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Published November 1, 2018 | Supplemental Material + Submitted
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A conserved regulatory program drives emergence of the lateral plate mesoderm

Abstract

Cardiovascular cell lineages emerge with kidney, smooth muscle, and limb skeleton progenitors from the lateral plate mesoderm (LPM). How the LPM emerges during development and how it has evolved to form key lineages of the vertebrate body plan remain unknown. Here, we captured LPM formation by transgenic in toto imaging and lineage tracing using the first pan-LPM enhancer element from the zebrafish gene draculin (drl). drl LPM enhancer-based reporters are specifically active in LPM-corresponding territories of several chordate species, uncovering a universal LPM-specific gene program. Distinct from other mesoderm, we identified EomesA, FoxH1, and MixL1 with BMP/Nodal-controlled Smad activity as minimally required factors to drive drl-marked LPM formation. Altogether, our work provides a developmental and mechanistic framework for LPM emergence and the in vitro differentiation of cardiovascular cell types. Our findings suggest that the LPM may represent an ancient cell fate domain that predates ancestral vertebrates.

Additional Information

The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license. bioRxiv preprint first posted online Feb. 7, 2018. Author Contributions: C.H, K.D.P., S.N., S.B, C.M. designed, performed, and interpreted zebrafish experiments; S.N., E.C., A.B. performed chicken experiments; K. P. performed lightsheet imaging with technical and equipment support by G.S., J.H; E.C.B, K.P., A.F. performed section-based zebrafish lineage tracing; K.W.R, P.M. provided and generated mutants and maternal-zygotic mutant zebrafish; H.J.P, M.B., R.K. designed, performed, and interpreted lamprey experiments; C.R., L.C. designed, performed, and interpreted Ciona experiments; I.K, Z.K designed, performed, and interpreted amphioxus experiments; C.H., K.P., and C.M. assembled and wrote the manuscript with contributions from all co-authors. We thank Sibylle Burger and Seraina Bötschi for technical and husbandry support; the lab of Dr. Stephan Neuhauss for zebrafish husbandry support; the labs of Dr. Esther Stöckli and Dr. Jerome Gros for chicken experimentation support; the ZBM at UZH for imaging support; Dr. Fiona Wardle for input and support on the ChIP-seq panel in Fig. 4E; the lab of Dr. Magdalini Polymenidou for vibratome access; Karolína Ditrychová for cloning the pKD001 construct; Dr. Ashley Bruce, Dr. Rebecca Burdine, and Dr. Michael Tsang for sharing transcription factor constructs; the Stowers Institute histology facility for assistance with lamprey embryo sectioning; and all members of the Mosimann lab for constructive input. This work has been supported by a Swiss National Science Foundation (SNSF) professorship [PP00P3_139093] and SNSF R'Equip grant 150838 (Lightsheet Fluorescence Microscopy), a Marie Curie Career Integration Grant from the European Commission [CIG PCIG14-GA-2013-631984], the Canton of Zürich, the UZH Foundation for Research in Science and the Humanities, the Swiss Heart Foundation, and the ZUNIV FAN/UZH Alumni to C.M; a UZH CanDoc to C.H.; EuFishBioMed and Company of Biologists travel fellowships to K.D.P.; the Stowers Institute (grant #1001) to H.J.P. and R.K.; NIH/NHLBI R01 award HL108643, trans-Atlantic network of excellence award 15CVD01 from the Leducq Foundation to L.C.; a long-term fellowship ALTF 1608-2014 from EMBO to C.R.

Attached Files

Submitted - 261115.full.pdf

Supplemental Material - 261115-1.mp4

Supplemental Material - 261115-2.mp4

Supplemental Material - 261115-3.mp4

Supplemental Material - 261115-4.mp4

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Additional details

Created:
August 19, 2023
Modified:
October 18, 2023