4.7 Article

A new emu genome illuminates the evolution of genome configuration and nuclear architecture of avian chromosomes

期刊

GENOME RESEARCH
卷 31, 期 3, 页码 497-511

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gr.271569.120

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资金

  1. National Natural Science Foundation of China [31722050, 31671319, 32061130208]
  2. Natural Science Foundation of Zhejiang Province [LD19C190001]
  3. European Research Council Starting Grant [677696]
  4. European Research Council (ERC) [677696] Funding Source: European Research Council (ERC)

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Emus and other ratites have slower genome evolution rates compared to other birds, making them useful for reconstructing ancestral avian or vertebrate karyotype evolution. The study's findings show that ratites have fewer intra and inter-chromosomal changes than other birds since diverging from turtles. The distinct structure of the emu W chromosome, with highly heterochromatic and recently evolved regions, suggests important early steps in sex chromosome evolution.
Emu and other ratites are more informative than any other birds in reconstructing the evolution of the ancestral avian or vertebrate karyotype because of their much slower rate of genome evolution. Here, we generated a new chromosome-level genome assembly of a female emu, and estimated the tempo of chromosome evolution across major avian phylogenetic branches, by comparing it to chromosome-level genome assemblies of 11 other bird and one turtle species. We found ratites exhibited the lowest numbers of intraand inter-chromosomal changes among birds since their divergence with turtles. The small-sized and gene-rich emu microchromosomes have frequent inter-chromosomal contacts that are associated with housekeeping genes, which appears to be driven by clustering their centromeres in the nuclear interior, away from the macrochromosomes in the nuclear periphery. Unlike nonratite birds, only less than one-third of the emu W Chromosome regions have lost homologous recombination and diverged between the sexes. The emu W is demarcated into a highly heterochromatic region (WS0) and another recently evolved region (WS1) with only moderate sequence divergence with the Z Chromosome. WS1 has expanded its inactive chromatin compartment, increased chromatin contacts within the region, and decreased contacts with the nearby regions, possibly influenced by the spreading of heterochromatin from WS0. These patterns suggest that alteration of chromatin conformation comprises an important early step of sex chromosome evolution. Overall, our results provide novel insights into the evolution of avian genome structure and sex chromosomes in three-dimensional space.

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