rdgB knockdown in neurons reduced nocturnal sleep in Drosophila melanogaster
rdgB knockdown in neurons reduced nocturnal sleep in Drosophila melanogaster
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DOI:
10.1016/j.bbrc.2022.12.043
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发表时间:
2022-12-29
影响因子:
3.1
通讯作者:
Kume, Kazuhiko
中科院分区:
文献类型:
--
作者:
Kobayashi, Riho;Yamashita, Yuko;Kume, Kazuhiko
Recent studies revealed behaviorally defined sleep is conserved across broad species from insect to human. For evolutional analysis, it is critical to determine how homologous genes regulate the homol-ogous function among species. Drosophila melanogaster shares numerous sleep related genes with mammals including Sik3, salt-inducible kinase 3, whose mutation caused long sleep both in mouse and fruit fly. The Drosophila rdgB (retinal degeneration B) encodes a membrane-associated phosphatidyli-nositol transfer protein and its mutation caused light-induced degeneration of photoreceptor cells. rdgB mutation also impaired phototransduction and olfactory behavior, indicating rdgB is involved in the normal neural transmission. Mammalian rdgB homologue, Pitpnm2 (phosphatidylinositol transfer pro-tein membrane-associated 2) was discovered as one of SNIPPs (sleep-need index phosphoproteins), suggesting its role in sleep. Here, we show that rdgB is involved in sleep regulation in Drosophila. Pan -neuronal and mushroom body (MB) specific rdgB knockdown decreased nocturnal sleep. MB neurons play a dominant role, since the rescue of rdgB expression only in MB neurons in pan-neuronal knock-down reversed the sleep reducing effect of rdgB knockdown. These results revealed the sleep-related function of rdgB in Drosophila which may be conserved across species.(c) 2022 Elsevier Inc. All rights reserved.