Departament de Ciència Animal i dels Aliments, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
J Dairy Sci. 2010 Sep;93(9):4332-9. doi: 10.3168/jds.2009-2597.
Genetic variability of the caprine stearoyl-CoA desaturase 1 (SCD1) gene has been investigated by sequencing a 4.7-kb cDNA in 6 goats from the Murciano-Granadina and Malagueña breeds. Sequence alignment revealed the existence of one synonymous polymorphism at exon 5 (c.732C>T) and one nucleotide substitution (c.*3504G>A) at exon 6 that encodes the 3' untranslated region (UTR). Moreover, the existence of a previously reported 3'UTR polymorphism involving a 3-bp indel (c.*1902_1904delTGT) was confirmed. Single nucleotide polymorphism and haplotype-based association analyses revealed suggestive associations between genetic variability of the SCD1 locus and lactose, stearic, polyunsaturated, and conjugated linoleic fatty acid contents. Associations with milk fatty acid composition might be explained by the global effects that SCD1 exerts on mammary gland lipid metabolism through the down-modulation of key transcription factors. Interestingly, the performance of an in silico analysis revealed that the c.*1902_1904delTGT polymorphism involves a considerable change in the secondary structure of the SCD1 mRNA. Gene reporter assays and quantitative PCR analysis would be needed to assess if this mutation has a causal effect on milk polyunsaturated and conjugated linoleic fatty acid levels by altering the amount of SCD1 transcripts in mammary epithelial cells.
本研究通过对来自穆尔西亚-格拉纳迪纳和马拉加纳品种的 6 只山羊的 4.7kb cDNA 进行测序,研究了山羊硬脂酰辅酶 A 去饱和酶 1(SCD1)基因的遗传变异性。序列比对揭示了外显子 5(c.732C>T)存在一个同义多态性,外显子 6 存在一个核苷酸取代(c.*3504G>A),该取代编码 3'非翻译区(UTR)。此外,还证实了先前报道的涉及 3'UTR 中 3 个碱基缺失(c.*1902_1904delTGT)的多态性。单核苷酸多态性和基于单倍型的关联分析显示,SCD1 基因座的遗传多态性与乳糖、硬脂酸、多不饱和脂肪酸和共轭亚油酸的含量存在关联。SCD1 通过下调关键转录因子对乳腺脂质代谢的全面影响,可能解释了与乳脂肪酸组成的关联。有趣的是,计算机分析显示,c.*1902_1904delTGT 多态性涉及 SCD1 mRNA 二级结构的显著变化。需要进行基因报告基因检测和定量 PCR 分析,以评估该突变是否通过改变乳腺上皮细胞中 SCD1 转录本的数量,对乳多不饱和和共轭亚油酸脂肪酸水平产生因果影响。