PT - JOURNAL ARTICLE AU - Maria Ninova AU - Matthew Ronshaugen AU - Sam Griffiths-Jones TI - <em>Tribolium castaneum</em> as a model for microRNA evolution, expression and function during short germband development AID - 10.1101/018424 DP - 2015 Jan 01 TA - bioRxiv PG - 018424 4099 - http://biorxiv.org/content/early/2015/04/22/018424.short 4100 - http://biorxiv.org/content/early/2015/04/22/018424.full AB - MicroRNAs are well-established players in the development of multicellular animals. Most of our understanding of microRNA function in arthropod development comes from studies in Drosophila. Despite their advantages as model systems, the long germband embryogenesis of fruit flies is an evolutionary derived state restricted to several holometabolous insect lineages. MicroRNA evolution and expression across development in animals exhibiting the ancestral and more widespread short germband mode of embryogenesis has not been characterized. We sequenced small RNA libraries of oocytes and successive time intervals covering the embryonic development of the short germband model organism, the red flour beetle Tribolium castaneum. We analysed the evolution and temporal expression of the microRNA complement, and sequenced libraries of total RNA to investigate the relationships with microRNA target expression. We show microRNA maternal loading and sequence-specific 3’-end non-template oligoadenylation of maternally deposited microRNAs that is conserved between Tribolium and Drosophila. We further uncover large clusters encoding multiple paralogs from several Tribolium-specific microRNA families expressed during a narrow interval of time immediately after the activation of zygotic transcription. These novel microRNAs, together with several early expressed conserved microRNAs, target a significant number of maternally deposited transcripts. Comparison with Drosophila shows that microRNA-mediated maternal transcript targeting is a conserved phenomenon in insects, but the number and sequences of microRNAs involved in this process have diverged. The expression of fast-evolving and species-specific microRNAs in the early blastoderm of T. castaneum is consistent with previous findings in Drosophila and shows that the unique permissiveness for microRNA innovation at this stage is a conserved phenomenon.