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Publication Detail

Title: Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells.

Authors: Li, Wentao; Liu, Wenjie; Kakoki, Ayano; Wang, Rujin; Adebali, Ogun; Jiang, Yuchao; Sancar, Aziz

Published In J Biol Chem, (2019 04 12)

Abstract: Embryonic stem cells can self-renew and differentiate, holding great promise for regenerative medicine. They also employ multiple mechanisms to preserve the integrity of their genomes. Nucleotide excision repair, a versatile repair mechanism, removes bulky DNA adducts from the genome. However, the dynamics of the capacity of nucleotide excision repair during stem cell differentiation remain unclear. Here, using immunoslot blot assay, we measured repair rates of UV-induced DNA damage during differentiation of human embryonic carcinoma (NTERA-2) cells into neurons and muscle cells. Our results revealed that the capacity of nucleotide excision repair increases as cell differentiation progresses. We also found that inhibition of the apoptotic signaling pathway has no effect on nucleotide excision repair capacity. Furthermore, RNA-Seq-based transcriptomic analysis indicated that expression levels of four core repair factors, xeroderma pigmentosum (XP) complementation group A (XPA), XPC, XPG, and XPF-ERCC1, are progressively up-regulated during differentiation, but not those of replication protein A (RPA) and transcription factor IIH (TFIIH). Together, our findings reveal that increase of nucleotide excision repair capacity accompanies cell differentiation, supported by the up-regulated transcription of genes encoding DNA repair enzymes during differentiation of two distinct cell lineages.

PubMed ID: 30808711 Exiting the NIEHS site

MeSH Terms: Cell Differentiation*; Cell Line, Tumor; DNA Repair*; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; Embryonal Carcinoma Stem Cells/metabolism*; Embryonal Carcinoma Stem Cells/pathology; Endonucleases/genetics; Endonucleases/metabolism; Humans; Muscle Cells/metabolism*; Muscle Cells/pathology; Neoplasm Proteins/genetics; Neoplasm Proteins/metabolism*; Neurons/metabolism*; Neurons/pathology; Nuclear Proteins/genetics; Nuclear Proteins/metabolism; Replication Protein A/genetics; Replication Protein A/metabolism; Transcription Factor TFIIH/genetics; Transcription Factor TFIIH/metabolism; Transcription Factors/genetics; Transcription Factors/metabolism; Xeroderma Pigmentosum Group A Protein/genetics; Xeroderma Pigmentosum Group A Protein/metabolism

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