| Abstract: | 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. |
