2022-2024年Marchigiana, Romagnola和Chianina牛品种中两种隐性遗传疾病的患病率

IF 1.8 3区 农林科学 Q2 VETERINARY SCIENCES
Martina Torricelli, Carla Sebastiani, Anna Fratto, Marcella Ciullo, Fiorella Sbarra, Massimo Biagetti
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引用次数: 0

摘要

牛的一些遗传疾病和性状已经在分子水平上进行了表征,确定了DNA位点上的致病基因变异。位于亚平宁山脉的三个主要意大利本土肉牛品种(Chianina, Marchigiana和Romagnola)也对这一发现感兴趣。意大利肉牛的遗传选择由意大利肉牛饲养者国家协会实施,目的是提高肉产量、生长能力和肌肉发育。就情况而言,必须不断监测牛,特别是那些在家谱书中登记了血统的牛,以查明主要的先天性和遗传性疾病,其中包括“大肚腩综合症”和“先天性鱼鳞病”。大肚腩综合征(PCS)与17号染色体上KDM2B基因的错义变异有关,而先天性鱼鳞病(CI)是由FA2H基因中胞嘧啶的插入引起18号染色体上的帧移位引起的。这项工作的目的是介绍在意大利中部地区Marchigiana和Romagnola品种中PCS患病率以及Chianina品种中CI患病率的最新情况。2022-2024年,PCS的杂合率为6.67%,CI的杂合率为5.67%。这些发现表明,应该对牛进行持续监测,并应使用因果变异的基因分型,至少排除携带者的风险交配,以防止由于这两种先天性疾病造成的进一步动物损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of two recessive genetic disorders in Marchigiana, Romagnola and Chianina cattle breeds in the period 2022-2024.

A certain number of inherited diseases and traits in cattle have been characterized at the molecular level, identifying the causative gene variant in the DNA locus. Also the three main native Italian beef cattle breeds located in the Apennine Mountains (Chianina, Marchigiana and Romagnola) are interested by this discovery. Genetic selection in Italian beef cattle is implemented by the National Association of Italian Beef Cattle Breeders, with the aim of improving meat production, growth ability and muscle development. Contextually, bovines, particularly those with pedigree registered in the genealogical book, have to be constantly monitored for the main congenital and hereditary disorders, among them "Paunch Calf syndrome" and "Congenital Ichthyosis". Paunch Calf Syndrome (PCS) is associated with a missense variant in the KDM2B gene on chromosome 17, while Congenital Ichthyosis (CI) is caused by an insertion of a cytosine in FA2H gene causing a frame-shift on chromosome 18. The aim of this work was to present an update of the prevalence of PCS in Marchigiana and Romagnola breeds and of CI in Chianina breed, in the Central Italy territory. In the period 2022-2024, a frequency of 6.67% heterozygous PCS carriers was registered, while for CI, in 2024, a prevalence of 5.67% heterozygous carriers was observed. These findings show that cattle should be constantly monitored and the genotyping of causal variant should be used, at least for excluding risk matings of carriers to prevent further animal losses due to these two congenital disorders.

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来源期刊
Veterinary Research Communications
Veterinary Research Communications 农林科学-兽医学
CiteScore
2.50
自引率
0.00%
发文量
173
审稿时长
3 months
期刊介绍: Veterinary Research Communications publishes fully refereed research articles and topical reviews on all aspects of the veterinary sciences. Interdisciplinary articles are particularly encouraged, as are well argued reviews, even if they are somewhat controversial. The journal is an appropriate medium in which to publish new methods, newly described diseases and new pathological findings, as these are applied to animals. The material should be of international rather than local interest. As it deliberately seeks a wide coverage, Veterinary Research Communications provides its readers with a means of keeping abreast of current developments in the entire field of veterinary science.
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