Global patterns of apparent copy number variation in birds revealed by cross-species comparative genomic hybridization

被引:0
|
作者
Benjamin M. Skinner
Abdullah Al Mutery
Deborah Smith
Martin Völker
Nilofour Hojjat
Sannaa Raja
Steven Trim
Peter Houde
William J. Boecklen
Darren K. Griffin
机构
[1] University of Kent,School of Biosciences
[2] University of Cambridge,Department of Pathology
[3] University of Sharjah,Department of Applied Biology
[4] New Mexico State University,Department of Biology
来源
Chromosome Research | 2014年 / 22卷
关键词
evolution; avian; chromosome; microarray; CNVs; array-CGH;
D O I
暂无
中图分类号
学科分类号
摘要
There is a growing interest in copy number variation (CNV) and the recognition of its importance in phenotype, disease, adaptation and speciation. CNV data is usually ascertained by array-CGH within-species, but similar inter-species comparisons have also been made in primates, mice and domestic mammals. Here, we conducted a broad appraisal of putative cross-species CNVs in birds, 16 species in all, using the standard array-CGH approach. Using a chicken oligonucleotide microarray, we detected 790 apparent CNVs within 135 unique regions and developed a bioinformatic tool ‘CNV Analyser’ for analysing and visualising cross-species data sets. We successfully addressed four hypotheses as follows: (a) Cross-species CNVs (compared to chicken) are, as suggested from preliminary evidence, smaller and fewer in number than in mammals; this ‘dogma’ was rejected in the light of the new evidence. (b) CNVs in birds are likely to have a functional effect through an association with genes; a large proportion of detected regions (70 %) were indeed associated with genes (suggesting functional significance), however, not necessarily more so than in mammals. (c) There are more CNVs in birds with more rearranged karyotypes; this hypothesis was rejected. Indeed, Falco species contained fewer than most with relatively standard (chicken-like) karyotypes. (d) There are more CNVs per megabase on micro-chromosomes than macrochromosomes; this hypothesis was accepted. Indeed, in species with rearranged karyotypes characterised by chromosomal fusions, the fused former microchromosomes still ‘behaved’ as though they were their microchromosomal ancestors. Gene ontology analysis of CNVRs revealed enrichment in immune response and antigen presentation genes and five CNVRs were perfectly correlated with the unique loss of sexual dichromatism in one Galliformes species.
引用
收藏
页码:59 / 70
页数:11
相关论文
共 50 条
  • [31] Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization
    Fan, Yao-Shan
    Jayakar, Parul
    Zhu, Hongbo
    Barbouth, Deborah
    Sacharow, Stephanie
    Morales, Ana
    Carver, Virginia
    Benke, Paul
    Mundy, Peter
    Elsas, Louis J.
    HUMAN MUTATION, 2007, 28 (11) : 1124 - 1132
  • [32] Array-based comparative genomic hybridization for the detection of DNA sequence copy number changes in Barrett's adenocarcinoma
    Albrecht, B
    Hausmann, M
    Zitzelsberger, H
    Stein, H
    Siewert, JR
    Hopt, U
    Langer, R
    Höfler, H
    Werner, M
    Walch, A
    JOURNAL OF PATHOLOGY, 2004, 203 (03) : 780 - 788
  • [33] Investigation of copy number variations on chromosome 21 detected by comparative genomic hybridization (CGH) microarray in patients with congenital anomalies
    Wenfu Li
    Xianfu Wang
    Shibo Li
    Molecular Cytogenetics, 11
  • [34] Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth
    Malan, Valerie
    Chevallier, Suzanne
    Soler, Gwendoline
    Coubes, Christine
    Lacombe, Didier
    Pasquier, Laurent
    Soulier, Jean
    Morichon-Delvallez, Nicole
    Turleau, Catherine
    Munnich, Arnold
    Romana, Serge
    Vekemans, Michel
    Cormier-Daire, Valerie
    Colleaux, Laurence
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2010, 18 (02) : 227 - 232
  • [35] Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth
    Valérie Malan
    Suzanne Chevallier
    Gwendoline Soler
    Christine Coubes
    Didier Lacombe
    Laurent Pasquier
    Jean Soulier
    Nicole Morichon-Delvallez
    Catherine Turleau
    Arnold Munnich
    Serge Romana
    Michel Vekemans
    Valérie Cormier-Daire
    Laurence Colleaux
    European Journal of Human Genetics, 2010, 18 : 227 - 232
  • [36] Similarities and differences in the nuclear genome organization within Pooideae species revealed by comparative genomic in situ hybridization (GISH)
    Majka, Joanna
    Majka, Maciej
    Kwiatek, Micha
    Wisniewska, Halina
    JOURNAL OF APPLIED GENETICS, 2017, 58 (02) : 151 - 161
  • [37] A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease
    Valentina La Cognata
    Giovanna Morello
    Giulia Gentile
    Velia D’Agata
    Chiara Criscuolo
    Francesca Cavalcanti
    Sebastiano Cavallaro
    neurogenetics, 2016, 17 : 233 - 244
  • [38] Meta-analysis and pooled re-analysis of copy number changes in colorectal cancer detected by comparative genomic hybridization
    Hughes, Simon
    Williams, Richard D.
    Webb, Emily
    Houlston, Richard S.
    ANTICANCER RESEARCH, 2006, 26 (5A) : 3439 - 3444
  • [39] Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas
    Ana Belén Espinosa
    Carlos Mackintosh
    Angel Maíllo
    Laura Gutierrez
    Pablo Sousa
    Marta Merino
    Javier Ortiz
    Enrique de Alava
    Alberto Orfao
    María Dolores Tabernero
    European Journal of Human Genetics, 2008, 16 : 1450 - 1458
  • [40] The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
    Wayhelova, Marketa
    Smetana, Jan
    Vallova, Vladimira
    Hladilkova, Eva
    Filkova, Hana
    Hanakova, Marta
    Vilemova, Marcela
    Nikolova, Petra
    Gromesova, Barbora
    Gaillyova, Renata
    Kuglik, Petr
    BMC MEDICAL GENOMICS, 2019, 12 (1)