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SRX14166064: GSM5897778: 8 hpf [Pm8h]; Patiria miniata; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 423.2M spots, 127G bases, 57.3Gb downloads

External Id: GSM5897778_r1
Submitted by: Molecular Biology, Cell Biology & Biochemistry, Brown University
Study: Distinct mechanisms of germ cell factor regulation for an inductive germ cell fate
show Abstracthide Abstract
Here we employed single cell RNA sequencing to identify the transcriptional program of Nanos and Vasa positive cells and their changes during development. Our single cell sequencing analysis of six developmental stages in P. miniata revealed cell types derived from the three germ layers and expression of the germ cell genes Nanos and Vasa. We used these datasets to parse out 20 cell lineages of the embryo identified by this approach and to focus on the key transitions of germ cell gene expression and test their coexpression with key signaling components. Overall design: Adult Patiria miniata animals were collected by either Peter Halmay ([email protected]) or Josh Ross ([email protected]) off the Californian coast. Embryos were cultured essentially as described previously (Fresques et al., 2016). Embryos were cultured in filtered (0.2micron) sea water collected at the Marine Biological laboratories in Woods Hole MA, until the appropriate stage for dissociation. All embryos used in the study resulted from mating of one male and one female. Multiple fertilizations were initiated in this study and timed such that the appropriate stages of embryonic development were reached at a common endpoint. The embryos were then collected and washed twice with calcium-free sea water, and then suspended hyalin-extraction media (HEM) for 10-15 minutes, depending on the stage of dissociation. When cells were beginning to dissociate, the embryos were collected and washed in 0.5M NaCl, gently sheared with a pipette, run through a 40micron Nitex mesh, counted on a hemocytometer, and diluted to reach the appropriate concentration for the scRNA-seq protocol. Equal numbers of embryos were used in each time point and at no time were cells or embryos pelleted in a centrifuge (Oulhen et al., 2019).
Sample: 8 hpf [Pm8h]
SAMN25894941 • SRS11990192 • All experiments • All runs
Organism: Patiria miniata
Library:
Name: GSM5897778
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Single cell encapsulation was performed using the Chromium Single Cell Chip B kit on the 10x Genomics Chromium Controller. Single cell cDNA and libraries were prepared using the Chromium Single Cell 3' Reagent kit v3 Chemistry. Libraries were sequenced by Genewiz on the Illumina Hiseq (2x150 bp paired-end runs).
Runs: 1 run, 423.2M spots, 127G bases, 57.3Gb
Run# of Spots# of BasesSizePublished
SRR18011746423,203,522127G57.3Gb2022-11-16

ID:
19972034

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