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RSPO2基因与吉娃娃犬的双侧先天性无肢畸形有关。

The RSPO2 gene is associated with bilateral anterior amelia in Chihuahuas.

作者信息

Chevallier Lucie, Green Marin, Vo Julia, Vernau Karen, Marcellin-Little Denis J, Jagannathan Vidhya, Leeb Tosso, Bannasch Danika

机构信息

INSERM, UPEC, Ecole Nationale Vétérinaire d'Alfort, U955 - IMRB, Team 10 - Biology of the Neuromuscular System, Maisons-Alfort, France.

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

出版信息

Mamm Genome. 2025 Mar 25. doi: 10.1007/s00335-025-10123-1.

Abstract

Bilateral anterior amelia (BAA) is the congenital absence of thoracic limbs and has been reported in the Chihuahua as an autosomal recessive disorder. In some cases, the digits of the pelvic limbs can be variably affected, but otherwise, the pelvic limbs are generally spared. A GWAS performed with nine BAA affected Chihuahuas identified a significant association on chromosome 13, and homozygosity mapping delineated a 2.1 Mb chromosomal region containing the RSPO2 gene. Loss of function variants of RSPO2 in humans and cattle has been associated with the absence of all limbs. Six affected Chihuahuas were whole genome sequenced (WGS) and aligned to the CanFam4 assembly. SNVs, small indels, and structural variants within the critical interval that fitted a recessive model were investigated. Three SNVs (NC_049234.1:g.8891861C > T; NC_049234.1:g.8974204C > T and NC_049234.1:g.9789424G > A) were homozygous in five cases and absent from 3,418 genetically diverse control genome sequences, except for one Small Poodle that was heterozygous. One SNV resided in RSPO2's second intron, while the two others were intergenic. The three candidate variants were genotyped in 7 additional cases and 100 control Chihuahuas. Twelve of 13 cases were homozygous for the mutant allele, and one case was heterozygous. Controls were either homozygous for the reference allele (97%) or heterozygous (3%). Our data should facilitate genetic testing of Chihuahuas to prevent the unintentional production of BAA affected dogs. Moreover, the identification of these variants enhances understanding of RSPO2 gene function in limb development.

摘要

双侧前肢缺如(BAA)是一种先天性胸肢缺失症,在吉娃娃犬中已有报道,为常染色体隐性疾病。在某些情况下,后肢的趾头可能会受到不同程度的影响,但除此之外,后肢通常不受影响。对9只患有BAA的吉娃娃犬进行的全基因组关联研究(GWAS)确定了13号染色体上的一个显著关联,纯合性定位划定了一个包含RSPO2基因的2.1兆碱基染色体区域。人类和牛中RSPO2功能缺失变异与四肢全部缺失有关。对6只患病吉娃娃犬进行了全基因组测序(WGS),并与CanFam4组装序列进行比对。研究了符合隐性模型的关键区间内的单核苷酸变异(SNV)、小插入缺失和结构变异。三个SNV(NC_049234.1:g.8891861C>T;NC_049234.1:g.8974204C>T和NC_049234.1:g.9789424G>A)在5个病例中为纯合子,在3418个基因多样化的对照基因组序列中不存在,但有一只小型贵宾犬为杂合子。一个SNV位于RSPO2的第二个内含子中,另外两个为基因间变异。在另外7个病例和100只对照吉娃娃犬中对这三个候选变异进行了基因分型。13个病例中有12个为突变等位基因纯合子,1个病例为杂合子。对照犬要么为参考等位基因纯合子(97%),要么为杂合子(3%)。我们的数据应有助于对吉娃娃犬进行基因检测,以防止意外繁育出患有BAA的犬只。此外,这些变异的鉴定增进了对RSPO2基因在肢体发育中功能的理解。

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