» Articles » PMID: 30424520

Global Identification of HIF-1α Target Genes in Benzene Poisoning Mouse Bone Marrow Cells

Overview
Publisher MDPI
Date 2018 Nov 15
PMID 30424520
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Benzene is a hematopoietic toxicant, and hematopoietic cells in bone marrow (BM) are one of the main targets for its action, especially hematopoietic stem cells (HSCs). Hypoxia-inducible factor-1α (HIF-1α) is associated with the metabolism and physiological functions of HSCs. We previously found that the mechanism of regulation of HIF-1α is involved in benzene-induced hematopoietic toxicity. In this study, chromatin immunoprecipitation sequencing (ChIP-Seq) technologies were used to analyze the genome-wide binding spectrum of HIF-1α in mouse BM cells, and specific HIF-1α target genes and pathways associated with benzene toxicity were screened and validated. By application of the ChIP-Seq technique, we identified target genes HIF-1α directly binds to and regulates. Forty-two differentially down-regulated genes containing the HIF-1α specific binding site hypoxia response element (HRE) were found, of which 25 genes were with biological function. Moreover, the enrichment analysis of signal pathways indicated that these genes were significantly enriched in the Jak-STAT signaling pathway, Natural killer cell mediated cytotoxicity, the Fc epsilon RI signaling pathway, Pyrimidine metabolism, the T cell receptor signaling pathway, and Transcriptional misregulation in cancer. After verification, 11 genes involved in HSC self-renewal, cell cycle, differentiation, and apoptosis pathways were found to be significantly reduced, and may participate in benzene-induced hematotoxicity. Our study provides a new academic clue for the mechanism of benzene hematotoxicity.

Citing Articles

Analysis of self-renewing and differentiation-related microRNAs and transcription factors in multilineage mouse hematopoietic stem/progenitor cells induced by 1,4-benzoquinone.

Dewi R, Yusoff N, Razak S, Abd Hamid Z PeerJ. 2023; 11:e15608.

PMID: 37456886 PMC: 10340113. DOI: 10.7717/peerj.15608.


Cellular and Molecular Mechanisms of Environmental Pollutants on Hematopoiesis.

Scharf P, Broering M, da Rocha G, Farsky S Int J Mol Sci. 2020; 21(19).

PMID: 32977499 PMC: 7583016. DOI: 10.3390/ijms21196996.


PTP4A3, A Novel Target Gene of HIF-1alpha, Participates in Benzene-Induced Cell Proliferation Inhibition and Apoptosis through PI3K/AKT Pathway.

Pu Y, Sun F, Sun R, Man Z, Ji S, Xu K Int J Environ Res Public Health. 2020; 17(3).

PMID: 32024182 PMC: 7037067. DOI: 10.3390/ijerph17030910.

References
1.
Cui X, Han Z, He S, Wu X, Chen T, Shao C . HIF1/2α mediates hypoxia-induced LDHA expression in human pancreatic cancer cells. Oncotarget. 2017; 8(15):24840-24852. PMC: 5421893. DOI: 10.18632/oncotarget.15266. View

2.
Sun R, Zhang J, Yin L, Pu Y . Investigation into variation of endogenous metabolites in bone marrow cells and plasma in C3H/He mice exposed to benzene. Int J Mol Sci. 2014; 15(3):4994-5010. PMC: 3975436. DOI: 10.3390/ijms15034994. View

3.
Jang Y, Sharkis S . A low level of reactive oxygen species selects for primitive hematopoietic stem cells that may reside in the low-oxygenic niche. Blood. 2007; 110(8):3056-63. PMC: 2018677. DOI: 10.1182/blood-2007-05-087759. View

4.
Jaakkola P, Mole D, Tian Y, Wilson M, Gielbert J, Gaskell S . Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science. 2001; 292(5516):468-72. DOI: 10.1126/science.1059796. View

5.
Piccoli C, Ria R, Scrima R, Cela O, DAprile A, Boffoli D . Characterization of mitochondrial and extra-mitochondrial oxygen consuming reactions in human hematopoietic stem cells. Novel evidence of the occurrence of NAD(P)H oxidase activity. J Biol Chem. 2005; 280(28):26467-76. DOI: 10.1074/jbc.M500047200. View