Shimbata T, Nakamura T, Vrinten P, Saito M, Yonemaru J, Seto Y, Yasuda H
Central Laboratory, Nippon Flour Mills Co. Ltd., 5-1-3 Midorigaoka, Atsugi, Kanagawa, Japan.
Theor Appl Genet. 2005 Oct;111(6):1072-9. doi: 10.1007/s00122-005-0032-1. Epub 2005 Oct 11.
Wheat (Triticum aestivum L.) starch synthase II, which is also known as starch granule protein 1 (SGP-1), plays a major role in endosperm starch synthesis. The three SGP-1 proteins, SGP-A1, B1 and D1, are produced by three homoeologous SSII genes, wSSII-A, B, and D. Lines carrying null alleles for each SGP-1 protein have previously been identified. In this report, the mutations occurring in each wSSII gene were characterized, and PCR-based DNA markers capable of detecting the mutations were developed. In the null wSSII-A allele, a 289 bp deletion accompanied by 8 bp of filler DNA was present near the initiation codon. A 175 bp insertion occurred in exon 8 of the null wSSII-B allele. The insertion represented a recently discovered miniature inverted-repeat transposable element (MITE) named Hikkoshi that was first found in a wheat waxy gene. A 63 bp deletion was found at the region surrounding the junction of the fifth exon and intron of the null wSSII-D allele. Based on this information, we designed primer sets to enable us to conduct allele-specific amplifications for each locus. The applicability of these primer sets for breeding programs was demonstrated by reconstructing a line lacking all three SGP-1 proteins using marker-assisted selection. These markers will also be useful in breeding programs aimed at obtaining partial mutants missing one or two SGP-1 proteins.
小麦(Triticum aestivum L.)淀粉合酶II,也被称为淀粉颗粒蛋白1(SGP-1),在胚乳淀粉合成中起主要作用。三种SGP-1蛋白,即SGP-A1、B1和D1,由三个同源的SSII基因wSSII-A、B和D产生。先前已鉴定出携带每个SGP-1蛋白无效等位基因的品系。在本报告中,对每个wSSII基因中发生的突变进行了表征,并开发了能够检测这些突变的基于PCR的DNA标记。在无效的wSSII-A等位基因中,起始密码子附近存在一个289 bp的缺失,并伴有8 bp的填充DNA。在无效的wSSII-B等位基因的第8外显子中发生了一个175 bp的插入。该插入代表了一种最近发现的名为Hikkoshi的微型反向重复转座元件(MITE),它首次在小麦蜡质基因中被发现。在无效的wSSII-D等位基因的第五外显子和内含子交界处周围区域发现了一个63 bp的缺失。基于这些信息,我们设计了引物组,以便能够对每个位点进行等位基因特异性扩增。通过使用标记辅助选择重建一个缺乏所有三种SGP-1蛋白的品系,证明了这些引物组在育种计划中的适用性。这些标记对于旨在获得缺失一种或两种SGP-1蛋白的部分突变体的育种计划也将是有用的。