GSM5100590 |
wild type third instar larval optic lobe rep 8 |
| GSM5100591 |
wild type third instar larval optic lobe rep 9 |
| GSM5100592 |
wild type third instar larval optic lobe rep 10 |
|
| Relations |
| BioProject |
PRJNA704024 |
| SRA |
SRP307551 |
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