Genome-Wide Comparison and Functional Characterization of HMGR Gene Family Associated with Shikonin Biosynthesis in Lithospermum erythrorhizon

被引:6
|
作者
Wang, Xuan [1 ,2 ]
Wang, Changyi [1 ,2 ]
Yang, Minkai [1 ,2 ]
Jie, Wencai [1 ]
Fazal, Aliya [1 ]
Fu, Jiangyan [1 ]
Yin, Tongming [2 ]
Cai, Jinfeng [2 ]
Liu, Bao [3 ]
Lu, Guihua [1 ,4 ]
Lin, Hongyan [1 ]
Han, Hongwei [1 ,2 ]
Wen, Zhongling [1 ,2 ]
Qi, Jinliang [1 ,2 ]
Yang, Yonghua [1 ,2 ]
机构
[1] Nanjing Univ, Sch Life Sci, Inst Plant Mol Biol, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Forestry Univ, Coinnovat Ctr Sustainable Forestry Southern China, Nanjing 210037, Peoples R China
[3] Northeast Normal Univ, Minist Educ MOE, Key Lab Mol Epigenet, Changchun 130024, Peoples R China
[4] Huaiyin Normal Univ, Sch Life Sci, Huaian 223300, Peoples R China
基金
中国国家自然科学基金;
关键词
duplication and loss; evolutionary; enzymatic activities; HMGR; Lithospermum erythrorhizon; COENZYME-A REDUCTASE; SUSPENSION-CULTURES; COA REDUCTASE; GERANYLTRANSFERASE; DIPHOSPHATE; DERIVATIVES; EXPRESSION; EXTRACTS; CLONING; INTRON;
D O I
10.3390/ijms241512532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3-hydroxy-3-methylglutaryl-CoA reductase (HMGR), as the rate-limiting enzyme in the mevalonate pathway, is essential for the biosynthesis of shikonin in Lithospermum erythrorhizon. However, in the absence of sufficient data, the principles of a genome-wide in-depth evolutionary exploration of HMGR family members in plants, as well as key members related to shikonin biosynthesis, remain unidentified. In this study, 124 HMGRs were identified and characterized from 36 representative plants, including L. erythrorhizon. Vascular plants were found to have more HMGR family genes than nonvascular plants. The phylogenetic tree revealed that during lineage and species diversification, the HMGRs evolved independently and intronless LerHMGRs emerged from multi-intron HMGR in land plants. Among them, Pinus tabuliformis and L. erythrorhizon had the most HMGR gene duplications, with 11 LerHMGRs most likely expanded through WGD/segmental and tandem duplications. In seedling roots and M9 cultured cells/hairy roots, where shikonin biosynthesis occurs, LerHMGR1 and LerHMGR2 were expressed significantly more than other genes. The enzymatic activities of LerHMGR1 and LerHMGR2 further supported their roles in catalyzing the conversion of HMG-CoA to mevalonate. Our findings provide insight into the molecular evolutionary properties and function of the HMGR family in plants and a basis for the genetic improvement of efficiently produced secondary metabolites in L. erythrorhizon.
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收藏
页数:17
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