bioRxiv Science⌕ Search

Biology subjects

Pruenster, M. M.

Publications and source records attributed to Pruenster, M. M..

2 recordsLinked to original sources

Chordin-mediated BMP shuttling patterns the secondary body axis in a cnidarian

BMP signaling patterns secondary body axes throughout Bilateria and, strikingly, in the bilaterally symmetric corals and sea anemones - members of the bilaterian sister clade Cnidaria. It has been suggested that the secondary, "directive" axis in the sea anemone Nematostella vectensis requires Chordin-mediated "shuttling" of BMP ligands, like in Drosophila or frog, however, an alternative "local inhibition" model is also possible. To choose between these two options, we generated localized Chordin sources in the Chordin morphant background and showed that in the presence of BMP ligands in Nematostella, mobile Chordin is necessary and sufficient to establish a peak of BMP signaling at the side of the embryo opposing the Chordin source. In contrast, membrane-tethered Chordin-CD2 promotes weak BMP signaling within the Chordin-CD2 source. These results provide the first mechanistic evidence for BMP shuttling in a cnidarian and suggest that BMP shuttling may have been functional in the cnidarian-bilaterian ancestor.

developmental biology↗

Modular co-option of cardiopharyngeal genes during non-embryonic myogenesis

BackgroundIn chordates cardiac and body muscles arise from different embryonic origins. Myogenesis can in addition be triggered in adult organisms, during asexual development or regeneration. In the non-vertebrate ascidians, muscles originate from embryonic precursors regulated by a conserved set of genes that orchestrate cell behavior and dynamics during development. In colonial ascidians, besides embryogenesis and metamorphosis, an adult can propagate asexually via blastogenesis, skipping embryo and larval stages, and form anew the adult body, including the complete body musculature.\n\nResultsTo investigate the cellular origin and mechanisms that trigger non-embryonic myogenesis, we followed the expression of ascidian myogenic genes during Botryllus schlosseri blastogenesis, and reconstructed the dynamics of muscle precursors. Based on the expression dynamics of Tbx1/10, Ebf, Mrf, Myh3 for body wall and of FoxF, Tbx1/10, Nk4, Myh2 for heart development we show that the embryonic factors regulating myogenesis are only partially co-opted in blastogenesis, and propose that the cellular precursors contributing to heart or body muscles have different origins.\n\nConclusionsRegardless of the developmental pathway, non-embryonic myogenesis shares a similar molecular and anatomical setup as embryonic myogenesis, but implements co-option and loss of molecular modules.

developmental biology↗