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SRX24935404: GSM8330952: Dmel pupae P2 1; Drosophila melanogaster; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 11.7M spots, 3.5G bases, 1.5Gb downloads

External Id: GSM8330952_r1
Submitted by: Life sciences, Skolkovo Institute of Science and Technology
Study: Temporal dynamics of gene expression during metamorphosis in two distant Drosophila species
show Abstracthide Abstract
Complete metamorphosis of holometabolous insects is a complex biological process characterized by profound morphological, physiological, and transcriptional changes. To reveal the temporal dynamics of gene expression during this critical developmental transition, a detailed analysis of the developmental transcriptomes of two Drosophila species, Drosophila melanogaster and Drosophila virilis, was conducted. We confirm partial recapitulation of the embryonic transcriptional program in pupae, but instead of the traditional hourglass model, which posits maximal conservation at mid-embryonic stages, at different stages of pupae we observe a more complicated pattern of alternating low and high diversity, resembling an inverted hourglass, or "spindle". This observation challenges the notion of a singular conserved phylotypic period during holometabola ontogeny and underscores the complexity of developmental processes during complete metamorphosis. Notably, recently formed genes (specific to insects) exhibit pronounced expression peaks during mid-pupal development, underscoring their potential role in developmental transitions. Overall design: The dataset includes RNA sequencing samples from wild-type Drosophila melanogaster (Oregon-R) and Drosophila virilis (Strain 9), representing the subgenera Sophophora and Drosophila. Collections included phylotypic embryonic stage, larvae, stages P1 to P5, intermediate, and late pupal stages, as well as five-day-old adult males. All samples were gathered in three biological replicates.
Sample: Dmel pupae P2 1
SAMN41846183 • SRS21639763 • All experiments • All runs
Library:
Name: GSM8330952
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The samples underwent a thorough rinsing process to remove any residual food and yeast, using the PBS buffer. Following this step, total RNA was extracted from the samples using RNAzol RT reagent (MRC, Cincinnati, OH, USA), following the manufacturer's recommended protocols. RNA quality assessments were performed through gel electrophoresis, and the RNA samples were carefully stored in ethanol at -70°C, in preparation for subsequent experimental procedures. Ribosomal RNA depletion was conducted using the NEBNext® Poly(A) mRNA Magnetic Isolation Module. Subsequently, RNA library preparation was carried out with the NEBNext® Ultra™ II Directional RNA Library Prep Kit, and the prepared libraries were sequenced on the Illumina HiSeq4000 platform.
Runs: 1 run, 11.7M spots, 3.5G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR2942233411,719,4733.5G1.5Gb2024-06-17

ID:
33271647

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