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Sample GSM5733324 Query DataSets for GSM5733324
Status Public on Jul 13, 2022
Title dme.WT.pSC.rep4
Sample type SRA
 
Source name Late primary spermatocyte cyst
Organism Drosophila melanogaster
Characteristics genotype: dme.WT
age: 2-3 days after eclosion
Growth protocol All the flies were raised using cornmeal-sucrose-yeast medium at 25°C with a 12-h light-dark cycle throughout this study.
Extracted molecule total RNA
Extraction protocol 1) For testis samples, adult flies 3-5 days after eclosion were allowed to mate and then testes were dissected in drops of 1× phosphate-buffered saline (PBS) with two pairs of Dumont #5 forceps. For the extraction of total RNA, 20-25 pairs of testes were pooled as a sample. RNeasy Micro Kit (QIAGEN, German) was used for RNA extraction following the manufacturer’s instructions. 2) For single-cyst samples, testes from mated male flies 2-3 days after eclosion were dissected. Two tungsten micro-needles (World Precision Instruments, USA) were used to tear the muscle sheath layer, resulting in germ cell cysts spilling into a drop of 1× phosphate-buffered saline (PBS). The cysts were viewed using an inverted microscope (Leica DMI4000 microscope), and were picked using a glass capillary (BJ-40, Beijing Zhengtian Yi Science and Trade Co. LTD) pulled by a Sutter instrument P-30 with the following parameters: heat#1 = 930; pull = 909. The cysts were staged using the criteria as follows: spermatogonia (SG), 16-cell cysts with cells of <10 μm in diameter for D. melanogaster and < 8 μm in diameter for D. simulans; late primary spermatocytes (pSC), 16-cell cysts with cells of 22-25 μm in diameter; round spermatids (rST), cysts with much more than 32 round or nearly round cells of 14-16 μm in diameter; and elongating spermatids (eST), bundles of 250-350 μm in length. The staged single cyst was transferred into PCR tube by pushing the syringe which was connected with the glass capillary by an infusion tube. Cell lysis, reverse transcription, PCR preamplification and purification of PCR products were conducted using Discover-sc™ WTA Kit V2 (Vazyme Biotech, China) according to the user’s guides.
1) For testis samples, RNA libraries were prepared for sequencing using standard Illumina protocols. 2) For single-cyst samples, RNA-seq libraries were constructed using TruePrep™ DNA Library Prep Kit V2 for Illumina® (Vazyme Biotech, China) and an input of 1 ng amplified cDNAs.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model HiSeq X Ten
 
Data processing After removing adapters by Trimmomatic (version 0.36, used parameters 2:30:10:1:true MINLEN:75), short reads were mapped to the corresponding reference genomes of D. melanogaster (r6.36) and D. simulans (r2.02), respectively, using HISAT (version 2.2.0, --dta and other default parameters).
Expression abundance of each gene was calculated as FPKM and TPM with StringTie (version 2.1.4, used -e and other default parameters). The annotation files of dmel-all-r6.36.gtf and dsim-all-r2.02.gtf were downloaded from FlyBase (http://flybase.org/) in October 2020.
HTSeq (version 0.6.0, used parameters -f bam -r name -s no -t exon -m union) was applied to count mapped reads for each gene.
Genome_build: D. melanogaster (r6.36) and D. simulans (r2.02)
Supplementary_files_format_and_content: Tab-delimited text files include FPKM and TPM values for each gene
Supplementary_files_format_and_content: Matrix table with raw gene counts for every gene and every sample
 
Submission date Dec 14, 2021
Last update date Jul 13, 2022
Contact name Yumei Huang
E-mail(s) hyumei2@mail2.sysu.edu.cn
Organization name Sun Yat-sen University
Street address Haizhu District Xingangxi Road No. 135
City Guangzhou
State/province Guangdong
ZIP/Postal code 510275
Country China
 
Platform ID GPL23702
Series (1)
GSE190885 Trans regulatory evolution of a young microRNA during Drosophila spermatogenesis 
Relations
BioSample SAMN24024660
SRA SRX13437745

Supplementary file Size Download File type/resource
GSM5733324_dme.WT.pSC.4.txt.gz 429.9 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record
Processed data provided as supplementary file

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