Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan 16:11:1097780.
doi: 10.3389/fcell.2023.1097780. eCollection 2023.

The dynamics of chromatin states mediated by epigenetic modifications during somatic cell reprogramming

Affiliations
Review

The dynamics of chromatin states mediated by epigenetic modifications during somatic cell reprogramming

Jing Peng et al. Front Cell Dev Biol. .

Abstract

Somatic cell reprogramming (SCR) is the conversion of differentiated somatic cells into totipotent or pluripotent cells through a variety of methods. Somatic cell reprogramming also provides a platform to investigate the role of chromatin-based factors in establishing and maintaining totipotency or pluripotency, since high expression of totipotency- or pluripotency-related genes usually require an active chromatin state. Several studies in plants or mammals have recently shed light on the molecular mechanisms by which epigenetic modifications regulate the expression of totipotency or pluripotency genes by altering their chromatin states. In this review, we present a comprehensive overview of the dynamic changes in epigenetic modifications and chromatin states during reprogramming from somatic cells to totipotent or pluripotent cells. In addition, we illustrate the potential role of DNA methylation, histone modifications, histone variants, and chromatin remodeling during somatic cell reprogramming, which will pave the way to developing reliable strategies for efficient cellular reprogramming.

Keywords: cell pluripotency; cell totipotency; chromatin state; epigenetic modification; gene expression; somatic cell reprogramming.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
An overview of epigenetic factors dynamically regulating the chromatin state during somatic cell reprogramming. The diagrams illustrate the reprogramming of somatic cells to pluripotent or totipotent cells along with the associated epigenetic modifications in plants (A) and mammals (B). DNA methylation acts as a barrier during SCR in both mammals and plants. Most pluripotency or totipotency genes are hypermethylated and transcriptionally silenced in somatic cells, and they are (re) activated through active DNA demethylation during SCR. Histone methylation is also required for SCR. Different histone methylation marks induce open or repressive chromatin states, ensuring the activation of pluripotency or totipotency genes to promote SCR. Histone acetylation acts as an epigenetic activator of reprogramming by establishing a chromatin structure that promotes the activation of a transcriptional network that regulates pluripotency or totipotency. Histone variants and chromatin remodeling are also associated with histone modifications and impose a repressive chromatin state to prevent the reactivation of critical pluripotency or totipotency genes during SCR.

Similar articles

Cited by

References

    1. Aichinger E., Villar C. B., Farrona S., Reyes J. C., Hennig L., Kohler C. (2009). CHD3 proteins and polycomb group proteins antagonistically determine cell identity in Arabidopsis. PLoS Genet. 5 (8), e1000605. 10.1371/journal.pgen.1000605 - DOI - PMC - PubMed
    1. Allis T. J. C. D., Allis C. D. (2001). Translating the histone code. Science 293 (5532), 1074–1080. 10.1126/science.1063127 - DOI - PubMed
    1. Ang Y., Tsai S., Lee D. F., Monk J. M., Su J., Ratnakumar K., et al. (2011). Wdr5 mediates self-renewal and reprogramming via the embryonic stem cell core transcriptional network. Cell. 145 (2), 183–197. 10.1016/j.cell.2011.03.003 - DOI - PMC - PubMed
    1. Anzola J. M., Sieberer T., Ortbauer M., Butt H., Korbei B., Weinhofer I., et al. (2010). Putative Arabidopsis transcriptional adaptor protein (PROPORZ1) is required to modulate histone acetylation in response to auxin. Proc. Natl. Acad. Sci. U. S. A. 107 (22), 10308–10313. 10.1073/pnas.0913918107 - DOI - PMC - PubMed
    1. Bannister A. J, S. R., Kouzarides T. (2002). Histone methylation: Dynamic or static? Cell. 109 (7), 801–806. 10.1016/S0092-8674(02)00798-5 - DOI - PubMed

Grants and funding

This work was funded by the National Natural Science Foundation of China (31872669, 32070199) and the Program for Scientific Research Innovation Team of Young Scholar in Colleges and Universities of Shandong Province (2019KJE011).

LinkOut - more resources