Faculty of Agriculture, University of Zagreb, Svetošimunska Cesta 25, 10000 Zagreb, Croatia.
Centre of Excellence for Biodiversity and Molecular Plant Breeding (CroP-BioDiv), Svetošimunska Cesta 25, 10000 Zagreb, Croatia.
Genes (Basel). 2024 Aug 5;15(8):1028. doi: 10.3390/genes15081028.
Trypsin inhibitors (TI) in raw soybean grain, mainly represented by the Kunitz trypsin inhibitor protein (KTI), prevent the normal activity of the digestive enzymes trypsin and chymotrypsin in humans and monogastric livestock. The inactivation of TI is achieved through costly and time-consuming heat treatment. Thermal processing also impairs the solubility and availability of the soybean grain protein. Therefore, the genetic elimination of KTI has been proposed as a suitable alternative to heat treatment. The aim of this study was to screen the collection of European soybean cultivars with six genetic markers (one SSR marker and five SNP markers) previously proposed as tightly linked to the gene encoding the major Kunitz trypsin inhibitor seed protein of soybean and validate their usability for marker-assisted selection (MAS). The six markers were validated on a subset of 38 cultivars with wide variability in KTI content and in the F and F progenies of two crosses between the known high- and low-KTI cultivars. Three genetic markers (SSR Satt228 and two SNP markers, Gm08_45317135_T/G and Gm08_45541906_A/C) were significantly associated with KTI content in a subset of 38 cultivars. Low-KTI alleles were detected in both low- and high-KTI genotypes and vice versa, high-KTI alleles were found in both high- and low-KTI genotypes, indicating a tight but not perfect association of these markers with the gene. The genetic marker SSR Satt228 showed a significant association with KTI content in the F progeny, while the SNP markers Gm08_45317135_T/G and Gm08_45541906_A/C allowed significant discrimination between progeny with high- vs. low-KTI progenies in the F generation. These three markers could be applied in MAS for low-KTI content but not without the additional phenotyping step to extract the desired low-KTI genotypes.
Trypsin inhibitors (TI) in raw soybean grain, mainly represented by the Kunitz trypsin inhibitor protein (KTI), prevent the normal activity of the digestive enzymes trypsin and chymotrypsin in humans and monogastric livestock. The inactivation of TI is achieved through costly and time-consuming heat treatment. Thermal processing also impairs the solubility and availability of the soybean grain protein. Therefore, the genetic elimination of KTI has been proposed as a suitable alternative to heat treatment.
生大豆中的胰蛋白酶抑制剂(TI),主要由 Kunitz 胰蛋白酶抑制剂蛋白(KTI)组成,可阻止人和单胃家畜的消化酶胰蛋白酶和糜蛋白酶的正常活性。TI 的失活是通过昂贵且耗时的热处理来实现的。热处理还会损害大豆蛋白的溶解度和可用性。因此,已经提出了基因消除 KTI 作为热处理的合适替代方法。
The aim of this study was to screen the collection of European soybean cultivars with six genetic markers (one SSR marker and five SNP markers) previously proposed as tightly linked to the gene encoding the major Kunitz trypsin inhibitor seed protein of soybean and validate their usability for marker-assisted selection (MAS).
本研究的目的是筛选具有六个遗传标记(一个 SSR 标记和五个 SNP 标记)的欧洲大豆品种,这些标记先前被提议与编码大豆主要 Kunitz 胰蛋白酶抑制剂种子蛋白的 基因紧密连锁,并验证它们在标记辅助选择(MAS)中的可用性。
The six markers were validated on a subset of 38 cultivars with wide variability in KTI content and in the F and F progenies of two crosses between the known high- and low-KTI cultivars.
在 KTI 含量差异较大的 38 个品种亚组以及已知高 KTI 和低 KTI 品种之间的两个杂交 F 和 F 后代中,对这六个标记进行了验证。
Three genetic markers (SSR Satt228 and two SNP markers, Gm08_45317135_T/G and Gm08_45541906_A/C) were significantly associated with KTI content in a subset of 38 cultivars.
在 38 个品种的亚组中,有三个遗传标记(SSR Satt228 和两个 SNP 标记,Gm08_45317135_T/G 和 Gm08_45541906_A/C)与 KTI 含量显著相关。
Low-KTI alleles were detected in both low- and high-KTI genotypes and vice versa, high-KTI alleles were found in both high- and low-KTI genotypes, indicating a tight but not perfect association of these markers with the gene.
在低 KTI 和高 KTI 基因型中都检测到低 KTI 等位基因,反之亦然,在高 KTI 和低 KTI 基因型中都发现了高 KTI 等位基因,表明这些标记与 基因的紧密但非完美关联。
The genetic marker SSR Satt228 showed a significant association with KTI content in the F progeny, while the SNP markers Gm08_45317135_T/G and Gm08_45541906_A/C allowed significant discrimination between progeny with high- vs. low-KTI progenies in the F generation.
遗传标记 SSR Satt228 与 F 代的 KTI 含量显著相关,而 SNP 标记 Gm08_45317135_T/G 和 Gm08_45541906_A/C 允许在 F 代高 KTI 与低 KTI 后代之间进行显著区分。
These three markers could be applied in MAS for low-KTI content but not without the additional phenotyping step to extract the desired low-KTI genotypes.
这三个标记可用于 MAS 中的低 KTI 含量,但如果不进行额外的表型鉴定步骤以提取所需的低 KTI 基因型,则无法应用。