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Mutations in wheat starch synthase II genes and PCR-based selection of a SGP-1 null line
Authors:T. Shimbata  T. Nakamura  P. Vrinten  M. Saito  J. Yonemaru  Y. Seto  H. Yasuda
Affiliation:(1) Central Laboratory, Nippon Flour Mills Co. Ltd., 5-1-3 Midorigaoka, Atsugi, Kanagawa, Japan;(2) Tohoku National Agriculture Research Center, 4 Akahira, Shimo-Kuriyagawa, Morioka Iwate, 020-0198, Japan;(3) Present address: Bioriginal Food& Science Corp, 102 Melville Street, Saskatoon, Saskatchewan, S7J 0R1, Canada
Abstract: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.
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