Center for Integrative Genomics Faculty of Biology and Medicine University of Lausanne, Lausanne, Switzerland.
Department of Ecology and Evolution Faculty of Biology and Medicine University of Lausanne, Lausanne, Switzerland.
Elife. 2021 Mar 5;10:e63036. doi: 10.7554/eLife.63036.
Determining the molecular properties of neurons is essential to understand their development, function and evolution. Using Targeted DamID (TaDa), we characterize RNA polymerase II occupancy and chromatin accessibility in selected ()-expressing olfactory sensory neurons in . Although individual populations represent a minute fraction of cells, TaDa is sufficiently sensitive and specific to identify the expected receptor genes. Unique expression is not consistently associated with differences in chromatin accessibility, but rather to distinct transcription factor profiles. Genes that are heterogeneously expressed across populations are enriched for neurodevelopmental factors, and we identify functions for the POU-domain protein Pdm3 as a genetic switch of Ir neuron fate, and the atypical cadherin Flamingo in segregation of neurons into discrete glomeruli. Together this study reveals the effectiveness of TaDa in profiling rare neural populations, identifies new roles for a transcription factor and a neuronal guidance molecule, and provides valuable datasets for future exploration.
确定神经元的分子特性对于理解它们的发育、功能和进化至关重要。利用靶向 DamID(TaDa),我们在 中对表达 () 的选定嗅觉感觉神经元中的 RNA 聚合酶 II 占据和染色质可及性进行了表征。尽管各个群体仅代表细胞的一小部分,但 TaDa 足够灵敏和特异,能够识别预期的受体基因。独特的表达并不总是与染色质可及性的差异相关,而是与不同的转录因子谱相关。在群体中异质表达的基因富含神经发育因子,我们确定了 POU 结构域蛋白 Pdm3 作为 Ir 神经元命运的遗传开关的功能,以及非典型钙粘蛋白 Flamingo 在神经元分离成离散的神经小球中的作用。这项研究共同揭示了 TaDa 对稀有神经群体进行分析的有效性,为一个转录因子和一个神经元导向分子确定了新的作用,并为未来的探索提供了有价值的数据集。