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KLF4通过直接靶向C/EBPβ抑制山羊肌内前体脂肪细胞的分化。

KLF4 Inhibits the Differentiation of Goat Intramuscular Preadipocytes Through Targeting C/EBPβ Directly.

作者信息

Xu Qing, Li Yanyan, Lin Sen, Wang Yong, Zhu Jiangjiang, Lin Yaqiu

机构信息

Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Ministry of Education, Southwest Minzu University, Chengdu, China.

Key Laboratory of Sichuan Province for Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Exploitation, Southwest Minzu University, Chengdu, China.

出版信息

Front Genet. 2021 Aug 4;12:663759. doi: 10.3389/fgene.2021.663759. eCollection 2021.

Abstract

Intramuscular fat (IMF) deposition is a complicated process, and most of the underlying regulators of this biological process are unknown. Here, we cloned the intact CDS of gene, investigated the role of KLF4 by gaining or losing function and further explored the pathways of KLF4 regulating differentiation of intramuscular preadipocytes in goat. Our results show that goat gene consists of 1,536 bp encoding a protein of 486 amino acids. The expression of KLF4 is higher in the lung while lower in the heart and muscle in goat. Knockdown of KLF4 mediated by siRNA technique significantly promotes intramuscular preadipocyte lipid accumulation and upregulates mRNA expression of adipogenic related genes including C/EBPα, C/EBPβ, and PPARγ cultured cells. Consistently, overexpression of KLF4 inhibits intramuscular adipocyte lipid accumulation and significantly downregulation gene expression of C/EBPβ, PPARγ, , and Pref-1. Further, we found that other members of KLFs were upregulated or downregulated after interference or overexpression of KLF4, including KLF2 and KLF5-7. We also found that C/EBPβ was a potential target of KLF4, because it had an opposite expression pattern with KLF4 during the differentiation of intramuscular preadipocytes and had putative binding sites of KLF4. The dual-luciferase reporter assay indicated that overexpression of KLF4 inhibited the transcriptional activity of C/EBPβ. These results demonstrate that KLF4 inhibits the differentiation of intramuscular preadipocytes in goat by targeting C/EBPβ.

摘要

肌内脂肪(IMF)沉积是一个复杂的过程,而这个生物学过程的大多数潜在调节因子尚不清楚。在这里,我们克隆了基因的完整编码区(CDS),通过功能获得或缺失研究了KLF4的作用,并进一步探索了KLF4调节山羊肌内前体脂肪细胞分化的途径。我们的结果表明,山羊基因由1536个碱基对组成,编码一个486个氨基酸的蛋白质。山羊体内KLF4在肺中的表达较高,而在心脏和肌肉中的表达较低。通过小干扰RNA(siRNA)技术介导的KLF4敲低显著促进肌内前体脂肪细胞脂质积累,并上调培养细胞中包括C/EBPα、C/EBPβ和PPARγ在内的成脂相关基因的mRNA表达。同样,KLF4的过表达抑制肌内脂肪细胞脂质积累,并显著下调C/EBPβ、PPARγ、和Pref-1的基因表达。此外,我们发现KLF家族的其他成员在KLF4干扰或过表达后上调或下调,包括KLF2和KLF5 - 7。我们还发现C/EBPβ是KLF4的一个潜在靶点,因为它在肌内前体脂肪细胞分化过程中与KLF4具有相反的表达模式,并且具有KLF4的假定结合位点。双荧光素酶报告基因检测表明,KLF4的过表达抑制了C/EBPβ的转录活性。这些结果表明,KLF4通过靶向C/EBPβ抑制山羊肌内前体脂肪细胞的分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/762a/8373462/cc73dd59de81/fgene-12-663759-g001.jpg

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