Literature DB >> 33737533

Evaluation of genetic diversity and management of disease in Border Collie dogs.

Pamela Xing Yi Soh1, Wei Tse Hsu1, Mehar Singh Khatkar2, Peter Williamson3.   

Abstract

Maintaining genetic diversity in dog breeds is an important consideration for the management of inherited diseases. We evaluated genetic diversity in Border Collies using molecular and genealogical methods, and examined changes to genetic diversity when carriers for Trapped Neutrophil Syndrome (TNS) and Neuronal Ceroid Lipofuscinosis (NCL) are removed from the genotyped population. Genotype data for 255 Border Collies and a pedigree database of 83,996 Border Collies were used for analysis. Molecular estimates revealed a mean multi-locus heterozygosity (MLH) of 0.311 (SD 0.027), 20.79% of the genome consisted of runs of homozygosity (ROH ) > 1 Mb, effective population size (Ne) was 84.7, and mean inbreeding (F) was 0.052 (SD 0.083). For 227 genotyped Border Collies that had available pedigree information (GenoPed), molecular and pedigree estimates of diversity were compared. A reference population (dogs born between 2005 and 2015, inclusive; N = 13,523; RefPop) and their ancestors (N = 12,478) were used to evaluate the diversity of the population that are contributing to the current generation. The reference population had a Ne of 123.5, a mean F of 0.095 (SD 0.082), 2276 founders (f), 205.5 effective founders (fe), 28 effective ancestors (fa) and 10.65 (SD 2.82) founder genomes (Ng). Removing TNS and NCL carriers from the genotyped population had a small impact on diversity measures (ROH > 1 Mb, MLH, heterozygosity), however, there was a loss of > 10% minor allele frequency for 89 SNPs around the TNS mutation (maximum loss of 12.7%), and a loss of > 5% for 5 SNPs around the NCL mutation (maximum 5.18%). A common ancestor was identified for 38 TNS-affected dogs and 64 TNS carriers, and a different common ancestor was identified for 33 NCL-affected dogs and 28 carriers, with some overlap of prominent individuals between both pedigrees. Overall, Border Collies have a high level of genetic diversity compared to other breeds.

Entities:  

Year:  2021        PMID: 33737533     DOI: 10.1038/s41598-021-85262-x

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  48 in total

1.  Molecular prevalence of multiple genetic disorders in Border collies in Japan and recommendations for genetic counselling.

Authors:  K Mizukami; A Yabuki; M Kohyama; K Kushida; M M Rahman; M M Uddin; M Sawa; O Yamato
Journal:  Vet J       Date:  2016-05-06       Impact factor: 2.688

2.  Neuronal ceroid lipofuscinosis in Salukis is caused by a single base pair insertion in CLN8.

Authors:  F Lingaas; O-A Guttersrud; E Arnet; A Espenes
Journal:  Anim Genet       Date:  2018-02       Impact factor: 3.169

3.  A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs.

Authors:  Scott A Melville; Carmen L Wilson; Chiu S Chiang; Virginia P Studdert; Frode Lingaas; Alan N Wilton
Journal:  Genomics       Date:  2005-09       Impact factor: 5.736

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Journal:  N Z Vet J       Date:  1996-04       Impact factor: 1.628

Review 5.  Canine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions.

Authors:  Martin L Katz; Eline Rustad; Grace O Robinson; Rebecca E H Whiting; Jeffrey T Student; Joan R Coates; Kristina Narfstrom
Journal:  Neurobiol Dis       Date:  2017-08-30       Impact factor: 5.996

6.  Ceroid-lipofuscinosis in border collie dogs.

Authors:  R M Taylor; B R Farrow
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

7.  Inherited defects in pedigree dogs. Part 1: disorders related to breed standards.

Authors:  Lucy Asher; Gillian Diesel; Jennifer F Summers; Paul D McGreevy; Lisa M Collins
Journal:  Vet J       Date:  2009-12       Impact factor: 2.688

8.  Ceroid lipofuscinosis in the border collie dog: retinal lesions in an animal model of juvenile Batten disease.

Authors:  R M Taylor; B R Farrow
Journal:  Am J Med Genet       Date:  1992-02-15

9.  A canine model of Cohen syndrome: Trapped Neutrophil Syndrome.

Authors:  Jeremy R Shearman; Alan N Wilton
Journal:  BMC Genomics       Date:  2011-05-23       Impact factor: 3.969

10.  Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies.

Authors:  A Kolicheski; G S Johnson; D P O'Brien; T Mhlanga-Mutangadura; D Gilliam; J Guo; T D Anderson-Sieg; R D Schnabel; J F Taylor; A Lebowitz; B Swanson; D Hicks; Z E Niman; F A Wininger; M C Carpentier; M L Katz
Journal:  J Vet Intern Med       Date:  2016-05-20       Impact factor: 3.333

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  1 in total

1.  Genome-wide run of homozygosity analysis reveals candidate genomic regions associated with environmental adaptations of Tibetan native chickens.

Authors:  Jingwei Yuan; Shijun Li; Zheya Sheng; Meikun Zhang; Xuming Liu; Zhengdong Yuan; Ning Yang; Jilan Chen
Journal:  BMC Genomics       Date:  2022-01-31       Impact factor: 3.969

  1 in total

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