Laboratory of Physiological Chemistry, de Duve Institute, Université Catholique de Louvain, Bruxelles, Belgium.
Department of Biology and Program in Biochemistry, Vassar College, Poughkeepsie, New York, USA.
Dev Dyn. 2021 Nov;250(11):1634-1650. doi: 10.1002/dvdy.344. Epub 2021 Apr 16.
miR-33 family members are well characterized regulators of cellular lipid levels in mammals. Previous studies have shown that overexpression of miR-33 in Drosophila melanogaster leads to elevated triacylglycerol (TAG) levels in certain contexts. Although loss of miR-33 in flies causes subtle defects in larval and adult ovaries, the effects of miR-33 deficiency on lipid metabolism and other phenotypes impacted by metabolic state have not yet been characterized.
We found that loss of miR-33 predisposes flies to elevated TAG levels, and we identified genes involved in TAG synthesis as direct targets of miR-33, including atpcl, midway, and Akt1. miR-33 mutants survived longer upon starvation but showed greater sensitivity to an oxidative stressor. We also found evidence that miR-33 is a negative regulator of cuticle pigmentation and that miR-33 mutants show a reduction in interfollicular stalk cells during oogenesis.
Our data suggest that miR-33 is a conserved regulator of lipid homeostasis, and its targets are involved in both degradation and synthesis of fatty acids and TAG. The constellation of phenotypes involving tissues that are highly sensitive to metabolic state suggests that miR-33 serves to prevent extreme fluctuations in metabolically sensitive tissues.
miR-33 家族成员是哺乳动物细胞脂质水平的重要调节因子。先前的研究表明,在果蝇中过表达 miR-33 会导致某些情况下三酰基甘油 (TAG) 水平升高。尽管果蝇中 miR-33 的缺失会导致幼虫和成虫卵巢的细微缺陷,但 miR-33 缺乏对脂质代谢和其他受代谢状态影响的表型的影响尚未得到表征。
我们发现 miR-33 的缺失使果蝇更容易出现 TAG 水平升高的情况,并且我们鉴定了参与 TAG 合成的基因是 miR-33 的直接靶标,包括 atpcl、midway 和 Akt1。饥饿时,miR-33 突变体的存活率更高,但对氧化应激剂的敏感性更高。我们还发现证据表明 miR-33 是表皮色素沉着的负调节剂,并且 miR-33 突变体在卵发生过程中表现出滤泡间柄细胞减少。
我们的数据表明,miR-33 是脂质稳态的保守调节剂,其靶基因参与脂肪酸和 TAG 的降解和合成。涉及对代谢状态高度敏感的组织的表型组合表明,miR-33 有助于防止代谢敏感组织中代谢的剧烈波动。