2022
DOI: 10.3389/fcell.2022.958205
|View full text |Cite
|
Sign up to set email alerts
|

The transcriptome landscapes of allantochorion and vitelline-chorion in equine day 30 conceptus

Abstract: During equine early gestation, trophectoderm forms chorion tissue, which is composed of two parts that one is covering allantoin, called allantochorion (AC) and another is covering yolk sac, which here we call vitelline-chorion (VC). Given that little is known about the equine trophoblast-derived chorion differentiation at an early stage, we first compared the transcriptome of AC and VC of day 30 equine conceptus based on RNA-sequencing. As a result, we found that compared to VC, there are 484 DEGs, including … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

1
0

Authors

Journals

citations
Cited by 1 publication
(2 citation statements)
references
References 52 publications
0
2
0
Order By: Relevance
“…Nine genes (CYP11A1, CYP17A1, HSD17B7, LDLR, SCARB1, STAR, PLA1A, CPNE5 and COL4A4) that were found to be differentially expressed were selected for qPCR validation. Total RNA isolation, cDNA synthesis and qPCR analysis were conducted as previously described (Shen et al., 2022). The primers used for qPCR analysis are listed in Table S1, with GAPDH identified as a reference control.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Nine genes (CYP11A1, CYP17A1, HSD17B7, LDLR, SCARB1, STAR, PLA1A, CPNE5 and COL4A4) that were found to be differentially expressed were selected for qPCR validation. Total RNA isolation, cDNA synthesis and qPCR analysis were conducted as previously described (Shen et al., 2022). The primers used for qPCR analysis are listed in Table S1, with GAPDH identified as a reference control.…”
Section: Methodsmentioning
confidence: 99%
“…The qPCRs were performed on the Bio‐Rad CFX96 Real‐Time PCR System (Bio‐Rad, USA) using SYBR Green qPCR Mix (Takara, CHN) according to the manufacturer's instructions. The thermal cycling conditions were as follows: 95°C for 5 min, followed by 35 cycles of 95°C for 1 min and 60°C for 30 s. Relative gene expression levels were calculated using the 2ΔΔCt$$ {2}^{-\Delta \Delta {C}_t} $$ method (Shen et al., 2022).…”
Section: Methodsmentioning
confidence: 99%