The ADIPOQ gene-encoded adiponectin is a protein hormone produced exclusively by adipocytes (fat cells). It is transported through the bloodstream to muscle and liver cells. Adiponectin regulates various pathways related to fat storage and metabolism, including the modulation of blood glucose levels, fatty acid breakdown, brown adipocyte differentiation, and negative regulation of gluconeogenesis. By increasing insulin sensitivity and promoting fatty acid breakdown, adiponectin plays a crucial role in regulating glucose and fat metabolism. Additionally, it exhibits direct anti-diabetic, anti-atherosclerotic, and anti-inflammatory activities ^[1-2]. The mutation of the ADIPOQ gene is associated with adiponectin deficiency syndrome. Although the ADIPOQ gene is expressed predominantly (or almost exclusively) in adipose tissue, adiponectin, as a secreted hormone, circulates via the bloodstream and is widely distributed in various tissues and organs, including skeletal muscle, liver, intestine, male reproductive glands, and brain, where it exerts its physiological effects through specific receptors (such as AdipoR1 and AdipoR2) ^[3-4]. The Adipoq-iCre mice are constructed by inserting a codon-improved Cre recombinase (iCre) element into the endogenous Adipoq gene of mice. The expression pattern of iCre recombinase is similar to the endogenous gene. When this strain is crossed with mice containing loxP sites, sequence recombination mediated by the Cre recombinase between loxP sites can occur in the white adipose tissue (WAT) and brown adipose tissue (BAT) of its offspring.

Adiponectin, a protein hormone encoded by the ADIPOQ gene, is exclusively produced by adipocytes. It is secreted into the bloodstream and transported to muscle and liver cells, playing a crucial role in maintaining glucose and lipid metabolic homeostasis. Adiponectin participates in the regulation of glucose metabolism, lipolysis, and energy balance by promoting fatty acid oxidation, enhancing insulin sensitivity, and modulating metabolic signaling pathways such as AMPK. Additionally, it exhibits biological functions including anti-inflammatory and anti-atherosclerotic effects, as well as the amelioration of insulin resistance ^[1-3]. Aberrant ADIPOQ expression is closely associated with various metabolic disorders, including obesity, type 2 diabetes, metabolic syndrome, fatty liver disease, and cardiovascular diseases ^[1-4]. Although the ADIPOQ gene is expressed exclusively in adipose tissue, adiponectin is widely distributed across multiple organs, including muscle, liver, intestine, male reproductive glands, and the brain ^[3-4]. The Adipoq-P2A-iCreERT2 mouse was generated by inserting a P2A-iCreERT2 expression cassette at the stop codon of the endogenous mouse Adipoq gene. The regulatory elements of the mouse Adipoq gene drive the expression of the iCreERT2 recombinase. In the absence of tamoxifen, the iCreERT2 recombinase is predominantly retained in the cytoplasm; upon tamoxifen induction, the recombinase translocates into the nucleus to exert its recombinase activity. When Adipoq-P2A-iCreERT2 mice are crossed with mice carrying loxP sites, the resulting offspring are expected to undergo Cre-mediated recombination of sequences flanked by loxP sites within adipose tissue following tamoxifen induction.

Lpin3 is located on chromosome 2 of mice. Nuclease Technology was used to design sgRNA; Lpin3 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.

Adipoq is located on chromosome 16 of mice. Nuclease Technology will be used to design sgRNA; Adipoq knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.

Adipoq is located on chromosome 16 of mice. Nuclease Technology will be used to design sgRNA; Adipoq knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.

Adipoq is located on chromosome 16 of mice. Nuclease Technology was used to design sgRNA; Adipoq knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.

Adipoq is located on chromosome 16 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Adipoq conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.