Litcius/Paper detail

Targeted overexpression of PPARγ in skeletal muscle by random insertion and CRISPR/Cas9 transgenic pig cloning enhances oxidative fiber formation and intramuscular fat deposition

Hao Gu, Ying Zhou, Jinzeng Yang, Jianan Li, Yaxin Peng, Xia Zhang, Yi‐Liang Miao, Wei Jiang, Guowei Bu, Liming Hou, Ting Li, Lin Zhang, Xiaoliang Xia, Zhiyuan Ma, Yuanzhu Xiong, Bo Zuo

2021The FASEB Journal75 citationsDOIOpen Access PDF

Abstract

Abstract Peroxisome proliferator‐activated receptor gamma (PPARγ) is a master regulator of adipogenesis and lipogenesis. To understand its roles in fiber formation and fat deposition in skeletal muscle, we successfully generated muscle‐specific overexpression of PPARγ in two pig models by random insertion and CRISPR/Cas9 transgenic cloning procedures. The content of intramuscular fat was significantly increased in PPARγ pigs while had no changes on lean meat ratio. PPARγ could promote adipocyte differentiation by activating adipocyte differentiating regulators such as FABP4 and CCAAT/enhancer‐binding protein (C/EBP), along with enhanced expression of LPL, FABP4, and PLIN1 to proceed fat deposition. Proteomics analyses demonstrated that oxidative metabolism of fatty acids and respiratory chain were activated in PPARγ pigs, thus, gathered more Ca 2+ in PPARγ pigs. Raising of Ca 2+ could result in increased phosphorylation of CAMKII and p38 MAPK in PPARγ pigs, which can stimulate MEF2 and PGC1α to affect fiber type and oxidative capacity. These results support that skeletal muscle‐specific overexpression of PPARγ can promote oxidative fiber formation and intramuscular fat deposition in pigs.

Topics & Concepts

Intramuscular fatPeroxisome proliferator-activated receptorLipogenesisEndocrinologyInternal medicineAdipogenesisSkeletal muscleBiologyAdipocyteTransgeneCell biologyLipid metabolismChemistryAdipose tissueReceptorBiochemistryMedicineGeneAdipose Tissue and MetabolismPeroxisome Proliferator-Activated ReceptorsAdipokines, Inflammation, and Metabolic Diseases