Novel allelic variant of Lpa1 gene associated with a significant reduction in seed phytic acid content in rice (Oryza sativa L.)

被引:14
|
作者
Kishor, D. S. [1 ,2 ]
Lee, Choonseok [1 ,2 ]
Lee, Dongryung [1 ,2 ]
Venkatesh, Jelli [1 ,2 ]
Seo, Jeonghwan [1 ,2 ]
Chin, Joong Hyoun [3 ]
Jin, Zhuo [1 ,2 ]
Hong, Soon-Kwan [4 ]
Ham, Jin-Kwan [5 ]
Koh, Hee Jong [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Plant Sci, Plant Genom & Breeding Inst, Seoul, South Korea
[2] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul, South Korea
[3] Sejong Univ, Grad Sch Integrated Bioind, Seoul, South Korea
[4] Kangwon Natl Univ, Div Biotechnol, Chunchon, Gangwon Do, South Korea
[5] Gangwon Prov Agr Res & Extens Serv, Chunchon, Gangwon Do, South Korea
来源
PLOS ONE | 2019年 / 14卷 / 03期
关键词
LOW-PHYTATE MUTATIONS; MYO-INOSITOL-1-PHOSPHATE SYNTHASE; MOLECULAR CHARACTERIZATION; GRAIN-YIELD; MAIZE; PHOSPHORYLATION; IDENTIFICATION; PHOSPHORUS; KINASE; ACCUMULATION;
D O I
10.1371/journal.pone.0209636
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In plants, myo-inositol-1,2,3,4,5,6-hexakisphosphate (InsP(6)), also known as phytic acid (PA), is a major component of organic phosphorus (P), and accounts for up to 85% of the total P in seeds. In rice (Oryza sativa L.), PA mainly accumulates in rice bran, and chelates mineral cations, resulting in mineral deficiencies among brown rice consumers. Therefore, considerable efforts have been focused on the development of low PA (LPA) rice cultivars. In this study, we performed genetic and molecular analyses of OsLpa1, a major PA biosynthesis gene, in Sanggol, a low PA mutant variety developed via chemical mutagenesis of Ilpum rice cultivar. Genetic segregation and sequencing analyses revealed that a recessive allele, lpa1-3, at the OsLpa1 locus (Os02g0819400) was responsible for a significant reduction in seed PA content in Sanggol. The lpa1-3 gene harboured a point mutation (C623T) in the fourth exon of the predicted coding region, resulting in threonine (Thr) to isoleucine (Ile) amino acidsubstitution at position 208 (Thr208Ile). Three-dimensional analysis of Lpa1 protein structure indicated that myo-inositol 3-monophosphate [Ins(3)P-1] could bind to the active site of Lpa1, with ATP as a cofactor for catalysis. Furthermore, the presence of Thr208 in the loop adjacent to the entry site of the binding pocket suggests that Thr208Ile substitution is involved in regulating enzyme activity via phosphorylation. Therefore, we propose that Thr208Ile substitution in lpa1-3 reduces Lpa1 enzyme activity in Sanggol, resulting in reduced PA biosynthesis.
引用
收藏
页数:20
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