Squeeze involvement in the specification of Drosophila leucokinergic neurons: Different regulatory mechanisms endow the same neuropeptide selection

• Published in: Mechanisms of development Vol. 124; no. 6; pp. 427 - 440
• Main Authors: Herrero, Pilar, Magariños, Marta, Molina, Isabel, Benito, Jonathan, Dorado, Belén, Turiégano, Enrique, Canal, Inmaculada, Torroja, Laura
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 01.07.2007
• Subjects: Animals; Axons - metabolism; Drosophila; Drosophila melanogaster - genetics; Drosophila melanogaster - metabolism; Drosophila melanogaster - physiology; Drosophila Proteins - analysis; Drosophila Proteins - genetics; Drosophila Proteins - metabolism; Drosophila Proteins - physiology; Homeodomain Proteins - genetics; Homeodomain Proteins - metabolism; Leucokinergic regulation; Leucokinin; LIM-Homeodomain Proteins; Neurons - metabolism; Neuropeptidergic cell identity; Neuropeptides - analysis; Neuropeptides - metabolism; Neurosecretion - genetics; Squeeze transcription factor; Squeeze–Apterous interaction; Transcription Factors - genetics; Transcription Factors - metabolism; Transcription Factors - physiology; Squeeze–Apterous interaction; Leucokinergic regulation; Neuropeptidergic cell identity; Leucokinin; Squeeze transcription factor; Drosophila
• ISSN: 0925-4773; 1872-6356
• DOI: 10.1016/j.mod.2007.03.001

One of the most widely studied phenomena in the establishment of neuronal identity is the determination of neurosecretory phenotype, in which cell-type-specific combinatorial codes direct distinct neurotransmitter or neuropeptide selection. However, neuronal types from divergent lineages may adopt the same neurosecretory phenotype, and it is unclear whether different classes of neurons use different or similar components to regulate shared features of neuronal identity. We have addressed this question by analyzing how differentiation of the Drosophila larval leucokinergic system, which is comprised of only four types of neurons, is regulated by factors known to affect expression of the FMRFamide neuropeptide. We show that all leucokinergic cells express the transcription factor Squeeze (Sqz). However, based on the effect on LK expression of loss- and gain-of-function mutations, we can describe three types of Lk regulation. In the brain LHLK cells, both Sqz and Apterous (Ap) are required for LK expression, but surprisingly, high levels of either Sqz or Ap alone are sufficient to restore LK expression in these neurons. In the suboesophageal SELK cells, Sqz, but not Ap, is required for LK expression. In the abdominal ABLK neurons, inhibition of retrograde axonal transport reduces LK expression, and although sqz is dispensable for LK expression in these cells, it can induce ectopic leucokinergic ABLK-like cells when over-expressed. Thus, Sqz appears to be a regulatory factor for neuropeptidergic identity common to all leucokinergic cells, whose function in different cell types is regulated by cell-specific factors.