Agricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, 38000, Pakistan.
Department of Animal Breeding and Genetics, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Mol Biol Rep. 2024 Sep 5;51(1):963. doi: 10.1007/s11033-024-09898-4.
Bovine leukocyte adhesion deficiency (BLAD), bovine citrullinemia (BC), and deficiency of Uridine monophosphate synthetase (DUMPS) are the common autosomal recessive disorders affecting the global dairy industry. BLAD leads to poor wound healing and recurrent infections. In BC, ammonia builds up leading to neurological disorders and death. DUMPS results in developmental abnormalities.
In this study, tetra-primer amplification refractory mutation system polymerase chain reaction (ARMS PCR) based diagnostic tests were optimized for BLAD, BC, and DUMPS. A total of 250 animals (58 indigenous and 192 Holstein Friesian (HF)) were screened from all across Pakistan. In addition to validation of ARMS-PCR results through Sanger sequencing, the protein modeling provided structural insights of the disease-associated reported SNPs. Pathway analysis illustrated gene functions under normal and mutated conditions. Furthermore, haplotype and phylogenetic analysis of ASS1 (Argininosuccinate synthetase) gene were performed on study samples and NCBI retrieved sequences.
The study's focus was to screen the herds for prevalence of carriers of genetic disorders, as they are the main source of disease dissemination. One animal was found carrier for BC, whereas no carriers were found for BLAD and DUMPS. The protein models corroborated the reported amino acid change in BLAD, and protein truncation in both BC and DUMPS proteins. SNPs found in NCBI retrieved sequences were either silent or missense and had no effect on protein structure. DNA network presented graphical illustration of haplotype interactions and phylogenetic analysis conferred evolutionary landscape of ASS1 gene. The combination of these approaches produced an in-depth genetic picture of BC in Pakistani cattle.
The development of diagnostic tests and identification of the heterozygous BC sample underscores the significance of constant monitoring to avoid the unwanted dissemination of mutant alleles among Pakistani cattle, thereby promoting the general well-being and sustainability of the dairy sector.
牛白细胞黏附缺陷症(BLAD)、牛瓜氨酸血症(BC)和尿苷一磷酸合酶缺乏症(DUMPS)是影响全球奶牛养殖业的常见常染色体隐性遗传病。BLAD 导致伤口愈合不良和反复感染。在 BC 中,氨的积累会导致神经紊乱和死亡。DUMPS 导致发育异常。
本研究针对 BLAD、BC 和 DUMPS 优化了基于四引物扩增受阻突变系统聚合酶链反应(ARMS-PCR)的诊断检测。从巴基斯坦各地共筛选了 250 只动物(58 只本地牛和 192 只荷斯坦弗里生牛)。除了通过 Sanger 测序验证 ARMS-PCR 结果外,还对疾病相关报道的 SNP 进行了蛋白质建模,提供了结构见解。通路分析说明了正常和突变条件下基因的功能。此外,对 ASS1(精氨酸琥珀酸合成酶)基因进行了研究样本和 NCBI 检索序列的单倍型和系统发育分析。
本研究的重点是筛选携带遗传疾病的牛群,因为它们是疾病传播的主要来源。发现一只动物为 BC 携带者,而 BLAD 和 DUMPS 携带者均未发现。蛋白质模型证实了 BLAD 中报道的氨基酸变化,以及 BC 和 DUMPS 蛋白中的蛋白截断。在 NCBI 检索序列中发现的 SNP 要么是沉默的,要么是错义的,对蛋白质结构没有影响。DNA 网络呈现了单倍型相互作用的图形说明,系统发育分析提供了 ASS1 基因的进化景观。这些方法的结合为巴基斯坦牛的 BC 提供了深入的遗传图像。
诊断测试的开发和杂合 BC 样本的鉴定强调了持续监测的重要性,以避免突变等位基因在巴基斯坦牛中的不必要传播,从而促进奶牛养殖业的整体福祉和可持续性。