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Novel Genes Involved in Controlling Specification of Drosophila FMRFamide Neuropeptide Cells

Bivik, Caroline (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Medicinska fakulteten
Bahrampour, Shahrzad (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Medicinska fakulteten
Ulvklo, Carina (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Medicinska fakulteten
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Nilsson, Patrik (author)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Medicinska fakulteten
Angel, Anna (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Medicinska fakulteten
Fransson, Fredrik (author)
Linköpings universitet,Medicinska fakulteten,Avdelningen för mikrobiologi och molekylär medicin
Lundin, Erika (author)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Medicinska fakulteten
Renhorn, Jakob (author)
Linköpings universitet,Avdelningen för cellbiologi,Medicinska fakulteten
Thor, Stefan (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Medicinska fakulteten
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 (creator_code:org_t)
2015-06-18
2015
English.
In: Genetics. - : Genetics Society of America. - 0016-6731 .- 1943-2631. ; 200:4, s. 1229-1244
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

Drosophila; CNS development; neural cell fate specification; forward genetic screening; FMRFamide

Publication and Content Type

ref (subject category)
art (subject category)

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