肌内脂肪
生物
脂肪细胞
油红O
单核苷酸多态性
白细胞介素
脂肪生成
基因型
分子生物学
内分泌学
内科学
脂肪组织
细胞因子
遗传学
生物化学
基因
医学
作者
Danni He,Zheng Jiang,Ye Tian,Hui Han,Min Xia,Wei Wei,Lin Zhang,Junkai Chen
摘要
Summary Intramuscular fat ( IMF ) content is a key aspect of pork quality. Elucidation of intramuscular adipocyte regulation mechanisms is important for improving IMF content. Intramuscular adipocytes are dispersed among muscle fibers, so they are inclined to be affected by muscle‐derived factors. Interleukin‐15 is a major muscle‐secreted factor. In this study, the genetic and physiological impacts of IL 15 on adipogenesis is investigated. The promoter region of IL 15 was scanned by comparative sequencing using two DNA pools of high‐ and low‐ IMF individuals. Two SNP s, c.–342C>T (ss2137497757) and c.–334G>A (ss2137497756) (the translation start site is designated as +1), were identified with reverse allele distribution in these two groups. Genotyping by allele‐specific PCR revealed that the two SNP s were completely linked. The IMF content of TA/TA individuals was lower than that for CG/CG ones, whereas the IL 15 expression level was higher in T‐A/T‐A individuals. Luciferase assaying also revealed that the T‐A haplotype promoter had higher transcription activity. Meanwhile, the effect of interleukin‐15 on adipocyte differentiation was further assessed in vitro . Results showed that interleukin‐15 suppressed preadipocyte proliferation in a dose‐dependent manner. The cell cycle of preadipocytes was arrested, and apoptosis was induced. Oil Red O staining and triglyceride quantification indicated that adipocyte differentiation was also inhibited by interleukin‐15. The mRNA levels of PPARG and FABP 4 decreased markably upon interleukin‐15 treatment. Taken together, we identified two completely linked SNP s in the porcine IL 15 promoter region that could alter IL 15 transcription activity. As interleukin‐15 can inhibit porcine adipocyte differentiation, these promoter mutations could affect IMF deposition by producing differential levels of muscle‐derived interleukin‐15.
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