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   <dc:title>A targeted genetic screen identifies crucial players in the specification of the Drosophila abdominal Capaergic neurons</dc:title>
   <dc:creator>Gabilondo, Hugo </dc:creator>
   <dc:creator>Losada Pérez, María De La Paloma</dc:creator>
   <dc:creator>del Saz, Delia </dc:creator>
   <dc:creator>Molina, Isabel </dc:creator>
   <dc:creator>León, Yolanda </dc:creator>
   <dc:creator>Canal, Inmaculada </dc:creator>
   <dc:creator>Torroja, Laura </dc:creator>
   <dc:creator>Benito-Sipos, Jonathan</dc:creator>
   <dc:subject>612.82</dc:subject>
   <dc:subject>Neurociencias (Biológicas)</dc:subject>
   <dc:subject>2409.02 Ingeniería Genética</dc:subject>
   <dc:description>This work was supported by a grant from the Spanish Ministerio de Ciencia e Innovación (BFU-2008-04683-C02-02 to L.T.).</dc:description>
   <dc:description>The central nervous system contains a wide variety of neuronal subclasses generated by neural progenitors. The achievement of a unique neural fate is the consequence of a sequence of early and increasingly restricted regulatory events, which culminates in the expression of a specific genetic combinatorial code that confers individual characteristics to the differentiated cell. How the earlier regulatory events influence post-mitotic cell fate decisions is beginning to be understood in the Drosophila NB 5-6 lineage. However, it remains unknown to what extent these events operate in other lineages. To better understand this issue, we have used a very highly specific marker that identifies a small subset of abdominal cells expressing the Drosophila neuropeptide Capa: the ABCA neurons. Our data support the birth of the ABCA neurons from NB 5-3 in a cas temporal window in the abdominal segments A2–A4. Moreover, we show that the ABCA neuron has an ABCA-sibling cell which dies by apoptosis. Surprisingly, both cells are also generated in the abdominal segments A5–A7, although they undergo apoptosis before expressing Capa. In addition, we have performed a targeted genetic screen to identify players involved in ABCA specification. We have found that the ABCA fate requires zfh2, grain, Grunge and hedgehog genes. Finally, we show that the NB 5-3 generates other subtype of Capa-expressing cells (SECAs) in the third suboesophageal segment, which are born during a pdm/cas temporal window, and have different genetic requirements for their specification.</dc:description>
   <dc:description>Ministerio de Ciencia e Innovación (España)</dc:description>
   <dc:description>Depto. de Biología Celular</dc:description>
   <dc:description>Fac. de Ciencias Biológicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-01-23T14:19:27Z</dc:date>
   <dc:date>2024-01-23T14:19:27Z</dc:date>
   <dc:date>2011</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/94807</dc:identifier>
   <dc:identifier>0925-4773</dc:identifier>
   <dc:identifier>10.1016/j.mod.2011.01.002</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>BFU-2008-04683-C02-02</dc:relation>
   <dc:relation>Gabilondo, Hugo, et al. «A Targeted Genetic Screen Identifies Crucial Players in the Specification of the Drosophila Abdominal Capaergic Neurons». Mechanisms of Development, vol. 128, n.o 3-4, marzo de 2011, pp. 208-21. https://doi.org/10.1016/j.mod.2011.01.002.</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
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