National Engineering Research Center for Breeding Swine Industry, College of Animal Science, South China Agricultural University, Guangzhou, 510642, China.
Guangdong Provincial Key Laboratory of Agro-Animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou, 510642, China.
Transgenic Res. 2019 Aug;28(3-4):369-379. doi: 10.1007/s11248-019-00127-4. Epub 2019 Apr 29.
Omega-3 polyunsaturated fatty acids (n-3 PUFAs) are essential for the development and health of mammals, such as humans and livestock. n-3 PUFAs must be supplied by diet due to the absence of a key gene, namely, delta-15 desaturase (fat1), which is responsible for synthesizing n-3 PUFAs from a major type of n-6 PUFAs, linoleic acid (LA). To increase the dietary intake of n-3 PUFAs for humans, fat1-expressing transgenic (TG) livestock have been produced to provide n-3 PUFA-rich meats for humans. However, these TG livestock synthesized n-3 PUFAs from diet-derived, instead of endogenously produced, n-6 PUFAs because they still lack the delta-12 desaturase (fat2) gene for catalyzing conversion of internal oleic acid (OA) to LA. To fill the gap in the de novo n-3 PUFA biosynthesis pathway and to increase n-3 PUFA content in livestock, TG pigs co-expressing fat1-fat2 were generated in the present work. The OA content decreased in fat1-fat2 TG pigs, suggesting that OA was converted to LA by fat2 transgene-encoded delta-12 desaturase. The n-3 PUFA level was elevated, and the n-6/n-3 PUFA ratio dropped in fat1-fat2 TG pigs, revealing that fat1 transgene promoted the synthesis of n-3 PUFAs from n-6 analogs. The expression levels of fatty acid elongase-5 (ELOVL5) and fatty acid elongase-2 (ELOVL2), which are two key enzyme genes for PUFA synthesis, as well as their transcription factor peroxisome proliferator-activated receptor α, increased in fat1-fat2 TG pigs. Thus, the fat1 transgene enhanced n-3 PUFA synthesis by upregulating the expression of enzyme genes involved in the PUFA synthesis pathways. Overall, this study provided a new strategy to produce n-3 PUFA-rich meat for human consumption. The generated fat1-fat2 TG pigs can also serve as a large animal model for studying the roles of n-3 PUFAs in human development and health.
ω-3 多不饱和脂肪酸(n-3PUFAs)对人类和家畜等哺乳动物的发育和健康至关重要。n-3PUFAs 必须通过饮食来提供,因为缺乏一个关键基因,即 δ-15 去饱和酶(fat1),它负责将 n-6PUFAs 中的主要类型亚油酸(LA)合成 n-3PUFAs。为了增加人类对 n-3PUFAs 的饮食摄入,已经生产了表达 fat1 的转基因(TG)家畜,为人类提供富含 n-3PUFA 的肉类。然而,这些 TG 家畜从饮食中合成 n-3PUFAs,而不是内源性产生的 n-6PUFAs,因为它们仍然缺乏催化内部油酸(OA)转化为 LA 的 δ-12 去饱和酶(fat2)基因。为了填补从头合成 n-3PUFA 生物合成途径中的空白,并增加家畜中 n-3PUFA 的含量,本工作中生成了共表达 fat1-fat2 的 TG 猪。fat1-fat2TG 猪中的 OA 含量降低,表明 OA 被 fat2 转基因编码的 δ-12 去饱和酶转化为 LA。n-3PUFA 水平升高,n-6/n-3PUFA 比值下降,表明 fat1 转基因促进了 n-6 类似物合成 n-3PUFA。脂肪酸延长酶-5(ELOVL5)和脂肪酸延长酶-2(ELOVL2)的表达水平,这两个是 PUFA 合成的两个关键酶基因,以及它们的转录因子过氧化物酶体增殖物激活受体-α,在 fat1-fat2TG 猪中增加。因此,fat1 转基因通过上调参与 PUFA 合成途径的酶基因的表达来增强 n-3PUFA 合成。总的来说,本研究为生产富含 n-3PUFA 的肉类供人类食用提供了一种新策略。所产生的 fat1-fat2TG 猪也可以作为研究 n-3PUFA 在人类发育和健康中作用的大型动物模型。