Mouse models of obesity (ob/ob) and diabetes (db/db) in which the leptin (Lep) and leptin receptor (Lepr) genes have been mutated, respectively, have contributed to a better understanding of human obesity and type 2 diabetes and to the prevention, diagnosis, and treatment of these metabolic diseases. In this study, we report the first CRISPR-Cas9-induced Lep and Lepr knockout (KO) mouse models by co-microinjection of Cas9 mRNA and sgRNAs that specifically targeted Lep or Lepr in C57BL/6J embryos. Our newly established Lep and Lepr KO mouse models showed phenotypic disorders nearly identical to those found in ob/ob and db/db mice, such as an increase in body weight, hyperglycemia, and hepatic steatosis. Thus, Cas9-generated Lep and Lepr KO mouse lines will be easier for genotyping, to maintain the lines, and to use for future obesity and diabetes research.
Bibliographical noteFunding Information:
This work was supported by grants from the national
This work was supported by grants from the National Research Foundation of Korea (NRF) grants funded by the Korean government (MEST; 2010–0020878, 2012R1A1A2009607, 2015R1A2A1A01003845), the Ministry of Food and Drug Safety (14182MFDS978), a Korea Healthcare Technology R&D Project from the Ministry for Health and Welfare and Family Affairs (A085136) (to H-W Lee), the Ministry of Food and Drug Safety (14182MFDS978), and by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF-2016R1A2B4015866; to J-Y Cha).
© 2018 Japanese Association for Laboratory Animal Science.
All Science Journal Classification (ASJC) codes
- Animal Science and Zoology
- Biochemistry, Genetics and Molecular Biology(all)