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MKRN2 基因敲除通过降低 STAT1、SIX4 和 TNC 的表达导致男性不育。

MKRN2 knockout causes male infertility through decreasing STAT1, SIX4, and TNC expression.

机构信息

The First Affiliated Hospital of Zhengzhou University, Academy of Medical Science, Zhengzhou University, Zhengzhou, Henan, China.

The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Front Endocrinol (Lausanne). 2023 Mar 10;14:1138096. doi: 10.3389/fendo.2023.1138096. eCollection 2023.

Abstract

() is an evolutionarily conserved gene whose biological functions are not fully known. Although recent studies have shed insights on the potential causes of male infertility, its underlining mechanisms still remain to be elucidated. We developed a knockout mice model to study this gene and found that deletion of in mice led to male infertility. Interestingly, the expression level of signal transducer and activator of the transcription (STAT)1 was significantly decreased in MKRN2 knockout testis and MEF cells. Co-IP assay showed an interaction between MKRN2 and STAT1. Moreover, our results further indicated that MKRN2 regulated the expression level of SIX4 and tenascin C (TNC) the EBF transcription factor 2 (EBF2) in mice. The results of our study will provide insights into a new mechanism of male infertility.

摘要

() 是一个进化上保守的基因,其生物学功能尚未完全阐明。尽管最近的研究揭示了导致男性不育的潜在原因,但它的潜在机制仍有待阐明。我们构建了 MKRN2 敲除小鼠模型来研究这个基因,发现 MKRN2 缺失导致了雄性不育。有趣的是,MKRN2 敲除睾丸和 MEF 细胞中信号转导和转录激活因子 (STAT)1 的表达水平显著降低。Co-IP 实验表明 MKRN2 和 STAT1 之间存在相互作用。此外,我们的结果还表明 MKRN2 调节了 SIX4 和腱生蛋白 C(TNC)以及 EBF 转录因子 2(EBF2)在小鼠中的表达水平。本研究的结果将为男性不育的新机制提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e801/10036822/20db8d8c9e74/fendo-14-1138096-g001.jpg

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