“…With regard to livestock and poultry, some circRNAs have also been identified by high throughput sequencing and confirmed to participate in regulating their important biological process, such as embryos development ( Veno et al, 2015 ), formation of skeletal muscle fiber ( Li et al, 2020b ), hepatic lipid metabolism ( Huang et al, 2018 ), and adipogenic differentiation ( Li A. et al, 2018 ) in pig; muscle growth and development ( Wei et al, 2017 ; Li et al, 2018b ; Li et al, 2018c ; Liu et al, 2020 ; Shen et al, 2020 ; Yue et al, 2020 ; Elnour et al, 2021 ), testis development ( Gao et al, 2018 ), adipogenesis ( Jiang et al, 2020 ) and milk fat content ( Chen et al, 2021 ) in cattle; fat deposition in buffalo and yak ( Huang et al, 2019 ; Wang H. et al, 2020 ); intramuscular fat (IMF) content denoting a crucial indicator of meat quality in donkey ( Li et al, 2020a ); follicular development ( Shen et al, 2019 ), Marek’s tumourigenesis ( Wang L. et al, 2020 ) as well as muscle growth development ( Ouyang et al, 2018a ; Ouyang et al, 2018b ) in chicken. And it has yet indicated some functional circRNAs related to lipid metabolism, for instance, circFUT10 could promote bovine preadipocyte proliferation but inhibit adipocyte differentiation ( Jiang et al, 2020 ); circRNA_26852 and circRNA_11897, might get involved in porcine adipocyte differentiation and lipid metabolism ( Li A. et al, 2018 ); circ11103 could increase the triglyceride levels in bovine mammary epithelial cells and the contents of unsaturated fatty acids ( Chen et al, 2021 ); additionally, 19:45387150|45389986 and 21:6969877|69753491, were deemed as potential modulators of buffalo back subcutaneous adipose deposition ( Huang et al, 2019 ).…”