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Developmental single-cell transcriptomics in the Lytechinus variegatus sea urchin embryo.

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Date
2021-08-31
Authors
Massri, Abdull J
Greenstreet, Laura
Afanassiev, Anton
Berrio, Alejandro
Wray, Gregory A
Schiebinger, Geoffrey
McClay, David R
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Abstract
Using scRNA-seq coupled with computational approaches, we studied transcriptional changes in cell states of sea urchin embryos during development to the larval stage. Eighteen closely spaced time points were taken during the first 24 hours of development of Lytechinus variegatus (Lv). Developmental trajectories were constructed using Waddington-OT, a computational approach to "stitch" together developmental timepoints. Skeletogenic and primordial germ cell trajectories diverged early in cleavage. Ectodermal progenitors were distinct from other lineages by sixth cleavage, though a small percentage of ectoderm cells briefly co-expressed endoderm markers indicating an early ecto-endoderm cell state, likely in cells originating from the equatorial region of the egg. Endomesoderm cells originated at 6th cleavage also and this state persisted for more than two cleavages, then diverged into distinct endoderm and mesoderm fates asynchronously, with some cells retaining an intermediate specification status until gastrulation. 79 of 80 genes (99%) examined, and included in published developmental gene regulatory networks (dGRNs), are present in the Lv-scRNA-seq dataset, and expressed in the correct lineages in which the dGRN circuits operate.
Type
Journal article
Subject
Cell lineage
Gene regulatory networks
ScRNA-seq
Sea urchin embryo
Permalink
https://hdl.handle.net/10161/23878
Published Version (Please cite this version)
10.1242/dev.198614
Publication Info
Massri, Abdull J; Greenstreet, Laura; Afanassiev, Anton; Berrio, Alejandro; Wray, Gregory A; Schiebinger, Geoffrey; & McClay, David R (2021). Developmental single-cell transcriptomics in the Lytechinus variegatus sea urchin embryo. Development (Cambridge, England). 10.1242/dev.198614. Retrieved from https://hdl.handle.net/10161/23878.
This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.
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Scholars@Duke

McClay

David R. McClay Jr.

Arthur S. Pearse Distinguished Professor of Biology
We ask how the embryo works. Prior to morphogenesis the embryo specifies each cell through transcriptional regulation and signaling. Our research builds gene regulatory networks to understand how that early specification works. We then ask how this specification programs cells for their morphogenetic movements at gastrulation, and how the cells deploy patterning information. Current projects examine 1) novel signal transduction mechanisms that establish and maintain embryonic bound
Wray

Gregory Allan Wray

Professor of Biology
I study the evolution of genes and genomes with the broad aim of understanding the origins of biological diversity. My approach focuses on changes in the expression of genes using both empirical and computational approaches and spans scales of biological organization from single nucleotides through gene networks to entire genomes. At the finer end of this spectrum of scale, I am focusing on understanding the functional consequences and fitness components of specific genetic variants within reg
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