AI Article Synopsis

  • Scanning transmission electron microscopy tomography with ChromEM staining (ChromSTEM) enables 3D visualization of genome organization at a high resolution.
  • The development of a denoising autoencoder (DAE) using convolutional neural networks allows for improved image processing, effectively reducing noise while preserving structural features of chromatin.
  • The DAE reveals new insights into chromatin structure, demonstrating the absence of the 30 nm fiber and highlighting the presence of compact motifs that affect DNA accessibility.

Article Abstract

Scanning transmission electron microscopy tomography with ChromEM staining (ChromSTEM), has allowed for the three-dimensional study of genome organization. By leveraging convolutional neural networks and molecular dynamics simulations, we have developed a denoising autoencoder (DAE) capable of postprocessing experimental ChromSTEM images to provide nucleosome-level resolution. Our DAE is trained on synthetic images generated from simulations of the chromatin fiber using the 1-cylinder per nucleosome (1CPN) model of chromatin. We find that our DAE is capable of removing noise commonly found in high-angle annular dark field (HAADF) STEM experiments and is able to learn structural features driven by the physics of chromatin folding. The DAE outperforms other well-known denoising algorithms without degradation of structural features and permits the resolution of α-tetrahedron tetranucleosome motifs that induce local chromatin compaction and mediate DNA accessibility. Notably, we find no evidence for the 30 nm fiber, which has been suggested to serve as the higher-order structure of the chromatin fiber. This approach provides high-resolution STEM images that allow for the resolution of single nucleosomes and organized domains within chromatin dense regions comprising of folding motifs that modulate the accessibility of DNA to external biological machinery.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311656PMC
http://dx.doi.org/10.1021/acscentsci.3c00178DOI Listing

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