» Articles » PMID: 34616726

Advances in Chromodomain Helicase DNA-Binding (CHD) Proteins Regulating Stem Cell Differentiation and Human Diseases

Overview
Specialty Cell Biology
Date 2021 Oct 7
PMID 34616726
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Regulation of gene expression is critical for stem cell differentiation, tissue development, and human health maintenance. Recently, epigenetic modifications of histone and chromatin remodeling have been verified as key controllers of gene expression and human diseases. In this study, we review the role of chromodomain helicase DNA-binding (CHD) proteins in stem cell differentiation, cell fate decision, and several known human developmental disorders and cancers. CHD proteins play a crucial role in stem cell differentiation and human diseases.

Citing Articles

Epigenetic regulation in metabolic diseases: mechanisms and advances in clinical study.

Wu Y, Lin Z, Li C, Lin X, Shan S, Guo B Signal Transduct Target Ther. 2023; 8(1):98.

PMID: 36864020 PMC: 9981733. DOI: 10.1038/s41392-023-01333-7.


CHD1, a multifaceted epigenetic remodeler in prostate cancer.

Li H, Gigi L, Zhao D Front Oncol. 2023; 13:1123362.

PMID: 36776288 PMC: 9909554. DOI: 10.3389/fonc.2023.1123362.


Discovery of Novel Variants on the Gene: A Case Series of CHARGE Syndrome.

Wu X, Chen L, Lu W, He S, Li X, Sun L Front Genet. 2022; 13:852429.

PMID: 35938004 PMC: 9355507. DOI: 10.3389/fgene.2022.852429.


CHD Chromatin Remodeling Protein Diversification Yields Novel Clades and Domains Absent in Classic Model Organisms.

Trujillo J, Long J, Aboelnour E, Ogas J, Wisecaver J Genome Biol Evol. 2022; 14(5).

PMID: 35524943 PMC: 9113485. DOI: 10.1093/gbe/evac066.


CHD7 regulates bone-fat balance by suppressing PPAR-γ signaling.

Liu C, Xiong Q, Li Q, Lin W, Jiang S, Zhang D Nat Commun. 2022; 13(1):1989.

PMID: 35418650 PMC: 9007978. DOI: 10.1038/s41467-022-29633-6.


References
1.
Mashtalir N, DAvino A, Michel B, Luo J, Pan J, Otto J . Modular Organization and Assembly of SWI/SNF Family Chromatin Remodeling Complexes. Cell. 2018; 175(5):1272-1288.e20. PMC: 6791824. DOI: 10.1016/j.cell.2018.09.032. View

2.
Bernier R, Golzio C, Xiong B, Stessman H, Coe B, Penn O . Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 2014; 158(2):263-276. PMC: 4136921. DOI: 10.1016/j.cell.2014.06.017. View

3.
Rother M, Pellegrino S, Smith R, Gatti M, Meisenberg C, Wiegant W . CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks. Nat Commun. 2020; 11(1):5775. PMC: 7666215. DOI: 10.1038/s41467-020-19502-5. View

4.
Zhen T, Kwon E, Zhao L, Hsu J, Hyde R, Lu Y . deficiency delays leukemogenesis in mice induced by . Blood. 2017; 130(22):2431-2442. PMC: 5709785. DOI: 10.1182/blood-2017-04-780106. View

5.
Parenti I, Lehalle D, Nava C, Torti E, Leitao E, Person R . Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy. Hum Genet. 2021; 140(7):1109-1120. PMC: 8197709. DOI: 10.1007/s00439-021-02283-2. View