Systematic expression profiling of Dpr and DIP genes reveals cell surface codes in Drosophila larval motor and sensory neurons.
Yupu WangMeike Lobb-RabeJames AshleyPurujit ChatterjeeVeera AnandHugo J BellenOguz KancaRobert A CarrilloPublished in: Development (Cambridge, England) (2022)
In complex nervous systems, neurons must identify their correct partners to form synaptic connections. The prevailing model to ensure correct recognition posits that cell-surface proteins (CSPs) in individual neurons act as identification tags. Thus, knowing what cells express which CSPs would provide insights into neural development, synaptic connectivity, and nervous system evolution. Here, we investigated expression of Dpr and DIP genes, two CSP subfamilies belonging to the immunoglobulin superfamily, in Drosophila larval motor neurons (MNs), muscles, glia and sensory neurons (SNs) using a collection of GAL4 driver lines. We found that Dpr genes are more broadly expressed than DIP genes in MNs and SNs, and each examined neuron expresses a unique combination of Dpr and DIP genes. Interestingly, many Dpr and DIP genes are not robustly expressed, but are found instead in gradient and temporal expression patterns. In addition, the unique expression patterns of Dpr and DIP genes revealed three uncharacterized MNs. This study sets the stage for exploring the functions of Dpr and DIP genes in Drosophila MNs and SNs and provides genetic access to subsets of neurons.
Keyphrases
- genome wide
- genome wide identification
- bioinformatics analysis
- cell surface
- spinal cord
- poor prognosis
- dna methylation
- spinal cord injury
- induced apoptosis
- binding protein
- transcription factor
- cell proliferation
- cell death
- high resolution
- mass spectrometry
- hepatitis c virus
- functional connectivity
- endoplasmic reticulum stress
- zika virus
- long non coding rna
- high speed
- peripheral blood
- aedes aegypti