Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China; Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming, Yunnan 650204, China.
Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China; Department of Hepatobiliary Surgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China.
Biochim Biophys Acta Mol Cell Biol Lipids. 2018 Mar;1863(3):235-246. doi: 10.1016/j.bbalip.2017.12.007. Epub 2017 Dec 10.
Unsaturated fatty acids (UFAs) play crucial roles in living organisms regarding development, energy metabolism, stress resistance, etc. The biosynthesis of UFAs starts from the introduction of the first double bond by stearoyl-CoA desaturase (SCD), converting saturated fatty acids (SFAs) to monounsaturated fatty acids (MUFAs). This desaturation is considered to be an aerobic process that requires cytochrome b5 reductase, cytochrome b5 and SCD. However, this enzyme system remains elusive in Caenorhabditis elegans. Here, we show that inactivation by RNAi knockdown or mutation (gk442189) of putative cytochrome b5 genes cytb-5.1 led to reduced conversion of C18:0 to C18:1(n-9) by SCD desaturases FAT-6/7 in C. elegans. On the contrary, cytb-5.2RNAi and cytb-5.2(gk113588) mutant worms showed decreased conversion of C16:0 to C16:1(n-7) by FAT-5 desaturase. Dietary supplementation with C18:1(n-9) and C18:2(n-6) also showed that CYTB-5.1 is likely required for the activity of FAT-6/7 desaturases, but not for FAT-1 to FAT-4 desaturases. Interestingly, co-immunoprecipitation (Co-IP) demonstrated that either FAT-7 or FAT-5 has ability to interact with both CYTB-5.1 and CYTB-5.2. Moreover, RNAi knockdown of cytb-5.1 upregulates the transcriptional and translational expression of fat-5 to fat-7, which may be due to the feedback induction by reduced C18:1(n-9) and downstream fatty acids. Furthermore, both CYTB-5.1 and CYTB-5.2 are involved in fat accumulation, fertility and lifespan in worms, which may be independent of changes in fatty acid compositions. Collectively, these findings for the first time reveal the differential regulation of various SCDs by distinct cytochrome b5 CYTB-5.1 and CYTB-5.2 in the biosynthesis of UFAs in C. elegans.
不饱和脂肪酸 (UFAs) 在生物体内的发育、能量代谢、应激抵抗等方面发挥着至关重要的作用。UFAs 的生物合成始于硬脂酰辅酶 A 去饱和酶 (SCD) 将第一个双键引入饱和脂肪酸 (SFAs) 中,将其转化为单不饱和脂肪酸 (MUFAs)。这种去饱和作用被认为是一种需氧过程,需要细胞色素 b5 还原酶、细胞色素 b5 和 SCD。然而,这种酶系统在秀丽隐杆线虫中仍然难以捉摸。在这里,我们通过 RNAi 敲低或突变 (gk442189) 失活假定的细胞色素 b5 基因 cytb-5.1,发现这会导致 SCD 去饱和酶 FAT-6/7 对 C. elegans 中 C18:0 到 C18:1(n-9)的转化减少。相反,cytb-5.2RNAi 和 cytb-5.2(gk113588) 突变体蠕虫中 FAT-5 去饱和酶对 C16:0 到 C16:1(n-7)的转化减少。膳食补充 C18:1(n-9) 和 C18:2(n-6) 也表明,CYTB-5.1 可能是 FAT-6/7 去饱和酶活性所必需的,但不是 FAT-1 到 FAT-4 去饱和酶活性所必需的。有趣的是,共免疫沉淀 (Co-IP) 表明 FAT-7 或 FAT-5 都有能力与 CYTB-5.1 和 CYTB-5.2 相互作用。此外,cytb-5.1 的 RNAi 敲低会上调 fat-5 到 fat-7 的转录和翻译表达,这可能是由于减少的 C18:1(n-9) 和下游脂肪酸的反馈诱导。此外,CYTB-5.1 和 CYTB-5.2 都参与了线虫中脂肪的积累、繁殖和寿命,这可能与脂肪酸组成的变化无关。总的来说,这些发现首次揭示了在 C. elegans 的 UFAs 生物合成中,不同的细胞色素 b5 CYTB-5.1 和 CYTB-5.2 对各种 SCD 的差异调节。