Functional studies on methylation of the promoter region of the NR2E1 gene regulating adipocytes in beef cattle.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lan Feng, Xue Bai, Yuan Liu, Hongen Chu, Na Rina, Fen Li, Bei Cai, Dawei Wei, Runjun Yang, Lupei Zhang, Yun Ma
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引用次数: 0

Abstract

Background: Methylation plays a pivotal role in the modulation of gene expression, with the occurrence of promoter and exon 1 methylation typically resulting in transcriptional repression. Lipid deposition constitutes a complex economic trait, with a multitude of genes participating in the regulatory cascade that shapes meat quality attributes. Nonetheless, the available data on genetic markers for meat quality and the corresponding functional genes remains scarce, posing significant challenges to the selection of superior breeds and the development of novel strains in beef cattle breeding programs.

Results: In the present investigation, we evaluated the methylation profile of the NR2E1 gene within the promoter CpG islands across three distinct breeds of beef cattle, and elucidated its regulatory role in modulating the proliferation, differentiation, and apoptosis of adipocytes specifically in the Guyuan cattle breed. Subsequently, the functional validation of the NR2E1 gene was conducted in the predipocyte of Guyuan cattle. The results revealed an inverse correlation between the methylation level assessments and the RNA-seq data. Specifically, the mean methylation levels in 10 CpG islands situated within the promoter region of the NR2E1 gene were observed to be highest in Wagyu cattle, with Guyuan cattle exhibiting the subsequent highest levels, and the lowest in Chinese Simmental cattle. This methylation pattern exhibited a negative correlation with the RNA-seq outcomes. The interference with the NR2E1 gene repressed the proliferation and differentiation of bovine adipocytes by down-regulating the expression of both proliferation-associated genes and differentiation-related genes. Moreover, it potentially facilitated apoptosis in bovine adipocytes through up-regulating the pro-apoptotic gene BAD and down-regulating the apoptosis suppressor gene BCL2. Further downstream pathway analysis revealed that interference with the NR2E1 gene activated the AKT pathway, whereas its over expression led to the inhibition of this pathway.

Conclusions: In the present investigation, we conducted methylation sequencing of the CpG island within the promoter region of the NR2E1 in three breeds of beef cattle, followed by a comprehensive co-analysis with transcriptome data. We further explored the influence of the NR2E1 on the proliferation, differentiation, apoptosis, and downstream signaling pathways in bovine adipocytes. The findings of this research serve as a foundational reference for advancing the molecular understanding of NR2E1 regulation in the context of bovine adipocyte biology.

肉牛脂肪细胞调控基因NR2E1启动子区甲基化的功能研究。
背景:甲基化在基因表达调控中起着关键作用,启动子和外显子1甲基化的发生通常会导致转录抑制。脂质沉积是一种复杂的经济性状,有许多基因参与形成肉质属性的调控级联。然而,关于肉质遗传标记和相应功能基因的可用数据仍然很少,这对肉牛育种计划中优良品种的选择和新品系的开发构成了重大挑战。结果:在本研究中,我们评估了三种不同肉牛品种启动子CpG岛内NR2E1基因的甲基化谱,并阐明了其在固原牛品种中特异性调节脂肪细胞增殖、分化和凋亡的调控作用。随后,在固原牛的前体细胞中对NR2E1基因进行了功能验证。结果显示甲基化水平评估与RNA-seq数据之间呈负相关。具体而言,位于NR2E1基因启动子区域的10个CpG岛的平均甲基化水平在和牛中最高,固原牛次之,中国西门特牛最低。这种甲基化模式与RNA-seq结果呈负相关。干扰NR2E1基因通过下调增殖相关基因和分化相关基因的表达抑制牛脂肪细胞的增殖和分化。此外,它可能通过上调促凋亡基因BAD和下调凋亡抑制基因BCL2促进牛脂肪细胞凋亡。进一步的下游通路分析表明,干扰NR2E1基因激活AKT通路,而其过表达导致该通路被抑制。结论:在本研究中,我们对3个肉牛品种NR2E1启动子区域CpG岛进行了甲基化测序,并与转录组数据进行了全面的联合分析。我们进一步探讨了NR2E1对牛脂肪细胞增殖、分化、凋亡及下游信号通路的影响。本研究结果为进一步了解牛脂肪细胞生物学中NR2E1调控的分子机制提供了基础参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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