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Dinucleotide densities and their distribution patterns vary significantly among species. Previous studies revealed that CpG is susceptible to methylation, enriched at topologically associating domain boundaries and its distribution along the genome correlates with chromatin compartmentalization. However, the multi-scale organizations of CpG in the linear genome, their role in chromatin organization, and how they change along the evolution are only partially understood. By comparing the CpG distribution at different genomic length scales, we quantify the difference between the CpG distributions of different species and evaluate how the hierarchical uneven CpG distribution appears in evolution. The clustering of species based on the CpG distribution is consistent with the phylogenetic tree. Interestingly, we found the CpG distribution and chromatin structure to be correlated in many different length scales, especially for mammals and avians, consistent with the mosaic CpG distribution in the genomes of these species.
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http://dx.doi.org/10.26508/lsa.202101028 | DOI Listing |
Comput Biol Med
August 2025
Departamento de Física, Universidad Autónoma Metropolitana Unidad Iztapalapa, Av. San Rafael Atlixco 186, Leyes de Reforma 1ra Secc, Iztapalapa, 09340, CDMX, Mexico.
Purpose: In this work, we applied the Chaos Game Representation (CGR) to the complete human genomic sequence T2T-CHM13v2.0, analyzing the entire chromosome assembly and individual chromosomes, including mitochondrial DNA, to characterize the fractal structure and multifractal spectra of the genome.
Methods: Multifractal spectra were determined using box-counting coverage.
Zhonghua Yu Fang Yi Xue Za Zhi
August 2025
School of Medicine, University of Electronic Science and Technology of China, Chengdu 610031, China Department of Stomatology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu 610072, China.
To investigate the feasibility of DNA tetrahedral framework (DNA-TH) as a carrier and adjuvant for mucosal vaccines, using streptavidin (SA) as a model antigen. DNA-TH was designed using software, integrating the adjuvant CpG sequence into its structure. After in vitro synthesis, it was conjugated with SA to form SA-DNA-TH nanoparticles.
View Article and Find Full Text PDFBMC Prim Care
August 2025
Department of Pharmacy Practice, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
Background: Obesity has become a public health concern as its prevalence has increased rapidly around the world, including Malaysia. Primary care physicians (PCPs) are the first point of contact for obese patients, playing a crucial role in managing obesity. This study aims to determine the level of obesity care knowledge and practices among PCPs and to identify factors associated with them.
View Article and Find Full Text PDFBiol Reprod
August 2025
Cluster Innovation Centre, University of Delhi, Delhi, India, 110007.
During spermatogenesis, majority of the histones are replaced by protamines to enable the compaction of the sperm chromatin for efficient delivery into the oocyte. Even after the gross histone replacement, some histones are retained in the sperm ranging from 1-15% across mammalian species. The post-translational modifications (PTMs), present on the retained histones of the sperm regulate the embryonic development, post fertilization, making them the suitable candidate for paternal epigenetic inheritance.
View Article and Find Full Text PDFCommun Biol
August 2025
Omics and Computational Biology Program, Izmir Biomedicine and Genome Center, Izmir, Türkiye.
DNMT3A and DNMT3B are closely related DNA methyltransferases that catalyze de novo CpG methylation and have distinct preferences for flanking sequences. Despite sharing 91% sequence similarity within their catalytic domains, these paralogs show non-overlapping genomic targeting and divergent biological roles. To uncover the mechanistic basis of this specificity, we performed 16µs of all-atom molecular dynamics simulations on DNMT3A and DNMT3B complexes bound to CpG substrates with varied +2 flanking bases (i.
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