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Articles

Publisher Correction: ATM and IRAK1 orchestrate two distinct mechanisms of NF-κB activation in response to DNA damage - Nature Structural & Molecular Biology

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By Sunwoo Oh, Eirene Ednacot
| Nature Verified
Correction to: Nature Structural & Molecular Biology https://doi.org/10.1038/s41594-024-01417-0, published online 3 January 2025. In the version of this article initially published, there was a typographical error in the Fig. 6c y-axis label, now reading “p65/GFP,” where “p65” originally read “p6.” The figure is now amended in the HTML and PDF versions of the article. About this article Bournique, E., Sanchez, A., Oh, S. et al.
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Cooperative role of PACT and ADAR1 in preventing aberrant PKR activation by self-derived double-stranded RNA - Nature Communications

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By Lavanya Manjunath, Pedro A. Ortega, Ambrocio Sanchez, Sunwoo Oh, Junyi Li, Dana Duong, Elodie Bournique, Bert L. Semler, Dheva Setiaputra
| Nature Verified
Abstract Double-stranded RNAs (dsRNAs) produced during viral infections are recognized by the innate immune sensor protein kinase R (PKR), triggering a host translation shutoff that inhibits viral replication and propagation.
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Mesoscale DNA features impact APOBEC3A and APOBEC3B deaminase activity and shape tumor mutational landscapes - Nature Communications

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By Ambrocio Sanchez, Pedro A. Ortega, Ramin Sakhtemani, Lavanya Manjunath, Sunwoo Oh, Elodie Bournique, Kyumin Kim, Cameron Durfee, Nuri Alpay Temiz, Xiaojiang S. Chen, Reuben S. Harris
| Nature Verified
Abstract Antiviral DNA cytosine deaminases APOBEC3A and APOBEC3B are major sources of mutations in cancer by catalyzing cytosine-to-uracil deamination. APOBEC3A preferentially targets single-stranded DNAs, with a noted affinity for DNA regions that adopt stem-loop secondary structures.
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