Suresh Bharathi, Lee Junwon, Kim Kye-Seong, Ramakrishna Suresh
Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul 133-791, Republic of Korea.
Department of Physiology and Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Republic of Korea.
Stem Cells Int. 2016;2016:6705927. doi: 10.1155/2016/6705927. Epub 2016 Jan 6.
Ubiquitination of core stem cell transcription factors can directly affect stem cell maintenance and differentiation. Ubiquitination and deubiquitination must occur in a timely and well-coordinated manner to regulate the protein turnover of several stemness related proteins, resulting in optimal embryonic stem cell maintenance and differentiation. There are two switches: an E3 ubiquitin ligase enzyme that tags ubiquitin molecules to the target proteins for proteolysis and a second enzyme, the deubiquitinating enzyme (DUBs), that performs the opposite action, thereby preventing proteolysis. In order to maintain stemness and to allow for efficient differentiation, both ubiquitination and deubiquitination molecular switches must operate properly in a balanced manner. In this review, we have summarized the importance of the ubiquitination of core stem cell transcription factors, such as Oct3/4, c-Myc, Sox2, Klf4, Nanog, and LIN28, during cellular reprogramming. Furthermore, we emphasize the role of DUBs in regulating core stem cell transcriptional factors and their function in stem cell maintenance and differentiation. We also discuss the possibility of using DUBs, along with core transcription factors, to efficiently generate induced pluripotent stem cells. Our review provides a relatively new understanding regarding the importance of ubiquitination/deubiquitination of stem cell transcription factors for efficient cellular reprogramming.
核心干细胞转录因子的泛素化可直接影响干细胞的维持和分化。泛素化和去泛素化必须及时且协调良好地发生,以调节几种与干性相关蛋白质的蛋白质周转,从而实现胚胎干细胞的最佳维持和分化。存在两种开关:一种是E3泛素连接酶,它将泛素分子标记到靶蛋白上以便进行蛋白水解;另一种酶是去泛素化酶(DUBs),其作用相反,从而防止蛋白水解。为了维持干性并实现高效分化,泛素化和去泛素化这两种分子开关都必须以平衡的方式正常运作。在本综述中,我们总结了核心干细胞转录因子(如Oct3/4、c-Myc、Sox2、Klf4、Nanog和LIN28)在细胞重编程过程中泛素化的重要性。此外,我们强调了去泛素化酶在调节核心干细胞转录因子中的作用及其在干细胞维持和分化中的功能。我们还讨论了将去泛素化酶与核心转录因子一起使用以高效生成诱导多能干细胞的可能性。我们的综述为干细胞转录因子的泛素化/去泛素化对高效细胞重编程的重要性提供了一个相对新颖的认识。