Literature DB >> 34051743

Detection of copy number variants in African goats using whole genome sequence data.

Wilson Nandolo1,2, Gábor Mészáros1, Maria Wurzinger1, Liveness J Banda2, Timothy N Gondwe2, Henry A Mulindwa3, Helen N Nakimbugwe4, Emily L Clark5, M Jennifer Woodward-Greene6,7, Mei Liu6, George E Liu6, Curtis P Van Tassell6, Benjamin D Rosen8, Johann Sölkner1.   

Abstract

BACKGROUND: Copy number variations (CNV) are a significant source of variation in the genome and are therefore essential to the understanding of genetic characterization. The aim of this study was to develop a fine-scaled copy number variation map for African goats. We used sequence data from multiple breeds and from multiple African countries.
RESULTS: A total of 253,553 CNV (244,876 deletions and 8677 duplications) were identified, corresponding to an overall average of 1393 CNV per animal. The mean CNV length was 3.3 kb, with a median of 1.3 kb. There was substantial differentiation between the populations for some CNV, suggestive of the effect of population-specific selective pressures. A total of 6231 global CNV regions (CNVR) were found across all animals, representing 59.2 Mb (2.4%) of the goat genome. About 1.6% of the CNVR were present in all 34 breeds and 28.7% were present in all 5 geographical areas across Africa, where animals had been sampled. The CNVR had genes that were highly enriched in important biological functions, molecular functions, and cellular components including retrograde endocannabinoid signaling, glutamatergic synapse and circadian entrainment.
CONCLUSIONS: This study presents the first fine CNV map of African goat based on WGS data and adds to the growing body of knowledge on the genetic characterization of goats.

Entities:  

Keywords:  African goats; Copy number variations; Whole genome sequence

Year:  2021        PMID: 34051743     DOI: 10.1186/s12864-021-07703-1

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


  69 in total

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Authors:  A John Iafrate; Lars Feuk; Miguel N Rivera; Marc L Listewnik; Patricia K Donahoe; Ying Qi; Stephen W Scherer; Charles Lee
Journal:  Nat Genet       Date:  2004-08-01       Impact factor: 38.330

Review 2.  Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.

Authors:  Jacques S Beckmann; Xavier Estivill; Stylianos E Antonarakis
Journal:  Nat Rev Genet       Date:  2007-08       Impact factor: 53.242

Review 3.  A decade of structural variants: description, history and methods to detect structural variation.

Authors:  Geòrgia Escaramís; Elisa Docampo; Raquel Rabionet
Journal:  Brief Funct Genomics       Date:  2015-04-15       Impact factor: 4.241

Review 4.  Structural variation in the sequencing era.

Authors:  Steve S Ho; Alexander E Urban; Ryan E Mills
Journal:  Nat Rev Genet       Date:  2019-11-15       Impact factor: 53.242

5.  Mobile interspersed repeats are major structural variants in the human genome.

Authors:  Cheng Ran Lisa Huang; Anna M Schneider; Yunqi Lu; Tejasvi Niranjan; Peilin Shen; Matoya A Robinson; Jared P Steranka; David Valle; Curt I Civin; Tao Wang; Sarah J Wheelan; Hongkai Ji; Jef D Boeke; Kathleen H Burns
Journal:  Cell       Date:  2010-06-25       Impact factor: 41.582

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Authors:  Richard Redon; Shumpei Ishikawa; Karen R Fitch; Lars Feuk; George H Perry; T Daniel Andrews; Heike Fiegler; Michael H Shapero; Andrew R Carson; Wenwei Chen; Eun Kyung Cho; Stephanie Dallaire; Jennifer L Freeman; Juan R González; Mònica Gratacòs; Jing Huang; Dimitrios Kalaitzopoulos; Daisuke Komura; Jeffrey R MacDonald; Christian R Marshall; Rui Mei; Lyndal Montgomery; Kunihiro Nishimura; Kohji Okamura; Fan Shen; Martin J Somerville; Joelle Tchinda; Armand Valsesia; Cara Woodwark; Fengtang Yang; Junjun Zhang; Tatiana Zerjal; Jane Zhang; Lluis Armengol; Donald F Conrad; Xavier Estivill; Chris Tyler-Smith; Nigel P Carter; Hiroyuki Aburatani; Charles Lee; Keith W Jones; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2006-11-23       Impact factor: 49.962

Review 7.  Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.

Authors:  Jonathan Sebat; Deborah L Levy; Shane E McCarthy
Journal:  Trends Genet       Date:  2009-10-31       Impact factor: 11.639

8.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

Review 9.  The population genetics of structural variation.

Authors:  Donald F Conrad; Matthew E Hurles
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

10.  Evolution of genomic structural variation and genomic architecture in the adaptive radiations of African cichlid fishes.

Authors:  Shaohua Fan; Axel Meyer
Journal:  Front Genet       Date:  2014-06-03       Impact factor: 4.599

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Journal:  BMC Genomics       Date:  2022-06-21       Impact factor: 4.547

2.  Genome-wide detection of copy number variation in American mink using whole-genome sequencing.

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