MOLECULAR SCREENING OF COMPLEX VERTEBRAL MALFORMATION AND CITRULLINEMIA CARRIERS IN PAKISTANI NILI-RAVI BUFFALO (BUBALUS BUBALIS) BREEDING BULLS

Pub Date : 2020-01-01 DOI:10.36899/japs.2020.3.0073
K. Zahra, M. Imran, M. Zahoor, K. Ashraf, K. Jaffry, A. Nadeem, I. Rashid, M. Younas, M. Akhtar, W. Shehzad
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引用次数: 1

Abstract

Inherited disorders have serious implications for cattle production and breeding programs. Structural or physiological abnormalities and neonate lethality have negative impacts on breeding populations. Complex vertebral malformation (CVM) and bovine citrullinemia (BC) are heritable congenital syndromes having autosomal recessive basis among cattle breeds worldwide. CVM affected malformed foetuses either get aborted or have evident skeletal deformities upon birth and die during early postnatal period. CVM is caused by a missense substitution (G→T) in uridine diphosphate Nacetylglucosamine transporter encoded by SLC35A3 gene (at position 559). Citrullinemia is a heritable metabolic disorder of urea cycle enzyme argininosuccinate synthetase deficiency which occurs due to a transition (C→T) within exon 5 (codon 86) of ASS1 gene with neurological complications during first week after birth. Both of these fatal disorders have been reported from all over the world in Bos taurus but there is a lack of literature on buffaloes. The present study was carried out to detect CVM and BC carriers among the Pakistani indigenous trans-husbandry water buffalo breed, Nili-Ravi (Bubalus bubalis). In this study, the genetic screening for the target point mutations was carried out using healthy elite buffalo bulls (n=152). Genomic DNA was extracted from the blood and SLC35A3 gene target sequence (281 bp) and ASS1gene target sequence (505 bp) were amplified using PCR. Amplified PCR products were visualized by agarose gel electrophoresis and Sanger sequencing was performed. No carriers were detected among the study sample, however, a novel transversion (c.250C>A) was detected in amplified ASS1 gene fragment. Although, findings of this study confirmed absence of CVM and citrullinemia carriers among the Nili-Ravi buffalo bulls but the presence of carrier animals cannot be ruled out in studies involving larger sample sizes. This genetic screening was carried out for the first time in Pakistani buffaloes which can be used in genetic screening of CVM or BC carrier animals in the future. Further research is recommended in order to enhance the existing data regarding CVM and BC carriers among Bubalus bubalis.
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巴基斯坦尼利拉维水牛(bubalus bubalis)种公牛复杂椎体畸形和瓜氨酸血症携带者的分子筛选
遗传性疾病对牛的生产和育种计划有严重的影响。结构或生理异常和新生儿死亡率对繁殖群体有负面影响。复杂椎体畸形(CVM)和牛瓜氨酸血症(BC)是世界各地牛品种中具有常染色体隐性遗传基础的遗传性先天性综合征。受CVM影响的畸形胎儿要么流产,要么在出生时就有明显的骨骼畸形,并在产后早期死亡。CVM是由SLC35A3基因(559位)编码的尿苷二磷酸Nacetylglucosamine转运体错义置换(G→T)引起的。瓜氨酸血症是一种遗传性代谢紊乱的尿素循环酶精氨酸琥珀酸合成酶缺乏症,发生于ASS1基因外显子5(密码子86)内的转换(C→T),并在出生后第一周出现神经系统并发症。这两种致命疾病在世界各地都有报道,但缺乏关于水牛的文献。本研究在巴基斯坦本土跨牧水牛品种Nili-Ravi (Bubalus bubalis)中检测CVM和BC携带者。在本研究中,使用健康的精英水牛(n=152)进行目标点突变的遗传筛选。从血中提取基因组DNA,用PCR扩增SLC35A3基因靶序列(281 bp)和ass1基因靶序列(505 bp)。扩增的PCR产物通过琼脂糖凝胶电泳显示,并进行Sanger测序。研究样本中未检测到携带者,但在扩增的ASS1基因片段中检测到新的翻转(c.250C> a)。虽然本研究结果证实Nili-Ravi水牛中没有CVM和瓜氨酸血症携带者,但在涉及更大样本量的研究中不能排除携带者动物的存在。这是首次在巴基斯坦水牛中进行遗传筛选,可用于今后CVM或BC携带动物的遗传筛选。建议进一步的研究,以加强现有的资料,CVM和BC的携带者在中国的Bubalus bubalis。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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