TY - JOUR
T1 - Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints
AU - Genikhovich, Grigory
AU - Fried, Patrick
AU - Prünster, Maria Mandela
AU - Schinko, Johannes
AU - Gilles, Anna
AU - Fredman, David
AU - Meier, Karin
AU - Iber, Dagmar
AU - Technau, Ulrich
N1 - Publisher Copyright:
© 2015 The Authors.
PY - 2015/3/17
Y1 - 2015/3/17
N2 - BMP signaling plays a crucial role in the establishment of the dorso-ventral body axis in bilaterally symmetricanimals. However, the topologies of the bone morphogenetic protein (BMP) signaling networks vary drastically in different animal groups, raising questions about the evolutionary constraints and evolvability of BMP signaling systems. Using loss-of-function analysis and mathematical modeling, we show that two signaling centers expressing different BMPs and BMP antagonists maintain the secondary axis of the sea anemone Nematostella. We demonstrate that BMP signaling is required for asymmetric Hox gene expression and mesentery formation. Computational analysis reveals that network parameters related to BMP4 and Chordin are constrained both in Nematostella and Xenopus, while those describing the BMP signaling modulators can vary significantly. Notably, only chordin, but not bmp4 expression needs to be spatially restricted for robust signaling gradient formation. Our data provide an explanation of the evolvability of BMP signaling systems in axis formation throughout Eumetazoa.
AB - BMP signaling plays a crucial role in the establishment of the dorso-ventral body axis in bilaterally symmetricanimals. However, the topologies of the bone morphogenetic protein (BMP) signaling networks vary drastically in different animal groups, raising questions about the evolutionary constraints and evolvability of BMP signaling systems. Using loss-of-function analysis and mathematical modeling, we show that two signaling centers expressing different BMPs and BMP antagonists maintain the secondary axis of the sea anemone Nematostella. We demonstrate that BMP signaling is required for asymmetric Hox gene expression and mesentery formation. Computational analysis reveals that network parameters related to BMP4 and Chordin are constrained both in Nematostella and Xenopus, while those describing the BMP signaling modulators can vary significantly. Notably, only chordin, but not bmp4 expression needs to be spatially restricted for robust signaling gradient formation. Our data provide an explanation of the evolvability of BMP signaling systems in axis formation throughout Eumetazoa.
UR - http://www.scopus.com/inward/record.url?scp=84925133695&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2015.02.035
DO - 10.1016/j.celrep.2015.02.035
M3 - Article
VL - 10
SP - 1646
EP - 1654
JO - Cell Reports
JF - Cell Reports
SN - 2211-1247
IS - 10
ER -