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High Expression of ZFP42 Improves Early Development of Pig Embryos Produced by Handmade Cloning.
Liu, Tianbin; Wu, Yan; Li, Lin; Zhang, Tingting; Zhang, Xingju; Li, Yong.
Affiliation
  • Liu T; Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Wu Y; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
  • Li L; Animal Breeding Department, BGI Institute of Applied Agriculture, Shenzhen, China.
  • Zhang T; BGI-Shenzhen, Shenzhen, China.
  • Zhang X; Animal Breeding Department, BGI Institute of Applied Agriculture, Shenzhen, China.
  • Li Y; BGI-Shenzhen, Shenzhen, China.
Cell Reprogram ; 26(2): 57-66, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38598277
ABSTRACT
Handmade Cloning (HMC) is a pivotal technique for cloning pig embryos. Despite its significance, the low efficiency of this method hampers its widespread application. Although numerous factors and signaling pathways influencing embryo development have been studied, the mechanisms underlying low developmental capacity and insufficient reprogramming of cloned embryos remain elusive. In the present study, we sought to elucidate key regulatory factors involved in the development of pig HMC embryos by comparing and analyzing the gene expression profiles of HMC embryos with those of naturally fertilized (NF) embryos at the 4-cell, 8-cell, and 16-cell stages. The results showed that ZFP42 expression is markedly higher in NF embryos than in cloned counterparts. Subsequent experiments involving the injection of ZFP42 messenger RNA (mRNA) into HMC embryos showed that ZFP42 could enhance the blastocyst formation rate, upregulate pluripotent genes and metabolic pathways. This highlights the potential of ZFP42 as a critical factor in improving the development of pig HMC embryos.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cloning, Organism / Nuclear Transfer Techniques Limits: Animals Language: En Journal: Cell Reprogram Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cloning, Organism / Nuclear Transfer Techniques Limits: Animals Language: En Journal: Cell Reprogram Year: 2024 Document type: Article Affiliation country: Country of publication: