The autophagy initiation factor ATG13 mRNA is stabilized by the RNA-binding protein YBX3.

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Liva Pfuhler, Silina Awad, William Skipper, Jeremy Lavietes, Thomas Sah, Kayla Ho, Radha Ivanova, Amy Cooke
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引用次数: 0

Abstract

Autophagy, a highly conserved form of cellular recycling, is essential for cellular homeostasis. Its dysregulation has been linked to neurodegenerative diseases and various cancers, including breast cancer. We set out to determine if the RNA-binding protein (RBP) YBX3 regulates autophagy mRNAs, as previous findings suggest YBX3 depletion reduces distinct autophagy transcripts. We found that YBX3 interacts with and stabilizes the mRNA of the autophagy initiation factor ATG13 in HeLa, which in turn increases ATG13 protein expression. We have shown that this requires the 3' untranslated region (UTR) of ATG13 and occurs in other human cell lines, including HEK293, HepG2, and HCT116. Together, our data suggest a novel regulatory role for YBX3 of autophagy initiation through posttranscriptional control of ATG13 mRNA stability.

自噬启动因子 ATG13 mRNA 由 RNA 结合蛋白 YBX3 稳定。
自噬是一种高度保守的细胞循环形式,对细胞的平衡至关重要。它的失调与神经退行性疾病和包括乳腺癌在内的各种癌症有关。以前的研究结果表明,YBX3 的缺失会减少不同的自噬转录本,因此我们开始研究 RNA 结合蛋白(RBP)YBX3 是否调控自噬 mRNA。我们发现,YBX3 与 HeLa 中自噬启动因子 ATG13 的 mRNA 相互作用并使其稳定,进而增加 ATG13 蛋白的表达。我们的研究表明,这需要 ATG13 的 3' 非翻译区 (UTR),并发生在其他人类细胞系中,包括 HEK293、HepG2 和 HCT116。总之,我们的数据表明,YBX3 通过转录后控制 ATG13 mRNA 的稳定性,对自噬的启动起到了新的调控作用。
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
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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