RT Journal Article SR Electronic T1 An ancestral apical brain region contributes to the central complex under the control of foxQ2 in the beetle Tribolium castaneum JF bioRxiv FD Cold Spring Harbor Laboratory SP 661199 DO 10.1101/661199 A1 Bicheng He A1 Marita Buescher A1 Max Stephen Farnworth A1 Frederic Strobl A1 Ernst Stelzer A1 Nikolaus Dieter Bernhard Koniszewski A1 Dominik Mühlen A1 Gregor Bucher YR 2019 UL http://biorxiv.org/content/early/2019/06/06/661199.abstract AB The genetic control of anterior brain development is highly conserved throughout animals. For instance, a conserved anterior gene regulatory network specifies the ancestral neuroendocrine center of animals and the apical organ of marine organisms. However, its contribution to the brain in non-marine animals has remained elusive. Here, we study the function of the Tc-foxQ2 forkhead transcription factor, a key regulator of the anterior gene regulatory network of insects. We characterized four distinct types of Tc-foxQ2 positive neural progenitor cells based on differential co-expression with Tc-six3/optix, Tc-six4, Tc-chx/vsx, Tc-nkx2.1/scro, Tc-ey, Tc-rx and Tc-fez1. An enhancer trap line built by genome editing marked Tc-foxQ2 positive neurons, which projected through the primary brain commissure and later through a subset of commissural fascicles. Eventually, they contributed to the central complex. Strikingly, in Tc-foxQ2 RNAi knock-down embryos the primary brain commissure did not split and subsequent development of midline brain structures stalled. Our work establishes foxQ2 as a key regulator of brain midline structures, which distinguish the protocerebrum from segmental ganglia. Unexpectedly, our data suggest that the central complex evolved by integrating neural cells from an ancestral anterior neuroendocrine center.Summary statement An ancestral neuroendocrine center contributes to the evolution of the central complex. foxQ2 is a gene required for the development of midline structures of the insect brain, which distinguish protocerebrum from segmental ganglia.