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Open AccessJournal ArticleDOI

Proteome dynamics at broken replication forks reveal a distinct ATM-directed repair response suppressing DNA double-strand break ubiquitination

TLDR
In this article, the authors used nascent chromatin capture (NCC) proteomics to characterize the repair of replication-associated DNA double-strand breaks (DSBs) triggered by topoisomerase 1 (TOP1) inhibitors.
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This article is published in Molecular Cell.The article was published on 2021-03-04 and is currently open access. It has received 37 citations till now. The article focuses on the topics: DNA repair & DNA replication.

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Cracking chromatin with proteomics: From chromatome to histone modifications

TL;DR: This review gives an overview of the proteomic approaches that have been developed by combining mass spectrometry‐based with tailored biochemical and genetic methods to examine overall protein make‐up of chromatin, to characterize chromatin domains, to determine protein interactions, and to decipher the broad spectrum of histone modifications that represent the quintessence of Chromatin function.
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A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis.

TL;DR: In this article, the authors investigated the possible relationship between the propagation of epigenetic information and the developmental cell proliferation during Xenopus embryogenesis and showed that the inhibition of cell proliferation is principally compatible with embryo survival and cellular differentiation.
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Higher‐order modular regulation of the human proteome

TL;DR: ProgulonFinder as mentioned in this paper is a web application that enables the targeted search for progulons of specific cellular processes and reveal multiple new replication factors, validated by extensive phenotyping of siRNA-induced knockdown.
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Genetic requirements for repair of lesions caused by single genomic ribonucleotides in S phase

TL;DR: In this article , a cell cycle phase restricted allele of RNase H2 was used to nick at rNMPs in S phase and study their repair. But, the results were limited to single-ended double-strand breaks (DSBs).
References
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Journal ArticleDOI

Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks

TL;DR: Several case studies of Cytoscape plug-ins are surveyed, including a search for interaction pathways correlating with changes in gene expression, a study of protein complexes involved in cellular recovery to DNA damage, inference of a combined physical/functional interaction network for Halobacterium, and an interface to detailed stochastic/kinetic gene regulatory models.
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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.

TL;DR: By following this protocol, investigators are able to gain an in-depth understanding of the biological themes in lists of genes that are enriched in genome-scale studies.
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Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

TL;DR: The survey will help tool designers/developers and experienced end users understand the underlying algorithms and pertinent details of particular tool categories/tools, enabling them to make the best choices for their particular research interests.
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MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification.

TL;DR: MaxQuant, an integrated suite of algorithms specifically developed for high-resolution, quantitative MS data, detects peaks, isotope clusters and stable amino acid isotope–labeled (SILAC) peptide pairs as three-dimensional objects in m/z, elution time and signal intensity space and achieves mass accuracy in the p.p.b. range.
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