Qamar Zia-Ul-, Uzair Muhammad, Hameed Amjad, Zafar Syed Adeel, Li Xueyong
Plant Breeding & Genetics Division, Marker Assisted Breeding Group (MABG), Nuclear Institute for Agriculture and Biology (NIAB), Faisalabad, Pakistan.
State Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Front Plant Sci. 2024 Dec 17;15:1455219. doi: 10.3389/fpls.2024.1455219. eCollection 2024.
Low phytate level is a desirable trait because it promotes mineral bioavailability and thus offers a solution to tackle mineral deficiencies. The objectives of the present study were to characterize low phytate (lpa) Basmati rice mutants for the identification of novel mutations in target gene(s) and to develop a PCR-based CAPS (cleaved amplified polymorphic sequence) marker for low phytate Basmati rice. For this purpose, cultivar Super Basmati (Q4) was irradiated with gamma rays (Co source) and three mutants named Q1 (lpa-5-9), Q2 (lpa-9-13), and Q3 (lpa-59-14) were isolated. Four genes previously been reported for the low phytic acid trait in rice were sequenced in these mutants and no mutation was observed in Q1 and Q2. However, in Q3 (lpa14) mutant a novel mutation in gene () was detected. Sequence analysis displayed a substitution in the first exon of at position 1142 bp resulting in the amino acid change from glycine (Gly) to alanine (Ala) at position 381a.a. To facilitate low-phytate breeding program, CAPS marker was developed to confirm this mutation site using the restriction digestion by I restriction enzyme. After enzyme digestion, Q3 produces four bands (32, 220, 154, and 32 bp) while Q4 (parent cultivar Super Basmati) produces only 3 bands (32, 374, and 32 bp). These results showed that this CAPS marker is 100% linked with this mutation and can be used for future breeding programs. Present findings provided insights in molecular basis of low phytate trait in rice paving the way for developing low-phytate rice varieties through marker-assisted breeding.
低植酸水平是一个理想的性状,因为它能提高矿物质的生物利用率,从而为解决矿物质缺乏问题提供了一种解决方案。本研究的目的是对低植酸(lpa)巴斯马蒂水稻突变体进行表征,以鉴定目标基因中的新突变,并开发一种基于PCR的CAPS(酶切扩增多态性序列)标记用于低植酸巴斯马蒂水稻。为此,用伽马射线(钴源)辐照品种超级巴斯马蒂(Q4),并分离出三个突变体,分别命名为Q1(lpa-5-9)、Q2(lpa-9-13)和Q3(lpa-59-14)。对先前报道的与水稻低植酸性状相关的四个基因在这些突变体中进行测序,在Q1和Q2中未观察到突变。然而,在Q3(lpa14)突变体中检测到基因()的一个新突变。序列分析显示,在第1142 bp处的第一个外显子发生了替换,导致第381个氨基酸位置的甘氨酸(Gly)变为丙氨酸(Ala)。为了促进低植酸育种计划,开发了CAPS标记,使用I限制酶进行酶切来确认这个突变位点。酶切后,Q3产生四条带(32、220、154和32 bp),而Q4(亲本品种超级巴斯马蒂)只产生三条带(32、374和32 bp)。这些结果表明,这个CAPS标记与该突变100%连锁,可用于未来的育种计划。目前的研究结果为水稻低植酸性状的分子基础提供了见解,为通过标记辅助育种培育低植酸水稻品种铺平了道路。