Assessing Regulation of ERG and its Target Proteins by ERG Isoform 8

IF 1.4 4区 综合性期刊 Q2 MULTIDISCIPLINARY SCIENCES Iranian Journal of Science and Technology, Transactions A: Science Pub Date : 2024-08-15 DOI:10.1007/s40995-024-01683-z
Rizwan Ullah Khan, Sidra Mumtaz, Muhammad Imran Sohail, Naila Malkani
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Abstract

Ets-related gene (ERG) is a key protein in vascular homeostasis. It has multiple isoforms. These isoforms have predominant nuclear localization except ERG isoform 8. This isoform can modify the nuclear localization of other isoforms and can down-regulate other isoforms. However, the mechanism of this regulation and its impact on ERG target proteins is still unclear. This study is designed to analyze the effects of ERG8 on functional aspects of other isoforms. For this purpose, the expressions of ERG3 target genes; VE-cad, sox4, cxcr4 were analyzed after ERG8 and ERG3 co-transfection. Increasing ERG8 to ERG3 ratios were transfected in 293-HEK cells. qPCR analysis was performed on total RNA extracted from transfected cells to evaluate the changes in expression of target genes. Results showed that ERG3 alone significantly increased the expression of these target genes (p˂0.05). However, the increasing concentrations of ERG8 progressively decreased the expression of the target genes significantly (p˂0.05). For in silico prediction of the nature of ERG3-ERG8 interaction, their three-dimensional models were built using I-TASSER and interaction was predicted using HADDOCK 2.4. HADDOCK scores show that ERG8 via its pointed (PNT) domain can interact with Ets domain of ERG3 (HADDOCK score; -28.956 +/- 15.881) as well as PNT domain (HADDOCK score; -4.426 +/- 7.770). Our results indicate that ERG8 affect the transcription factor activity of ERG3 by hindering its binding with the DNA either through PNT or Ets domain

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评估 ERG 异构体 8 对 ERG 及其靶蛋白的调控作用
Ets 相关基因(ERG)是血管稳态中的一种关键蛋白。它有多种异构体。除 ERG 同工酶 8 外,这些同工酶都主要定位于核内。该同工酶能改变其他同工酶的核定位,并能下调其他同工酶。然而,这种调控机制及其对ERG靶蛋白的影响仍不清楚。本研究旨在分析ERG8对其他同工酶功能方面的影响。为此,研究人员分析了 ERG8 和 ERG3 共转染后 ERG3 靶基因 VE-cad、sox4 和 cxcr4 的表达情况。对从转染细胞中提取的总 RNA 进行 qPCR 分析,以评估目标基因表达的变化。结果显示,单独使用 ERG3 能显著增加这些靶基因的表达(p˂0.05)。然而,ERG8浓度的增加会使目标基因的表达量明显降低(p˂0.05)。为了对ERG3-ERG8相互作用的性质进行硅预测,使用I-TASSER建立了它们的三维模型,并使用HADDOCK 2.4预测了相互作用。HADDOCK 评分显示,ERG8 可通过其尖(PNT)结构域与 ERG3 的 Ets 结构域(HADDOCK 评分;-28.956 +/- 15.881)以及 PNT 结构域(HADDOCK 评分;-4.426 +/- 7.770)相互作用。我们的结果表明,ERG8通过PNT或Ets结构域阻碍ERG3与DNA的结合,从而影响ERG3的转录因子活性。
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来源期刊
CiteScore
4.00
自引率
5.90%
发文量
122
审稿时长
>12 weeks
期刊介绍: The aim of this journal is to foster the growth of scientific research among Iranian scientists and to provide a medium which brings the fruits of their research to the attention of the world’s scientific community. The journal publishes original research findings – which may be theoretical, experimental or both - reviews, techniques, and comments spanning all subjects in the field of basic sciences, including Physics, Chemistry, Mathematics, Statistics, Biology and Earth Sciences
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