Abstract
Gene expression is regulated at various levels, including post-transcriptional mRNA modifications, where m(6)A methylation is the most common modification of mRNA. The m(6)A methylation regulates multiple stages of mRNA processing, including splicing, export, decay, and translation. How m(6)A modification is involved in insect development is not well known. We used the red flour beetle, Tribolium castaneum, as a model insect to identify the role of m(6)A modification in insect development. RNA interference (RNAi)-mediated knockdown of genes coding for m(6)A writers (m(6)A methyltransferase complex, depositing m(6)A to mRNA) and readers (YTH-domain proteins, recognizing and executing the function of m(6)A) was conducted. Knockdown of most writers during the larval stage caused a failure of ecdysis during eclosion. The loss of m(6)A machinery sterilized both females and males by interfering with the functioning of reproductive systems. Females treated with dsMettl3, the main m(6)A methyltransferase, laid significantly fewer and reduced-size eggs than the control insects. In addition, the embryonic development in eggs laid by dsMettl3 injected females was terminated in the early stages. Knockdown studies also showed that the cytosol m(6)A reader, YTHDF, is likely responsible for executing the function of m(6)A modifications during insect development. These data suggest that m(6)A modifications are critical for T. castaneum development and reproduction.