Evolution of the back-to-belly axis

Evolution of the back-to-belly axis
By analysis of sea anemones, the origin of the second axis of the body of humans and animals were revealed. Credit: Copyright: Grigory Genikhovich

Most animals have a dorso-ventral (back-to-belly) body axis, which determines for instance the localized position of the central nervous system, dorsal in humans, ventral in insects. Surprisingly, despite enormous morphological differences, the same signaling molecules of Bone morphogenetic protein (BMP) molecules establishes the dorso-ventral axis including the central nervous system in both insects and vertebrates, which led to the conclusion that this molecular mechanism was already present in the common ancestor.

How deep can we trace the origin of the dorso-ventral axis? It turned out that provides the answer: "By analysing the role of BMPs during embryogenesis of the sea anemone Nematostella vectensis, we could get insights into the evolution of animal body axes." says Ulrich Technau of the Department of Molecular Evolution and Development at the University of Vienna.

Two body axes in the sea anemone

Sea anemones belong to the phylum of cnidarians, such as corals, hydra and jellyfish and they evolved at least 600 Million years ago. Most textbooks consider cnidarians as radially symmetric, i.e. they have one apparent body axis, the oral-aboral axis. In their newest study in Cell Reports the scientists found that the sea anemone has even several BMPs and BMP antagonists. During early embryogenesis, these signaling molecules establish a complex interaction network to build up an activity gradient - "yet, perpendicular to the main body axis" explains Ulrich Technau. On the basis of detailed genetic analyses the authors conclude that the BMP is used for the establishment of a second body axis. However, the gradient of is interpreted and used differently in the sea anemone compared to vertebrates and insects.

Evolution of the back-to-belly axis
Top image: The transcripts of a BMP gene NvDpp and of a Hox gene NvHoxE are localized to opposite end of the directive axis in the Nematostella larva. Middle: The signaling activity of BMP (red staining) and NvHoxE protein (green staining) are located on the same side of the directive axis. Bottom: Suppression of NvDpp translation results in the loss of BMP signaling and NvHoxE protein. Asterisks denote the mouth of the larva. Two bottom images are taken at the Core Imaging Facility of the Faculty of Life Sciences. Credit: Copyright: Grigory Genikhovich

Mesenteries instead of central nervous system

Instead of determining the position of the , the sea anemone uses the BMP activity gradient to determine the position and formation of so called "mesenteries", which are epithelial folds that reach into the gastric cavity, harboring retractor muscles and gonads.

Surprisingly, the BMP-gradient regulates the regional activation of "Hox genes", which are famous for their role in specifying the segmental identity along the main body axis, such as wings and legs in flies or ribs and limbs in vertebrates. This connection of a signaling system of the dorso-ventral body axis with regulator genes of the anterior-posterior body axis is surprising and unexpected. The researchers then asked how such signaling networks could have evolved over hundreds of millions of years in order to give rise to quite different morphological structures in various animal lineages. In a collaboration with mathematicians of the ETH Zürich they could show in mathematical modelling, which parts of the network were kept constant until today and which could be changed, in order to evolve new functions. "The BMP network is not only an example of a signaling system that is involved in axis formation for more than 600 Million years, but we can also learn from the comparison with sea anemones, how such important networks could evolve" summarizes Technau.


Explore further

Surprise gene finding on "back or belly" decision in sea anemones

More information: Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints. Grigory Genikhovich, Patrick Fried, M. Mandela Prünster, Johannes B. Schinko, Anna F. Gilles, David Fredman, Karin Meier, Dagmar Iber und Ulrich Technau. In: Cell Reports 10. 1-9, 17. März 2015.
DOI: dx.doi.org/10.1016/j.celrep.2015.02.035
Journal information: Cell Reports

Citation: Evolution of the back-to-belly axis (2015, March 18) retrieved 15 December 2019 from https://phys.org/news/2015-03-evolution-back-to-belly-axis.html
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