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Mechanism of cytarabine-induced neurotoxicity [CRISPR Screen]

ABSTRACT: Mechanism of cytarabine-induced neurotoxicity [CRISPR Screen]

PROVIDER: PRJNA1243422 | ENA |

REPOSITORIES: ENA

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Dataset's files

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			Action	DRS
	SRR32901560_1.fastq.gz	Fastqsanger.gz
	SRR32901560_2.fastq.gz	Fastqsanger.gz
	SRR32901561_1.fastq.gz	Fastqsanger.gz
	SRR32901561_2.fastq.gz	Fastqsanger.gz
	SRR32901562_1.fastq.gz	Fastqsanger.gz

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Mechanism of cytarabine-induced neurotoxicity [CRISPR Screen]

Project description:Postmitotic neurons are known to harbor high levels of methylated cytosine and its oxidized intermediates such as 5hmC, but the functional relevance of these epigenetic modifications of DNA are poorly understood. We show that some but not all cytidine analogs, such as cytarabine, cause DNA double strand breaks (DSB) during TET-mediated active 5mC demethylation by interrupting TDG-dependent base excision repair. These DSBs are frequently converted into indels and translocations by DNA ligase 4. In vivo, Purkinje and Golgi cells in the cerebellum are the only neuronal populations that exhibit high levels of DNA damage to cytarabine. In Purkinje cells, TET targets gene bodies with the highest expression marked by enhancer-associated histone modifications. Many of these genes control movement coordination which explains the long recognized cerebellar neurotoxicity of cytarabine. We show that other cytidine analogs, such as gemcitabine cause only single strand breaks in neurons, which are repaired by DNA ligase 3 with minimal toxicity. Our findings uncover a mechanistic link between TET-mediated DNA demethylation, base excision repair and gene expression in neurons and provide a rational explanation for the different neurotoxicity profiles of an important class of antineoplastic agents.

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Project description:Mechanism of cytarabine-induced neurotoxicity [END-Seq]