Rhythmic Behavior Is Controlled by the SRm160 Splicing Factor in Drosophila melanogaster

Author:

Beckwith Esteban J11,Hernando Carlos E1,Polcowñuk Sofía2,Bertolin Agustina P3,Mancini Estefania1,Ceriani M Fernanda2,Yanovsky Marcelo J1

Affiliation:

1. Laboratorio de Genómica Comparativa del Desarrollo Vegetal, Fundación Instituto Leloir, Instituto de Investigeciones Bioquimicas de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires 1417, Argentina

2. Laboratorio de Genética del Comportamiento, Fundación Instituto Leloir, Instituto de Investigeciones Bioquimicas de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires 1417, Argentina

3. Laboratorio de Ciclo Celular y Estabilidad Genómica, Fundación Instituto Leloir, Instituto de Investigaciones Bioquímica de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires 1417, Argentina

Abstract

Abstract Animals have evolved neural circuits that allow them to generate adaptive behaviors to their natural environment. Specific neuronal clusters depend on..... Circadian clocks organize the metabolism, physiology, and behavior of organisms throughout the day–night cycle by controlling daily rhythms in gene expression at the transcriptional and post-transcriptional levels. While many transcription factors underlying circadian oscillations are known, the splicing factors that modulate these rhythms remain largely unexplored. A genome-wide assessment of the alterations of gene expression in a null mutant of the alternative splicing regulator SR-related matrix protein of 160 kDa (SRm160) revealed the extent to which alternative splicing impacts on behavior-related genes. We show that SRm160 affects gene expression in pacemaker neurons of the Drosophila brain to ensure proper oscillations of the molecular clock. A reduced level of SRm160 in adult pacemaker neurons impairs circadian rhythms in locomotor behavior, and this phenotype is caused, at least in part, by a marked reduction in period (per) levels. Moreover, rhythmic accumulation of the neuropeptide PIGMENT DISPERSING FACTOR in the dorsal projections of these neurons is abolished after SRm160 depletion. The lack of rhythmicity in SRm160-downregulated flies is reversed by a fully spliced per construct, but not by an extra copy of the endogenous locus, showing that SRm160 positively regulates per levels in a splicing-dependent manner. Our findings highlight the significant effect of alternative splicing on the nervous system and particularly on brain function in an in vivo model.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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