Pan-neuronal knockdown of Ras GTPase-activating protein 1 alters Drosophila activity and sleep behavior

被引:0
|
作者
Lagunas-Rangel, Francisco Alejandro [1 ,2 ]
机构
[1] Ctr Invest & Estudios Avanzados Inst Politecn Nacl, Dept Genet & Mol Biol, Mexico City, Mexico
[2] Ctr Invest & Estudios Avanzados Inst Politecn Nacl, Dept Genet & Mol Biol, Ave Inst Politecn Nacl 2508, Mexico City 07360, Mexico
关键词
circulating glucose; dopamine; feeding behavior; fly movement; RasGAP1; LOCOMOTOR-ACTIVITY; SIGNALING PATHWAY; LIFE-SPAN; RECEPTOR; GROWTH; BRAIN; OBESITY;
D O I
10.1002/arch.22001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ras signaling pathways are involved in numerous cellular functions and, for this reason, are highly regulated. In addition to alterations in the Ras proteins themselves, defects in Ras regulatory proteins, such as GTPase-activating proteins (GAPs) and guanine nucleotide exchange factors (GEFs), may be relevant to disease development. Drosophila RasGAP1 is a protein with important physiological implications in flies due to its participation in the signaling of different pathways. In this work, the changes that occur in Drosophila behavior by reducing the pan-neuronal expression of RasGAP1 were investigated. Thus, RasGAP1 knockdown was found to cause a significant increase in total activity (p <= 0.001) and activity at 30 min (p <= 0.001). In contrast, total sleep duration (p <= 0.001), sleep within 30 min (p <= 0.001), and mean duration of sleep episodes (p <= 0.0001) were all reduced. Furthermore, circulating levels of glucose (p <= 0.05) and triacylglycerol (p <= 0.05) were found to be elevated. No significant changes were found in feeding behavior, food source selection, trehalose, or glycogen levels. All these results show new functions of RasGAP1 in Drosophila physiology and may also serve to explain some functions of human orthologs (RasGAP2/3 [RASA2/3]).
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