1. Academic Validation
  2. Regulation of the Homeostasis of Early Embryo Development in Dairy Cows by Targeted Editing of the PRLR Gene-Mediated Activation of the Anti-Heat Stress Pathway

Regulation of the Homeostasis of Early Embryo Development in Dairy Cows by Targeted Editing of the PRLR Gene-Mediated Activation of the Anti-Heat Stress Pathway

  • Cells. 2025 Nov 25;14(23):1856. doi: 10.3390/cells14231856.
Xin Cheng 1 2 3 Daqing Wang 1 2 3 Xingyu Zhang 1 2 3 Lu Li 1 4 Yiyi Liu 1 4 Guifang Cao 1 2 3 5 Yong Zhang 1 2 3
Affiliations

Affiliations

  • 1 College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010011, China.
  • 2 Animal Embryo and Developmental Engineering Key Laboratory of Higher Education, Institutions of Inner Mongolia Autonomous Region, Hohhot 010011, China.
  • 3 Inner Mongolia Autonomous Region Key Laboratory of Basic Veterinary Medicine, Hohhot 010011, China.
  • 4 College of Life Sciences, Inner Mongolia Agricultural University, Hohhot 010011, China.
  • 5 College of Life Sciences, Inner Mongolia University, Hohhot 010021, China.
Abstract

The intensification of global climate warming exacerbates the issue of heat stress in dairy cows, making the SLICK mutation in the Prolactin receptor (PRLR) gene a critical target for enhancing heat tolerance in these Animals. This study aims to investigate the effects of CRISPR/Cas9-mediated editing of the PRLR gene on the biological characteristics of bovine fibroblasts and early embryonic development following somatic cell nuclear transfer (SCNT). Using the CRISPR/Cas9 system, we targeted and edited a 20 bp-150 bp region within exon nine of the PRLR gene. After conducting off-target predictions and activity screenings, we identified optimal guide RNA (sgRNA) sequences and established stable transgenic cell lines. Transcriptome Sequencing was performed on edited cells to identify key genes and validate their expression profiles. Edited cells were utilized as donor cells for SCNT, during which we assessed oocyte levels of Reactive Oxygen Species (ROS), glutathione (GSH), and mitochondrial function to analyze embryonic developmental performance. We constructed a cellular stress resistance network aimed at mitigating damage transmission while maintaining embryonic developmental homeostasis. This research provides technical support and theoretical reference for genetic editing breeding programs aimed at improving heat tolerance in dairy cattle.

Keywords

PRLR; differentially expressed genes; gene editing; key genes; somatic cell nuclear transfer; thermal stress.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-D0938
    98.23%, Cell Proliferation Fluorescent Probe