荷兰矮兔(Oryctolagus Cuniculus)高迁移率 AT-hook 2 基因 12.1 kb 缺失的分子检测与关联

IF 3 Q2 CHEMISTRY, ANALYTICAL Analytical science advances Pub Date : 2024-06-02 DOI:10.1002/ansa.202300050
Tai Duc Nguyen, Lam Van Dang, Phuong Nhu Nguyen Tran, Dai Van Nguyen, Anh Phu Nam Bui
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摘要

兔子主要是为人类消费和医学研究而饲养的。不过,最近有研究表明,有几个品种的兔子也作为宠物供人休闲。目前,荷兰矮兔因其个性和迷你身材受到许多越南消费者的极大关注。然而,4 号染色体上的高迁移率 AT 钩 2(HMGA2)基因从 44 709 089 到 44 721 236 bp 位置的 12.1 kb 缺失被确定为导致该品种侏儒症和颅面发育改变的结构变异。有资料表明,HMGA2 在调节生长方面起着重要作用,基因型为 HMGA2 del/del 的个体在出生几天后就会死亡。尽管荷兰矮兔具有很高的经济价值,但越南尚未对该品种的致死等位基因进行遗传调查。本研究的目的是开发一种快速、可靠的方法来筛查越南南部 HMGA2 致命等位基因的频率。采集兔子唾液,然后提取 DNA。优化并使用三种引物进行多重聚合酶链反应(PCR),以检测 HMGA2 序列中是否存在 12.1 kb 的缺失。我们的数据显示,荷兰矮兔群体中的 12.1 kb 缺失是通过我们优化的多重 PCR 检测到的。在100只兔子中,分别有34只和16只兔子是同源野生型(+/+)和同源突变型(del/del),50只兔子是杂合型。HMGA2致死等位基因携带者的频率为66%(66/100只)。结果表明,我们成功地开发了一种快速、准确的多重 PCR 方法来检测基因携带者。对基因型的验证是在测序之后进行的。我们建议在交配计划中对携带者和同源野生型动物进行基因选择时采用我们的多重 PCR 程序,以防止兔子后代的致死率。此外,应提高兔子饲养者的意识,监测荷兰矮兔种群的基因构成。不过,由于样本量的限制,今后的研究应采集更多的样本,以更准确地获得 HMGA2 致死等位基因的遗传频率。
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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Molecular detection and association of 12.1 kb deletion within the high mobility AT-hook 2 gene in the Netherlands dwarf rabbit (Oryctolagus Cuniculus)

Rabbits are mainly bred for human consumption and medical research. However, it has been recently showed that several rabbit breeds are also kept as pets for human leisure. The Netherlands dwarf rabbit is currently in the immense interest of many Vietnamese customers due to its personality and miniature stature. However, 12.1 kb deletion from position 44,709,089 to 44,721,236 bp in the high mobility AT-hook 2 (HMGA2) gene on chromosome 4 was identified as the structural variant causing dwarfism and altered craniofacial development in this breed. It has been documented that HMGA2 plays an important role in regulating growth and individuals with genotype HMGA2 del/del are fatal several days after birth. Despite the economically high value of the Netherlands dwarf rabbit, there has been no study on the genetic survey of lethal alleles in this breed in Vietnam. The aim of this study is to develop a fast and reliable method to screen the frequency of lethal alleles of HMGA2 in the South of Vietnam. Rabbit saliva was collected, and DNA extraction was followed. Multiplex polymerase chain reaction (PCR) with three primers was optimized and performed to detect the presence of 12.1 kb deletion within the HMGA2 sequence. Our data showed that the 12.1 kb deletion in the Netherlands dwarf rabbit population was detected by our optimized multiplex PCR. In 100 rabbit animals, 34 and 16 individuals were homozygous wild type (+/+) and homozygous mutant (del/del), respectively, while 50 rabbits were heterozygous. The frequency of HMGA2 lethal allele carrier was 66% (66/100 individuals). Our results indicated that we successfully developed a fast, accurate multiplex PCR to detect carrier individuals. Verification of the genotypes was followed by sequencing. We recommend implementing our multiplex PCR procedure in genetic selection for carrier and homozygous wild-type animals in the mating scheme to prevent the lethality of the rabbit offspring. Additionally, awareness should be raised among rabbit breeders to monitor the genetic makeup of the Netherlands dwarf rabbit populations. However, due to the limitation of the sample size, more samples should be taken in future studies to obtain the genetic frequency of the HMGA2 lethal allele more accurately.

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