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猪比较基因鉴定-58(CGI-58)mRNA 的可变剪接及发育和激素调控。

Alternative splicing and developmental and hormonal regulation of porcine comparative gene identification-58 (CGI-58) mRNA.

机构信息

Department of Animal Sciences, The Ohio State University, Columbus 43210, USA.

出版信息

J Anim Sci. 2012 Dec;90(12):4346-54. doi: 10.2527/jas.2012-5151. Epub 2012 Jul 24.

Abstract

The process of lipolysis is essential for regulating the catabolism of cellular fat stores. Therefore, knowledge of lipolysis contributes to improving porcine production, such as reducing back fat, enhancing lean meat, and controlling marbling. Comparative gene identification-58 (CGI-58) plays an important role in the multi-enzyme-mediated process of lipolysis. It was identified as the co-activator of adipose triglyceride lipase (ATGL), which performs the first step in breaking down triacylglycerol and generating diacylglycerol and NEFA. We cloned and sequenced the CGI-58 cDNA and deduced the AA sequences in 3 breeds of swine (Duroc, Berkshire, and Landrace). Homologies were found with the human, mouse, and chicken for the lipid droplet binding domain, the α/β hydrolase domain, and the lysophosphatidic acid acyltransferase (LPAAT) domain, which demonstrates conservation of CGI-58 across species. An alternatively spliced isoform with an exon 3 deletion was identified. Interestingly, this unique isoform contains the lipid droplet-binding domain but lacks the LPAAT domain due to an open reading frame (ORF) shift that creates a premature stop codon. Furthermore, porcine CGI-58 is expressed in multiple organs and tissues but is most predominant in adipose tissue. Porcine adipose and stromal-vascular (SV) cell fractionation reveals that CGI-58 and ATGL are highly expressed (P < 0.01) in mature adipocytes. The expressions of both CGI-58 and ATGL mRNA were found to increase (P < 0.05) at d 6 of SV cell culture, confirming their upregulation during adipogenesis and differentiation. Also, the results from in vitro cell culture showed that insulin decreased (P < 0.05) the expressions of both CGI-58 and ATGL in a dose-dependent manner. Overall, these results report the cDNA and AA sequences of porcine CGI-58 with identification of its unique alternatively spliced variant. The results of the study also reveal the developmental and hormonal regulation of porcine CGI-58 gene, which contributes to the understanding of the role of CGI-58 in lipid metabolism. These findings suggest that CGI-58 may be a new target for enhancing the quality of pork products as well as offering the potential of CGI-58 for human obesity treatment.

摘要

脂肪分解的过程对于调节细胞脂肪储存的分解代谢至关重要。因此,对脂肪分解的了解有助于提高猪的生产性能,例如减少背部脂肪、增加瘦肉量和控制大理石纹。比较基因鉴定-58(CGI-58)在多酶介导的脂肪分解过程中发挥重要作用。它被鉴定为脂肪甘油三酯酶(ATGL)的共激活剂,ATGL 进行了第一步分解甘油三酯并生成二酰基甘油和非酯化脂肪酸。我们克隆和测序了 CGI-58 cDNA,并推导出了 3 个猪品种(杜洛克、伯克夏和长白猪)的 AA 序列。与人、鼠和鸡的同源性存在于脂滴结合结构域、α/β水解酶结构域和溶血磷脂酸酰基转移酶(LPAAT)结构域中,这表明 CGI-58 在物种间具有保守性。鉴定出一种具有外显子 3 缺失的选择性剪接异构体。有趣的是,这种独特的异构体含有脂滴结合结构域,但由于开放阅读框(ORF)移位导致提前终止密码子而缺乏 LPAAT 结构域。此外,猪 CGI-58 在多种器官和组织中表达,但在脂肪组织中表达最丰富。猪脂肪和基质血管(SV)细胞分离显示,CGI-58 和 ATGL 在成熟脂肪细胞中高度表达(P < 0.01)。SV 细胞培养第 6 天发现 CGI-58 和 ATGL mRNA 的表达均增加(P < 0.05),证实了它们在脂肪生成和分化过程中的上调。此外,体外细胞培养结果表明,胰岛素以剂量依赖的方式降低(P < 0.05) CGI-58 和 ATGL 的表达。总的来说,这些结果报告了猪 CGI-58 的 cDNA 和 AA 序列,并鉴定了其独特的选择性剪接变体。该研究结果还揭示了猪 CGI-58 基因的发育和激素调节,有助于了解 CGI-58 在脂质代谢中的作用。这些发现表明,CGI-58 可能成为提高猪肉产品质量的新靶点,并为 CGI-58 治疗人类肥胖提供潜力。

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