| Literature DB >> 28273380 |
Teng Ma1, Jingli Tao1, Minghui Yang1, Changjiu He1, Xiuzhi Tian1, Xiaosheng Zhang2, Jinlong Zhang2, Shoulong Deng3, Jianzhong Feng2, Zhenzhen Zhang1, Jing Wang1, Pengyun Ji1, Yukun Song1, Pingli He4, Hongbing Han1, Juncai Fu1, Zhengxing Lian1, Guoshi Liu1.
Abstract
Melatonin as a potent antioxidant exhibits important nutritional and medicinal values. To produce melatonin-enriched milk will benefit the consumers. In this study, a sheep bioreactor which generates melatonin-enriched milk has been successfully developed by the technology that combined CRISPR/Cas9 system and microinjection. The AANAT and ASMT were cloned from pineal gland of Dorper sheep (Ovis aries). The in vitro studies found that AANAT and ASMT were successfully transferred to the mammary epithelial cell lines and significantly increased melatonin production in the culture medium compared to the nontransgenic cell lines. In addition, the Cas9 mRNA, sgRNA, and the linearized vectors pBC1-AANAT and pBC1-ASMT were co-injected into the cytoplasm of pronuclear embryos which were implanted into ewes by oviducts transferring. Thirty-four transgenic sheep were generated with the transgenic positive rate being roughly 35% which were identified by Southern blot and sequencing. Seven carried transgenic AANAT, two carried ASMT, and 25 carried both of AANAT and ASMT genes. RT-PCR and Western blot demonstrated that the lambs expressed these genes in their mammary epithelial cells and these animals produced melatonin-enriched milk. This is the first report to show a functional AANAT and ASMT transgenic animal model which produce significantly high levels of melatonin milk compared to their wild-type counterparts. The advanced technologies used in the study laid a foundation for generating large transgenic livestock, for example, the cows, which can produce high level of melatonin milk.Entities:
Keywords: zzm321990zzm321990AANATzzm321990zzm321990; zzm321990zzm321990ASMTzzm321990zzm321990; CRISPR/Cas9; mammary gland bioreactor; melatonin; pronuclear microinjection; sheep
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Year: 2017 PMID: 28273380 DOI: 10.1111/jpi.12406
Source DB: PubMed Journal: J Pineal Res ISSN: 0742-3098 Impact factor: 13.007