Saito M, Nakamura T
Department of Crop Breeding, Tohoku National Agriculture Research Center, 4 Akahira, Shimo-Kuriyagawa, Morioka, 020-0198, Iwate, Japan.
Theor Appl Genet. 2005 Jan;110(2):276-82. doi: 10.1007/s00122-004-1830-6. Epub 2004 Dec 8.
In this report, the Wx-A1 mutations carried by a Triticum dicoccoides line from Israel and a Triticum dicoccum line from Yugoslavia are characterized. A single nucleotide insertion in the T. dicoccoides null allele and a single nucleotide deletion in the T. dicoccum null allele each cause frameshift mutations that induce premature termination codons more than 55 nucleotides upstream of the last exon-exon junction. In both mutants, Wx-A1 transcripts were detectable in 10 day post-anthesis endosperm by relative RT-PCR. However, transcript levels of the T. dicoccoides and T. dicoccum null alleles were reduced to approximately 6.5 and 1.5% of wild-type, respectively. Therefore, the lack of Wx-A1 protein in the mutants appears to be largely due to nonsense-mediated mRNA decay. The two mutations described here arose independently, and are not related to either of the Wx-A1 mutations identified in common wheat.
在本报告中,对来自以色列的一粒野生二粒小麦品系和来自南斯拉夫的栽培二粒小麦品系所携带的Wx - A1突变进行了表征。野生二粒小麦无效等位基因中的单个核苷酸插入和栽培二粒小麦无效等位基因中的单个核苷酸缺失均导致移码突变,这些突变在最后一个外显子 - 外显子连接处上游超过55个核苷酸处诱导过早终止密码子。在这两个突变体中,通过相对逆转录聚合酶链反应(RT - PCR)在花后10天的胚乳中可检测到Wx - A1转录本。然而,野生二粒小麦和栽培二粒小麦无效等位基因的转录本水平分别降至野生型的约6.5%和1.5%。因此,突变体中缺乏Wx - A1蛋白似乎主要是由于无义介导的mRNA降解。这里描述的两个突变是独立产生的,与在普通小麦中鉴定出的任何一个Wx - A1突变均无关。