Assessing SMC Complex Function in Replication Fork Progression with DNA Fiber Assays

Abstract

Chromosome organization undergoes substantial changes during S phase, as parental strands unzip at replication forks to create sister chromatids. Structural Maintenance of Chromosomes (SMC) complexes actively organize chromatin fibers in the wake of the replication fork during a normal S phase, but also in response to replicative stress, thereby influencing replication dynamics. The DNA fiber assay is a relatively simple and cheap technique that allows the study of replication dynamics by sequential incorporation of two nucleotide analogs, followed by DNA spreading and immunodetection of replicated tracks. Here, we present a step-by-step protocol to perform DNA fiber assays in human cell lines, providing a quantitative approach to analyze replication fork progression. As an example, we describe its application in wild-type and SMC5/6 mutant cells, treated or not with hydroxyurea to induce replicative stress. This method can be easily customized to other cell types, alternative strategies for SMC complex inactivation, or treatments that perturb DNA replication. In addition, by modifying culture conditions, this approach can be used to investigate not only fork rate but also fork reversal, fork restart, fork protection, and other aspects of global replication dynamics regulated by SMC activities.


Work in JT-R lab is supported by grant PID2021-127689NB-I00 from MICIN/AEI/ 10.13039/501100011033/ and European Union Regional Funds (FEDER). The IRBLLEIDA institute is part of the CERCA. NPL was supported by a “Formación de doctores” fellowship (FPI/ PRE2019-090744) and S by a UdL predoctoral fellowship.

Document Type

Article


Accepted version

Language

English

Subjects and keywords

Chromosome; CldU; DNA fiber; DNA repair; DNA replication

Publisher

Springer Nature

Related items

127689

Versió postprint del document publicat a: https://doi.org/10.1007/978-1-0716-5005-9_10

Methods in molecular biology, 2026, vol. 2991, p. 149-162

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Rights

(c) The Author(s), 2026

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