Suppr超能文献

新斯科舍诱鸭寻回犬视神经乳头缺损的基因分析显示与NHEJ1内含子缺失(柯利犬眼异常突变)不一致。

Genetic analysis of optic nerve head coloboma in the Nova Scotia Duck Tolling Retriever identifies discordance with the NHEJ1 intronic deletion (collie eye anomaly mutation).

作者信息

Brown Emily A, Thomasy Sara M, Murphy Christopher J, Bannasch Danika L

机构信息

Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, 95616, USA.

Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.

出版信息

Vet Ophthalmol. 2018 Mar;21(2):144-150. doi: 10.1111/vop.12488. Epub 2017 Jul 12.

Abstract

Collie eye anomaly (CEA) encompasses a spectrum of different ophthalmic phenotypes from clinically inconsequential choroidal hypoplasia to blindness from coloboma of the optic nerve head (ONH). A previous study found a 7.8-kb deletion in intron 4 of the NHEJ1 gene to be associated with CEA. A genetic test based on this association is recommended for many breeds, including the Nova Scotia Duck Tolling Retriever (NSDTR). Collection of ONH coloboma-affected NSDTR showed lack of concordance of the NHEJ1 intronic deletion with ONH coloboma. Using genomewide single nucleotide polymorphism (SNP) genotyping in 7 ONH coloboma-affected NSDTR cases and 47 unaffected NSDTR controls with no ophthalmic signs, one SNP, located on chromosome 7, demonstrated genomewide significance. However, high genomic inflation may have confounded the results. Therefore, the genomewide association study was repeated using EMMAX to control for population structure in the cohort of 7 cases and 47 controls. However, no regions of the genome were significantly associated with ONH coloboma. These results failed to document significant association with the CEA locus. Due to the complex genetic etiology of ONH coloboma, the NHEJ1 intronic deletion test results should be carefully considered when making breeding decisions. If the goal is to select for visually competent dogs, our data suggest that eye examinations of puppies would be more effective as a guide in selection of breeding pairs than relying solely on currently available genetic tests.

摘要

柯利犬眼异常(CEA)涵盖了一系列不同的眼科表型,从临床上无明显影响的脉络膜发育不全到因视神经乳头(ONH)缺损导致的失明。先前的一项研究发现,NHEJ1基因内含子4中的一个7.8 kb缺失与CEA相关。对于包括新斯科舍诱鸭寻回犬(NSDTR)在内的许多犬种,建议进行基于这种关联的基因检测。收集受ONH缺损影响的NSDTR样本发现,NHEJ1内含子缺失与ONH缺损不一致。在7例受ONH缺损影响的NSDTR病例和47例无眼科症状的未受影响的NSDTR对照中进行全基因组单核苷酸多态性(SNP)基因分型,位于7号染色体上的一个SNP显示出全基因组显著性。然而,高基因组膨胀可能混淆了结果。因此,使用EMMAX对7例病例和47例对照的队列中的群体结构进行控制,重复进行全基因组关联研究。然而,基因组中没有区域与ONH缺损显著相关。这些结果未能证明与CEA位点有显著关联。由于ONH缺损的遗传病因复杂,在做出育种决策时应仔细考虑NHEJ1内含子缺失检测结果。如果目标是选择具有正常视力的犬只,我们的数据表明,对幼犬进行眼部检查作为选择繁殖对的指导比仅依靠目前可用的基因检测更有效。

相似文献

2
Genotypic and allelic frequency of a mutation in the gene associated with collie eye anomaly in dogs in Italy.
Vet Rec Open. 2022 Jan 29;9(1):e26. doi: 10.1002/vro2.26. eCollection 2022 Dec.
4
Collie Eye Anomaly in Switzerland.
Schweiz Arch Tierheilkd. 2009 Dec;151(12):597-603. doi: 10.1024/0036-7281.151.12.597.
5
Compliance between clinical and genetic diagnosis of choroidal hypoplasia in 103 Norwegian Border Collie puppies.
Vet Ophthalmol. 2018 Jul;21(4):371-375. doi: 10.1111/vop.12520. Epub 2017 Nov 7.
6
Collie eye anomaly in Hokkaido dogs: case study.
Vet Ophthalmol. 2012 Mar;15(2):128-32. doi: 10.1111/j.1463-5224.2011.00950.x. Epub 2011 Sep 29.
7
Collie eye anomaly in a mixed-breed dog.
Vet Ophthalmol. 2005 Sep-Oct;8(5):357-60. doi: 10.1111/j.1463-5224.2005.00417.x.
8
Collie Eye Anomaly in Australian Kelpie dogs in Poland.
BMC Vet Res. 2019 Nov 4;15(1):392. doi: 10.1186/s12917-019-2143-y.

引用本文的文献

本文引用的文献

2
Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.
Birth Defects Res C Embryo Today. 2015 Jun;105(2):96-113. doi: 10.1002/bdrc.21097. Epub 2015 Jun 3.
3
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate.
PLoS Genet. 2015 Mar 23;11(3):e1005059. doi: 10.1371/journal.pgen.1005059. eCollection 2015 Mar.
4
A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma.
PLoS One. 2014 Nov 5;9(11):e111941. doi: 10.1371/journal.pone.0111941. eCollection 2014.
5
The genetic architecture of microphthalmia, anophthalmia and coloboma.
Eur J Med Genet. 2014 Aug;57(8):369-80. doi: 10.1016/j.ejmg.2014.05.002. Epub 2014 May 22.
6
A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence.
PLoS Genet. 2014 Apr 3;10(4):e1004257. doi: 10.1371/journal.pgen.1004257. eCollection 2014 Apr.
7
Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.
JAMA Ophthalmol. 2013 Dec;131(12):1517-24. doi: 10.1001/jamaophthalmol.2013.5305.
8
A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy.
PLoS One. 2013 Aug 28;8(8):e72122. doi: 10.1371/journal.pone.0072122. eCollection 2013.
10
Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed.
PLoS One. 2013 May 31;8(5):e64627. doi: 10.1371/journal.pone.0064627. Print 2013.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验