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SRX3885542: GSM3081873: st6_rep2; Parasteatoda tepidariorum; RNA-Seq
2 ILLUMINA (Illumina MiSeq) runs: 17.7M spots, 2.2G bases, 870.8Mb downloads

Submitted by: NCBI (GEO)
Study: Developmental profiling of gene expression in embryos of the spider Parasteatoda tepidariorum
show Abstracthide Abstract
The common house spider Parasteatoda tepidariorum is a chelicerate model organism for studying developmental mechanisms and their evolution in arthropods. In contrast to the well-studied model insect, Drosophila melanogaster, embryos of the spider undergo patterning in a cellular environment from early stages (at least after the number of the nuclei increase to 16). Use of spider embryos provide new opportunities to understand the evolution of developmental mechanisms underlying arthropod body plans. This analysis aims to generate genome-scale, developmental profiles of gene expression in embryos of the spider P. tepidariorum, which facilitate a wide range of studies using this spider species. Overall design: The genome of P. tepidariorum has been sequenced, with gene models annotated (Schwager et al., 2017, BMC Biol. 15, 62). Embryonic development of P. tepidariorum has been divided into more than 10 stages (Akiyama-Oda and Oda, 2003, Development 130, 1735-1747; Mittmann and Wolff, 2012, Dev. Genes Evol. 222, 189-216). Two developmental series of mRNA (stage (st) 1, st2, st3, st4, st5 early, st5 late, st6, st7, st8, st10) were independently obtained from two pairs of parents and analyzed by RNA sequencing (RNA-Seq). Obtained reads were mapped to the genome assembly of P. tepidariorum (Ptep_1.0) and counted against AUGUSTUS gene models (Schwager et al., 2017, BMC Biol. 15, 62).
Sample: st6_rep2
SAMN08865680 • SRS3124686 • All experiments • All runs
Library:
Instrument: Illumina MiSeq
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Poly(A) mRNA was extracted using the Dynabeads mRNA DIRECT Kit (Ambion) from 10-100 embryos of each successive developmental stage. mRNA was fragmented using the NEBNext Rnase III RNA Fragmentation Module (New England BioLabs). Sequencing libraries were constructed from fragmented RNA using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England BioLabs) and NEBNext Multiplex Oligos for Illumina (Index Primers Set 1, New England BioLabs).
Experiment attributes:
GEO Accession: GSM3081873
Links:
Runs: 2 runs, 17.7M spots, 2.2G bases, 870.8Mb
Run# of Spots# of BasesSizePublished
SRR69413518,423,5971G393.8Mb2018-04-06
SRR69413529,283,3091.1G477Mb2018-04-06

ID:
5338401

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