Transcriptional complexity in the insect central complex: single nuclei RNA sequencing of adult brain neurons derived from type 2 neuroblasts

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:bioRxiv (Mar 3, 2025)
मुख्य लेखक: Epiney, Derek
अन्य लेखक: Gonzalo Morales Chaya, Dillon, Noah, Sen-Lin, Lai, Doe, Chris
प्रकाशित:
Cold Spring Harbor Laboratory Press
विषय:
ऑनलाइन पहुंच:Citation/Abstract
Full Text - PDF
Full text outside of ProQuest
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022 |a 2692-8205 
024 7 |a 10.1101/2023.12.10.571022  |2 doi 
035 |a 2900440995 
045 0 |b d20250303 
100 1 |a Epiney, Derek 
245 1 |a Transcriptional complexity in the insect central complex: single nuclei RNA sequencing of adult brain neurons derived from type 2 neuroblasts 
260 |b Cold Spring Harbor Laboratory Press  |c Mar 3, 2025 
513 |a Working Paper 
520 3 |a In both invertebrates such as Drosophila and vertebrates such as mouse or human, the brain contains the most diverse population of cell types of any tissue. It is generally accepted that transcriptional diversity is an early step in generating neuronal and glial diversity, followed by the establishment of a unique gene expression profile that determines morphology, connectivity, and function. In Drosophila, there are two types of neural stem cells, called Type 1 (T1) and Type 2 (T2) neuroblasts. In contrast to T1 neuroblasts, T2 neuroblasts generate intermediate neural progenitors (INPs) that expand the number and diversity of cell types. The diversity of T2-derived neurons contributes a large portion of the central complex (CX), a conserved brain region that plays a role in sensorimotor integration. Recent work has revealed much of the connectome of the CX, but how this connectome is assembled remains unclear. Mapping the transcriptional diversity of neurons derived from T2 neuroblasts is a necessary step in linking transcriptional profile to the assembly of the adult brain. Here we perform single nuclei RNA sequencing of T2 neuroblast-derived adult neurons and glia. We identify clusters containing all known classes of glia, clusters that are male/female enriched, and 161 neuron-specific clusters. We map neurotransmitter and neuropeptide expression and identify unique transcription factor combinatorial codes for each cluster (presumptive neuron subtype). This is a necessary step that directs functional studies to determine whether each transcription factor combinatorial code specifies a distinct neuron type within the CX. We map several columnar neuron subtypes to distinct clusters and identify two neuronal classes (NPF+ and AstA+) that both map to two closely related clusters. Our data support the hypothesis that each transcriptional cluster represents one or a few closely related neuron subtypes.Competing Interest StatementThe authors have declared no competing interest.Footnotes* final version soon to be in press at eLife. Many changes to the text and figures. 
653 |a Neural stem cells 
653 |a Insects 
653 |a Neurons 
653 |a Neuronal-glial interactions 
653 |a Gene expression 
653 |a Sensorimotor integration 
653 |a Neural networks 
653 |a Transcription factors 
653 |a Neuroblasts 
653 |a Drosophila 
700 1 |a Gonzalo Morales Chaya 
700 1 |a Dillon, Noah 
700 1 |a Sen-Lin, Lai 
700 1 |a Doe, Chris 
773 0 |t bioRxiv  |g (Mar 3, 2025) 
786 0 |d ProQuest  |t Biological Science Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/2900440995/abstract/embedded/Q8Z64E4HU3OH5N8U?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/2900440995/fulltextPDF/embedded/Q8Z64E4HU3OH5N8U?source=fedsrch 
856 4 0 |3 Full text outside of ProQuest  |u https://www.biorxiv.org/content/10.1101/2023.12.10.571022v3