Transcriptome analysis and identification of key genes involved in 1-deoxynojirimycin biosynthesis of mulberry (Morus alba L.)

被引:31
作者
Wang, Dujun [1 ,2 ]
Zhao, Li [3 ]
Wang, Dan [1 ]
Liu, Jia [1 ]
Yu, Xiaofeng [3 ]
Wei, Yuan [3 ]
Ouyang, Zhen [1 ,3 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang, Peoples R China
[2] Yancheng Inst Technol, Coll Oceanol & Bioengn, Yancheng, Peoples R China
[3] Jiangsu Univ, Sch Pharm, Zhenjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Mulberry; Transcriptomic; 1-deoxynojirimycin; Biosynthesis; Key enzyme gene analysis; ALPHA-AMINOADIPATE PATHWAY; LYSINE BIOSYNTHESIS; DIHYDRODIPICOLINATE SYNTHASE; ARABIDOPSIS-THALIANA; HIGHER-PLANTS; ACID; CLONING; DEHYDROGENASE; GENERATION; MORANOLINE;
D O I
10.7717/peerj.5443
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
Mulberry (Morus alba L.) represents one of the most commonly utilized plants in traditional medicine and as a nutritional plant used worldwide. The polyhydroxylated alkaloid 1-deoxynojirimycin (DNJ) is the major bioactive compounds of mulberry in treating diabetes. However, the DNJ content in mulberry is very low. Therefore, identification of key genes involved in DNJ alkaloid biosynthesis will provide a basis for the further analysis of its biosynthetic pathway and ultimately for the realization of synthetic biological production. Here, two cDNA libraries of mulberry leaf samples with different DNJ contents were constructed. Approximately 16 Gb raw RNA-Seq data was generated and de novo assembled into 112,481 transcripts, with an average length of 766 bp and an N50 value of 1,392. Subsequently, all unigenes were annotated based on nine public databases; 11,318 transcripts were found to be significantly differentially regulated. A total of 38 unique candidate genes were identified as being involved in DNJ alkaloid biosynthesis in mulberry, and nine unique genes had significantly different expression. Three key transcripts of DNJ biosynthesis were identified and further characterized using RT-PCR; they were assigned to lysine decarboxylase and primary-amine oxidase genes. Five CYP450 transcripts and two methyltransferase transcripts were significantly associated with DNJ content. Overall, the biosynthetic pathway of DNJ alkaloid was preliminarily speculated.
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页数:24
相关论文
共 62 条
[1]   Isoprenoid Pathway Optimization for Taxol Precursor Overproduction in Escherichia coli [J].
Ajikumar, Parayil Kumaran ;
Xiao, Wen-Hai ;
Tyo, Keith E. J. ;
Wang, Yong ;
Simeon, Fritz ;
Leonard, Effendi ;
Mucha, Oliver ;
Phon, Too Heng ;
Pfeifer, Blaine ;
Stephanopoulos, Gregory .
SCIENCE, 2010, 330 (6000) :70-74
[2]   Differential expression analysis for sequence count data [J].
Anders, Simon ;
Huber, Wolfgang .
GENOME BIOLOGY, 2010, 11 (10)
[3]   A large scale analysis of cDNA in Arabidopsis thaliana:: Generation of 12,028 non-redundant expressed sequence tags from normalized and size-selected cDNA libraries [J].
Asamizu, E ;
Nakamura, Y ;
Sato, S ;
Tabata, S .
DNA RESEARCH, 2000, 7 (03) :175-180
[4]   Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis [J].
Asano, N ;
Kato, A ;
Miyauchi, M ;
Kizu, H ;
Kameda, Y ;
Watson, AA ;
Nash, RJ ;
Fleet, GWJ .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (05) :625-628
[5]   ALPHA-AMINOADIPATE PATHWAY FOR THE BIOSYNTHESIS OF LYSINE IN LOWER EUKARYOTES [J].
BHATTACHARJEE, JK .
CRC CRITICAL REVIEWS IN MICROBIOLOGY, 1985, 12 (02) :131-151
[6]  
BLACK S, 1955, J BIOL CHEM, V213, P39
[7]   Practical syntheses of N-substituted 3-hydroxyazetidines and 4-hydroxypiperidines by hydroxylation with Sphingomonas sp HXN-200 [J].
Chang, DL ;
Feiten, HJ ;
Engesser, KH ;
van Beilen, JB ;
Witholt, B ;
Li, Z .
ORGANIC LETTERS, 2002, 4 (11) :1859-1862
[8]  
Chen ZuoYi Chen ZuoYi, 2013, China Journal of Traditional Chinese Medicine and Pharmacy, V28, P1815
[9]   Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: asymmetric synthesis of 1-deoxynojirimycin [J].
Comins, DL ;
Fulp, AB .
TETRAHEDRON LETTERS, 2001, 42 (39) :6839-6841
[10]  
CREMER J, 1988, J GEN MICROBIOL, V134, P3221