Iterative assay for transposase-accessible chromatin by sequencing to isolate functionally relevant neuronal subtypes.
Collin B MerrillIris TitosMiguel A PabonAustin B MontgomeryAylin R RodanAdrian RothenfluhPublished in: Science advances (2024)
The Drosophila brain contains tens of thousands of distinct cell types. Thousands of different transgenic lines reproducibly target specific neuron subsets, yet most still express in several cell types. Furthermore, most lines were developed without a priori knowledge of where the transgenes would be expressed. To aid in the development of cell type-specific tools for neuronal identification and manipulation, we developed an iterative assay for transposase-accessible chromatin (ATAC) approach. Open chromatin regions (OCRs) enriched in neurons, compared to whole bodies, drove transgene expression preferentially in subsets of neurons. A second round of ATAC-seq from these specific neuron subsets revealed additional enriched OCR2s that further restricted transgene expression within the chosen neuron subset. This approach allows for continued refinement of transgene expression, and we used it to identify neurons relevant for sleep behavior. Furthermore, this approach is widely applicable to other cell types and to other organisms.
Keyphrases
- single cell
- poor prognosis
- gene expression
- dna damage
- high throughput
- genome wide
- rna seq
- transcription factor
- cell therapy
- spinal cord
- binding protein
- stem cells
- magnetic resonance imaging
- long non coding rna
- physical activity
- cerebral ischemia
- magnetic resonance
- computed tomography
- white matter
- spinal cord injury
- mesenchymal stem cells
- sleep quality
- image quality
- multidrug resistant