Evidence map›Paper›PMID 30355328›Full record

ArticleGenome biology2018

Chromosome-level assembly reveals extensive rearrangement in saker falcon and budgerigar, but not ostrich, genomes.

Rebecca E O'Connor, Marta Farré, Sunitha Joseph, Joana Damas, Lucas Kiazim, Rebecca Jennings, Sophie Bennett, Eden A Slack, Emily Allanson, Denis M Larkin and 1 more

Abstract read
In one paragraph

Article in Genome biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

  1. The complete genome of a songbird.bioRxiv : the preprint server for biology · 2025
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  19. Fourth Report on Chicken Genes and Chromosomes 2022.Cytogenetic and genome research · 2022
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Rebecca E O'ConnorSchool of Biosciences, University of Kent, Canterbury, UK.
Marta FarréDepartment of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, UK.
Sunitha JosephSchool of Biosciences, University of Kent, Canterbury, UK.
Joana DamasDepartment of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, UK.
Lucas KiazimSchool of Biosciences, University of Kent, Canterbury, UK.
Rebecca JenningsSchool of Biosciences, University of Kent, Canterbury, UK.
Sophie BennettSchool of Biosciences, University of Kent, Canterbury, UK.
Eden A SlackDepartment of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, UK.
Emily AllansonDepartment of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, UK.
Denis M LarkinDepartment of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, UK.
Darren K GriffinSchool of Biosciences, University of Kent, Canterbury, UK. d.k.griffin@kent.ac.uk.ORCID 0000-0001-7595-3226

Funding

Biotechnology and Biological Sciences Research Council BB/E010652/1Biotechnology and Biological Sciences Research Council BB/J010170/1Biotechnology and Biological Sciences Research Council BB/K008161/1Biotechnology and Biological Sciences Research Council BB/K008226/1
6 · The paper itself

Abstract

backgroundThe number of de novo genome sequence assemblies is increasing exponentially; however, relatively few contain one scaffold/contig per chromosome. Such assemblies are essential for studies of genotype-to-phenotype association, gross genomic evolution, and speciation. Inter-species differences can arise from chromosomal changes fixed during evolution, and we previously hypothesized that a higher fraction of elements under negative selection contributed to avian-specific phenotypes and avian genome organization stability. The objective of this study is to generate chromosome-level assemblies of three avian species (saker falcon, budgerigar, and ostrich) previously reported as karyotypically rearranged compared to most birds. We also test the hypothesis that the density of conserved non-coding elements is associated with the positions of evolutionary breakpoint regions.

resultsWe used reference-assisted chromosome assembly, PCR, and lab-based molecular approaches, to generate chromosome-level assemblies of the three species. We mapped inter- and intrachromosomal changes from the avian ancestor, finding no interchromosomal rearrangements in the ostrich genome, despite it being previously described as chromosomally rearranged. We found that the average density of conserved non-coding elements in evolutionary breakpoint regions is significantly reduced. Fission evolutionary breakpoint regions have the lowest conserved non-coding element density, and intrachromomosomal evolutionary breakpoint regions have the highest.

conclusionsThe tools used here can generate inexpensive, efficient chromosome-level assemblies, with > 80% assigned to chromosomes, which is comparable to genomes assembled using high-density physical or genetic mapping. Moreover, conserved non-coding elements are important factors in defining where rearrangements, especially interchromosomal, are fixed during evolution without deleterious effects.

Indexed as

GenomeAnimalsChromosomesChromosomes, Artificial, BacterialConserved SequenceDNA, IntergenicFalconiformesGene RearrangementGenomicsMelopsittacusSpecies SpecificityStruthioniformesDNA, IntergenicChromosome-level genome assemblyCNEEBRGenome evolution

Identifiers

PMID30355328
PMCPMC6201548

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.