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SRX10724171: GSM5273495: GE2_oviducts of Yun7Ge; Bombyx mori; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 34.5M spots, 10.3G bases, 4.2Gb downloads

Submitted by: NCBI (GEO)
Study: Differentially expressed genes (DEGs) in oviducts of Yun7 and its giant egg mutant Yun7Ge of silkworm, Bombyx mori
show Abstracthide Abstract
Yun7Ge (Yun7Ge is represented by Ge in the high-throughput sequencing results) is a giant egg mutant found in the silkworm variety Yun7 (Yun7 is represented by Se in the high-throughput sequencing results). The amount of laid eggs and the hatching rate of Yun7Ge are reduced, which is not conducive to the reproduction. The target gene controlling giant egg trait is located on the Z chromosome (chromosome 1) was determined through genetic analysis. To find mutant gene and explore the relationship between mutant gene and giant egg trait, the differentially expressed genes (DEGs) in the oviducts of Yun7 and Yun7Ge were analyzed by high-throughput sequencing, and two replicates were set for each sample. |log 2|>1, the value of FPKM>100 and the genes were up-regulated or down-regulated in giant eggs of the two replicates as the standard for screening DEGs. A total of 65 DEGs were screened. Among these DEGs, 7 genes were up-regulated and 58 genes were down-regulated in giant eggs. These DEGs were classified according to the chromosome where the genes are located. The results showed that there was only one DEG (PHYHD1) on chromosome Z, and it was almost not expressed in giant eggs. Interestingly, there were 35 DEGs on chromosome 2, including 25 chorion genes, and these 25 genes are all down-regulated. After knocking out the PHYHD1 using CRISPR/Cas9, the chorion genes were significantly down-regulated. These results indicate that the silencing of PHYHD1 leads to the down-regulation of many chorion protein genes, which may be the direct cause of giant eggs. Overall design: To find mutant gene and explore the relationship between mutant gene and giant egg trait, the differentially expressed genes (DEGs) in the oviducts of Yun7 and Yun7Ge were analyzed by high-throughput sequencing, and two replicates were set for each sample.
Sample: GE2_oviducts of Yun7Ge
SAMN18942665 • SRS8814046 • All experiments • All runs
Organism: Bombyx mori
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was prepared using TRIzol (Invitrogen) from the mixture of three whole oviduct of Yun7 and Yun7Ge before mating, and two replicates were set for each sample. RNA degradation and contamination was monitored on 1% agarose gels. RNA purity was checked using the NanoPhotometer® spectrophotometer (IMPLEN, CA, USA). RNA concentration was measured using Qubit® RNA Assay Kit in Qubit®2.0 Flurometer (Life Technologies, CA, USA). RNA integrity was assessed using the RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). A total amount of 1.5 μg RNA per sample was used as input material for the RNA sample preparations. RNA libraries were prepared for sequencing using standard illumina protocols
Experiment attributes:
GEO Accession: GSM5273495
Links:
Runs: 1 run, 34.5M spots, 10.3G bases, 4.2Gb
Run# of Spots# of BasesSizePublished
SRR1437176234,499,16310.3G4.2Gb2021-05-03

ID:
14258244

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