Post-translational modification control of RNA-binding protein hnRNPK function. Issue 3 (6th March 2019)

• Record Type: Journal Article
• Authors: Xu, Yongjie; Wu, Wei; Han, Qiu; Wang, Yaling; Li, Cencen; Zhang, Pengpeng; Xu, Haixia
• Is Part Of: Open biology. Volume 9:Issue 3(2019)
• Publication Date: 2019-03-06
• Subjects: hnRNPK -- post-translational modifications -- phosphorylation -- methylation -- ubiquitination -- glycosylation; Biology -- Periodicals; 570
• DOI: 10.1098/rsob.180239
• Languages: English
• ISSNs: 2046-2441

Abstract

Abstract : Heterogeneous nuclear ribonucleoprotein K (hnRNPK), a ubiquitously occurring RNA-binding protein (RBP), can interact with numerous nucleic acids and various proteins and is involved in a number of cellular functions including transcription, translation, splicing, chromatin remodelling, etc. Through its abundant biological functions, hnRNPK has been implicated in cellular events including proliferation, differentiation, apoptosis, DNA damage repair and the stress and immune responses. Thus, it is critical to understand the mechanism of hnRNPK regulation and its downstream effects on cancer and other diseases. A number of recent studies have highlighted that several post-translational modifications (PTMs) possibly play an important role in modulating hnRNPK function. Phosphorylation is the most widely occurring PTM in hnRNPK. For example, in vivo analyses of sites such as S116 and S284 illustrate the purpose of PTM of hnRNPK in altering its subcellular localization and its ability to bind target nucleic acids or proteins. Other PTMs such as methylation, ubiquitination, sumoylation, glycosylation and proteolytic cleavage are increasingly implicated in the regulation of DNA repair, cellular stresses and tumour growth. In this review, we describe the PTMs that impact upon hnRNPK function on gene expression programmes and different disease states. This knowledge is key in allowing us to better understand the mechanism of hnRNPK regulation.