Wildman Benjamin J, Godfrey Tanner C, Rehan Mohammad, Chen Yuechuan, Afreen Lubana H, Hassan Quamarul
RNA Biology and Epigenetics Laboratory, Department of Oral and Maxillofacial Surgery, School of Dentistry, University of Alabama, Birmingham AL, 35294.
Curr Mol Biol Rep. 2019 Mar;5(1):55-64. doi: 10.1007/s40610-019-0115-4. Epub 2019 Jan 24.
PURPOSE OF REVIEW-: Precise and temporal expression of Runx2 and its regulatory transcriptional network is a key determinant for the intricate cellular and developmental processes in adult bone tissue formation. This review analyzes how microRNA functions to regulate this network, and how dysregulation results in bone disorders.
RECENT FINDINGS-: Similar to other biologic processes, microRNA (miRNA/miR) regulation is undeniably indispensable to bone synthesis and maintenance. There exists a miRNA-RUNX2 network where RUNX2 regulates the transcription of miRs, or is post transcriptionally regulated by a class of miRs, forming a variety of miR-RUNX2 regulatory pathways which regulate osteogenesis.
SUMMARY-: The current review provides insights to understand transcriptional-post transcriptional regulatory network governed by Runx2 and osteogenic miRs, and is based largely from in vitro and in vivo studies. When taken together, this article discusses a new regulatory layer of bone tissue specific gene expression by RUNX2 influenced via miRNA.
Runx2及其调控转录网络的精确和适时表达是成年骨组织形成中复杂细胞和发育过程的关键决定因素。本综述分析了微小RNA如何调控该网络,以及失调如何导致骨疾病。
与其他生物学过程类似,微小RNA(miRNA/miR)调控对于骨合成和维持无疑是不可或缺的。存在一个miRNA-RUNX2网络,其中RUNX2调控miR的转录,或在转录后受一类miR的调控,形成多种调控成骨的miR-RUNX2调控途径。
本综述提供了见解,以理解由Runx2和成骨miR控制的转录-转录后调控网络,并且很大程度上基于体外和体内研究。综上所述,本文讨论了由RUNX2通过miRNA影响的骨组织特异性基因表达的新调控层面。