Aksoy Mehmet Onur, Bilinska Adrianna, Stachowiak Monika, Flisikowska Tatiana, Szczerbal Izabela
Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Wolynska 33, 60-637 Poznan, Poland.
Chair of Livestock Biotechnology, School of Life Sciences, Technical University of Munich (TUM), D-85354 Freising, Germany.
Int J Mol Sci. 2024 Nov 26;25(23):12677. doi: 10.3390/ijms252312677.
Sterol regulatory element-binding protein 1 (SREBP1) is an important transcription factor that controls lipid metabolism and adipogenesis. Two isoforms, SREBP1a and SREBP1c, are generated by alternative splicing of the first exon of the gene. The porcine gene has mainly been studied for its role in lipid metabolism in adipose tissues, but little is known about its involvement, and the role of its two isoforms, in adipogenesis. The aim of the present study was to introduce a deletion in the 5'-regulatory region of the gene, considered crucial for adipogenesis, using the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated protein 9 (CRISPR/Cas9) method. This approach allows for the evaluation of how inhibiting transcription affects the expression of other genes essential for adipocyte differentiation, particularly , , , , , and . It was observed that disrupting the isoform had no effect on the gene but did result in a decrease in the expression of the and genes, an increase in the expression of , and an inhibition in the expression of the and genes. These changes in gene expression blocked adipogenesis, as could be seen by the failure of lipid droplets to accumulate. Our results provide evidence highlighting the pivotal role of the isoform in the regulation of porcine adipogenesis.
固醇调节元件结合蛋白1(SREBP1)是一种控制脂质代谢和脂肪生成的重要转录因子。该基因的第一个外显子通过可变剪接产生两种异构体,即SREBP1a和SREBP1c。猪的该基因主要因其在脂肪组织脂质代谢中的作用而被研究,但对于其在脂肪生成中的参与情况以及两种异构体的作用知之甚少。本研究的目的是使用成簇规律间隔短回文重复序列/CRISPR相关蛋白9(CRISPR/Cas9)方法,在该基因的5'调控区域引入一个缺失,该区域被认为对脂肪生成至关重要。这种方法能够评估抑制该基因转录如何影响脂肪细胞分化所必需的其他基因的表达,特别是、、、、和。观察到破坏该异构体对基因没有影响,但确实导致和基因的表达下降,基因的表达增加,以及和基因的表达受到抑制。基因表达的这些变化阻碍了脂肪生成,从脂滴未能积累可以看出这一点。我们的结果提供了证据,突出了该异构体在猪脂肪生成调控中的关键作用。