TY - JOUR
T1 - Gene regulatory control in the sea urchin aboral ectoderm
T2 - Spatial initiation, signaling inputs, and cell fate lockdown
AU - Ben-Tabou de-Leon, Smadar
AU - Su, Yi Hsien
AU - Lin, Kuan Ting
AU - Li, Enhu
AU - Davidson, Eric H.
N1 - Funding Information: Research was supported by NIH grant HD-037105 to EHD and by National Science Council grants 99-2627-B-001-003 and 1 01-2923-B-001-004-MY2 to YS.
PY - 2013/2/1
Y1 - 2013/2/1
N2 - The regulation of oral-aboral ectoderm specification in the sea urchin embryo has been extensively studied in recent years. The oral-aboral polarity is initially imposed downstream of a redox gradient induced by asymmetric maternal distribution of mitochondria. Two TGF-Β signaling pathways, Nodal and BMP, are then respectively utilized in the generation of oral and aboral regulatory states. However, a causal understanding of the regulation of aboral ectoderm specification has been lacking. In this work control of aboral ectoderm regulatory state specification was revealed by combining detailed regulatory gene expression studies, perturbation and cis-regulatory analyses. Our analysis illuminates a dynamic system where different factors dominate at different developmental times. We found that the initial activation of aboral genes depends directly on the redox sensitive transcription factor, hypoxia inducible factor 1α (HIF-1α). Two BMP ligands, BMP2/4 and BMP5/8, then significantly enhance aboral regulatory gene transcription. Ultimately, encoded feedback wiring lockdown the aboral ectoderm regulatory state. Our study elucidates the different regulatory mechanisms that sequentially dominate the spatial localization of aboral regulatory states.
AB - The regulation of oral-aboral ectoderm specification in the sea urchin embryo has been extensively studied in recent years. The oral-aboral polarity is initially imposed downstream of a redox gradient induced by asymmetric maternal distribution of mitochondria. Two TGF-Β signaling pathways, Nodal and BMP, are then respectively utilized in the generation of oral and aboral regulatory states. However, a causal understanding of the regulation of aboral ectoderm specification has been lacking. In this work control of aboral ectoderm regulatory state specification was revealed by combining detailed regulatory gene expression studies, perturbation and cis-regulatory analyses. Our analysis illuminates a dynamic system where different factors dominate at different developmental times. We found that the initial activation of aboral genes depends directly on the redox sensitive transcription factor, hypoxia inducible factor 1α (HIF-1α). Two BMP ligands, BMP2/4 and BMP5/8, then significantly enhance aboral regulatory gene transcription. Ultimately, encoded feedback wiring lockdown the aboral ectoderm regulatory state. Our study elucidates the different regulatory mechanisms that sequentially dominate the spatial localization of aboral regulatory states.
KW - Cis-regulatory analysis
KW - Developmental control
KW - Ectoderm specification
KW - Gene regulatory networks
KW - Sea urchin
UR - http://www.scopus.com/inward/record.url?scp=84872417517&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.ydbio.2012.11.013
DO - https://doi.org/10.1016/j.ydbio.2012.11.013
M3 - Article
C2 - 23211652
SN - 0012-1606
VL - 374
SP - 245
EP - 254
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -