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Multiomics Analysis of the NAD-PARP1 Axis Reveals a Role for Site-specific ADP-ribosylation in Splicing in Embryonic Stem Cells

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 2022 Jun 2
PMID 35654456
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Abstract

The differentiation of embryonic stem cells (ESCs) into a lineage-committed state is a dynamic process involving changes in cellular metabolism, epigenetic modifications, post-translational modifications, gene expression, and RNA processing. Here we integrated data from metabolomic, proteomic, and transcriptomic assays to characterize how alterations in NAD metabolism during the differentiation of mouse ESCs lead to alteration of the PARP1-mediated ADP-ribosylated (ADPRylated) proteome and mRNA isoform specialization. Our metabolomic analyses indicate that mESCs use distinct NAD biosynthetic pathways in different cell states: the de novo pathway in the pluripotent state, and the salvage and Preiss-Handler pathways as differentiation progresses. We observed a dramatic induction of PARP1 catalytic activity driven by enhanced nuclear NAD biosynthesis during the early stages of mESC differentiation (e.g., within 12 h of LIF removal). PARP1-modified proteins in mESCs are enriched for biological processes related to stem cell maintenance, transcriptional regulation, and RNA processing. The PARP1 substrates include core spliceosome components, such as U2AF35 and U2AF65, whose splicing functions are modulated by PARP1-mediated site-specific ADP-ribosylation. Finally, we observed that splicing is dysregulated genome-wide in knockout mESCs. Together, these results demonstrate a role for the NAD-PARP1 axis in the maintenance of mESC state, specifically in the splicing program during differentiation.

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References
1.
Xie N, Zhang L, Gao W, Huang C, Huber P, Zhou X . NAD metabolism: pathophysiologic mechanisms and therapeutic potential. Signal Transduct Target Ther. 2020; 5(1):227. PMC: 7539288. DOI: 10.1038/s41392-020-00311-7. View

2.
Hendriks I, Larsen S, Nielsen M . An Advanced Strategy for Comprehensive Profiling of ADP-ribosylation Sites Using Mass Spectrometry-based Proteomics. Mol Cell Proteomics. 2019; 18(5):1010-1026. PMC: 6495254. DOI: 10.1074/mcp.TIR119.001315. View

3.
REED R, Maniatis T . A role for exon sequences and splice-site proximity in splice-site selection. Cell. 1986; 46(5):681-90. DOI: 10.1016/0092-8674(86)90343-0. View

4.
Hicks A, Lorenzetti D, Gilley J, Lu B, Andersson K, Miligan C . Nicotinamide mononucleotide adenylyltransferase 2 (Nmnat2) regulates axon integrity in the mouse embryo. PLoS One. 2012; 7(10):e47869. PMC: 3474723. DOI: 10.1371/journal.pone.0047869. View

5.
Katz Y, Wang E, Airoldi E, Burge C . Analysis and design of RNA sequencing experiments for identifying isoform regulation. Nat Methods. 2010; 7(12):1009-15. PMC: 3037023. DOI: 10.1038/nmeth.1528. View