Lee G J, Jun J W, Hyun S
Department of Life Science, Chung-Ang University, Seoul, Korea.
Insect Mol Biol. 2015 Jun;24(3):311-8. doi: 10.1111/imb.12156. Epub 2014 Dec 10.
Metabolic organs such as the liver and adipose tissue produce several peptide hormones that influence metabolic homeostasis. Fat bodies, the Drosophila counterpart of liver and adipose tissues, have been thought to analogously secrete several hormones that affect organismal physiology, but their identity and regulation remain poorly understood. Previous studies have indicated that microRNA miR-8, functions in the fat body to non-autonomously regulate organismal growth, suggesting that fat body-derived humoral factors are regulated by miR-8. Here, we found that several putative peptide hormones known to have mitogenic effects are regulated by miR-8 in the fat body. Most members of the imaginal disc growth factors and two members of the adenosine deaminase-related growth factors are up-regulated in the absence of miR-8. Drosophila insulin-like peptide 6 (Dilp6) and imaginal morphogenesis protein-late 2 (Imp-L2), a binding partner of Dilp, are also up-regulated in the fat body of miR-8 null mutant larvae. The fat body-specific reintroduction of miR-8 into the miR-8 null mutants revealed six peptides that showed fat-body organ-autonomous regulation by miR-8. Amongst them, only Imp-L2 was found to be regulated by U-shaped, the miR-8 target for body growth. However, a rescue experiment by knockdown of Imp-L2 indicated that Imp-L2 alone does not account for miR-8's control over the insect's growth. Our findings suggest that multiple peptide hormones regulated by miR-8 in the fat body may collectively contribute to Drosophila growth.
肝脏和脂肪组织等代谢器官会产生多种影响代谢稳态的肽类激素。脂肪体是果蝇中与肝脏和脂肪组织相对应的器官,一直被认为能类似地分泌几种影响机体生理的激素,但其具体身份和调控机制仍知之甚少。先前的研究表明,微小RNA miR - 8在脂肪体中发挥作用,非自主调节机体生长,这表明脂肪体衍生的体液因子受miR - 8调控。在此,我们发现脂肪体中几种已知具有促有丝分裂作用的假定肽类激素受miR - 8调控。在没有miR - 8的情况下,成虫盘生长因子的大多数成员以及腺苷脱氨酶相关生长因子的两个成员会上调。果蝇胰岛素样肽6(Dilp6)和Dilp的结合伴侣成虫形态发生蛋白 - 晚期2(Imp - L2)在miR - 8基因敲除突变体幼虫的脂肪体中也会上调。将miR - 8特异性重新导入miR - 8基因敲除突变体中,发现有六种肽受miR - 8在脂肪体器官自主调控。其中,仅发现Imp - L2受U形蛋白调控,U形蛋白是miR - 8对身体生长的靶标。然而,通过敲低Imp - L2进行的拯救实验表明,仅Imp - L2并不能解释miR - 8对昆虫生长的控制。我们的研究结果表明,脂肪体中受miR - 8调控的多种肽类激素可能共同影响果蝇的生长。