Schwenger B, Schöber S, Simon D
Institut für Tierzucht und Vererbungsforschung, Tierärztliche Hochschule Hannover, Germany.
Genomics. 1993 Apr;16(1):241-4. doi: 10.1006/geno.1993.1165.
Deficiency of uridine monophosphate synthase (DUMPS) is a monogenic autosomal recessive disorder in cattle, resulting in early embryonic death of homozygous offspring. To identify the mutation responsible for DUMPS, liver RNA from identified, DUMPS heterozygous animals from the Holstein and Red Holstein breeds was reverse transcribed. Amplification of cDNA with sequence-specific primers and subsequent sequencing of the PCR products revealed a mutation (C-->T) with the loss of an AvaI site at codon 405, resulting in a premature stop codon with a truncated C-terminal catalytic subunit of the protein. A direct DNA test based on PCR was developed and subsequently tested on 102 animals. Complete concurrence of deficiency of UMPS and the presence of the described point mutation in heterozygous animals was observed, thus confirming this point mutation as the basic defect in DUMPS cattle.
尿苷单磷酸合酶缺乏症(DUMPS)是牛的一种单基因常染色体隐性疾病,导致纯合子后代早期胚胎死亡。为了鉴定导致DUMPS的突变,对来自荷斯坦和红荷斯坦品种的已鉴定的DUMPS杂合动物的肝脏RNA进行了逆转录。用序列特异性引物扩增cDNA并随后对PCR产物进行测序,结果显示在密码子405处发生了一个突变(C→T),导致AvaI位点缺失,产生了一个截短的蛋白质C末端催化亚基的过早终止密码子。开发了一种基于PCR的直接DNA检测方法,并随后在102只动物上进行了测试。观察到杂合动物中UMPS缺乏与所述点突变的存在完全一致,从而证实该点突变是DUMPS牛的基本缺陷。