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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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Microbial genome evolution is a highly dynamic process shaped by continual gene gain and loss across species and strains. This genomic flexibility allows microorganisms to adapt rapidly to environmental pressures and interactions with other organisms. Central to understanding this diversity is the distinction between the core and pan genomes.The core genome comprises the genes shared by all sampled strains of a species, representing essential functions needed for fundamental cellular processes.
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3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells
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Multiscale evolution of the 3D genome.

Yizhuo Che1, Stephen J Bush2, Kai Ye3

  • 1School of Automation Science and Engineering, Faculty of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi, China; MOE Key Lab for Intelligent Networks & Networks Security, Faculty of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

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|April 25, 2026
PubMed
Summary
This summary is machine-generated.

Genome architecture evolves rapidly at the cellular level and diversifies across species. Convergent evolution shapes higher-order features, linking genome structure to organismal form and function.

Keywords:
3D genomeevolutionmacrolevelmicrolevel

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Area of Science:

  • Genomics
  • Evolutionary Biology
  • Cell Biology

Background:

  • The spatial organization of the genome is crucial for gene regulation and function.
  • Understanding the evolutionary dynamics of genome architecture across different scales remains a challenge.

Purpose of the Study:

  • To synthesize current research on 3D genome evolution from micro- and macro-evolutionary perspectives.
  • To propose a framework for understanding the relationship between genome architecture diversity and the evolution of form and function.

Main Methods:

  • Review of existing literature on 3D genome organization and evolution.
  • Comparative analysis of genome architecture across different timescales (cellular, interspecies, phylogenetic).

Main Results:

  • Genome architecture evolves rapidly at the cellular level (e.g., in cancer) due to mutations and epigenetic changes.
  • Architectural divergence between species is primarily driven by alterations in cis-regulatory elements.
  • Despite diversity, recurrent higher-order genome features have emerged through convergent evolution, reflecting common functional needs.

Conclusions:

  • A micro-to-macro framework can explain the diversity of genome architectures.
  • Genome architecture evolution is intrinsically linked to the evolution of organismal form and function.