| Literature DB >> 26092715 |
Caroline Bivik1, Shahrzad Bahrampour1, Carina Ulvklo1, Patrik Nilsson1, Anna Angel1, Fredrik Fransson1, Erika Lundin1, Jakob Renhorn1, Stefan Thor2.
Abstract
The expression of neuropeptides is often extremely restricted in the nervous system, making them powerful markers for addressing cell specification . In the developing Drosophila ventral nerve cord, only six cells, the Ap4 neurons, of some 10,000 neurons, express the neuropeptide FMRFamide (FMRFa). Each Ap4/FMRFa neuron is the last-born cell generated by an identifiable and well-studied progenitor cell, neuroblast 5-6 (NB5-6T). The restricted expression of FMRFa and the wealth of information regarding its gene regulation and Ap4 neuron specification makes FMRFa a valuable readout for addressing many aspects of neural development, i.e., spatial and temporal patterning cues, cell cycle control, cell specification, axon transport, and retrograde signaling. To this end, we have conducted a forward genetic screen utilizing an Ap4-specific FMRFa-eGFP transgenic reporter as our readout. A total of 9781 EMS-mutated chromosomes were screened for perturbations in FMRFa-eGFP expression, and 611 mutants were identified. Seventy-nine of the strongest mutants were mapped down to the affected gene by deficiency mapping or whole-genome sequencing. We isolated novel alleles for previously known FMRFa regulators, confirming the validity of the screen. In addition, we identified novel essential genes, including several with previously undefined functions in neural development. Our identification of genes affecting most major steps required for successful terminal differentiation of Ap4 neurons provides a comprehensive view of the genetic flow controlling the generation of highly unique neuronal cell types in the developing nervous system.Entities:
Keywords: CNS development; Drosophila; FMRFamide; forward genetic screening; neural cell fate specification
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Year: 2015 PMID: 26092715 PMCID: PMC4574234 DOI: 10.1534/genetics.115.178483
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562