SNP in Chalcone Synthase gene is associated with variation of 6-gingerol content in contrasting landraces of Zingiber officinale.Roscoe

被引:6
作者
Ghosh, Subhabrata [1 ]
Sen Mandi, Swati [1 ]
机构
[1] Bose Inst, Div Plant Biol, Kolkata, India
关键词
Zingiber officinale; 6-Gingerol; Chalcone synthase; Differential gene expression; Single nucleotide polymorphism; Active site alteration; EXPRESSION;
D O I
10.1016/j.gene.2015.04.042
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Zingiber officinale, medicinally the most important species within Zingiber genus, contains 6-gingerol as the active principle. This compound obtained from rhizomes of Z.officinale, has immense medicinal importance and is used in various herbal drug formulations. Our record of variation in content of this active principle, viz. 6-gingerol, in land races of this drug plant collected from different locations correlated with our Gene expression studies exhibiting high Chalcone Synthase gene (Chalcone Synthase is the rate limiting enzyme of 6-gingerol biosynthesis pathway) expression in high 6-gingerol containing landraces than in the low 6-gingerol containing landraces. Sequencing of Chalcone Synthase cDNA and subsequent multiple sequence alignment revealed seven SNPs between these contrasting genotypes. Converting this nucleotide sequence to amino acid sequence, alteration of two amino acids becomes evident; one amino acid change (asparagine to serine at position 336) is associated with base change (A -> G) and another change (serine to leucine at position 142) is associated with the base change (C -> T). Since asparagine at position 336 is one of the critical amino acids of the catalytic triad of Chalcone Synthase enzyme, responsible for substrate binding, our study suggests that landraces with a specific amino acid change viz. Asparagine (found in high 6-gingerol containing landraces) to serine causes low 6-gingerol content This is probably due to a weak enzyme substrate association caused by the absence of asparagine in the catalytic triad. Detailed study of this finding could also help to understand molecular mechanism associated with variation in 6-gingerol content in Z.officinale genotypes and thereby strategies for developing elite genotypes containing high 6-gingerol content. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 188
页数:5
相关论文
共 19 条
[1]  
Acala J., 1997, MOL BREEDING, V3, P495
[2]  
[Anonymous], 1989, Cold Spring Harbor
[3]   The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling [J].
Arnold, K ;
Bordoli, L ;
Kopp, J ;
Schwede, T .
BIOINFORMATICS, 2006, 22 (02) :195-201
[4]   Microsatellites and a single-nucleotide polymorphism differentiate apparent amylose classes in an extended pedigree of US rice germ plasm [J].
Ayres, NM ;
McClung, AM ;
Larkin, PD ;
Bligh, HFJ ;
Jones, CA ;
Park, WD .
THEORETICAL AND APPLIED GENETICS, 1997, 94 (6-7) :773-781
[5]  
Chiapparino E., 2003, P PLANT AN GEN 11 C
[6]  
Ellis M., 2005, THEOR APPL GENET, V105, P1038
[7]  
Ferrer J. L., 1999, GENE, V225, P127
[8]  
GOVINDARAJAN VS, 1982, CRC CR REV FOOD SCI, V17, P1
[9]   Molecular tagging of erucic acid trait in oilseed mustard (Brassica juncea) by QTL mapping and single nucleotide polymorphisms in FAE1 gene [J].
Gupta, V ;
Mukhopadhyay, A ;
Arumugam, N ;
Sodhi, YS ;
Pental, D ;
Pradhan, AK .
THEORETICAL AND APPLIED GENETICS, 2004, 108 (04) :743-749
[10]   Development of SNP assays for genotyping the puroindoline b gene for grain hardness in wheat using pyrosequencing [J].
Huang, XQ ;
Röder, MS .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (06) :2070-2075