Genome-wide analysis of NBS-LRR genes revealed contribution of disease resistance from Saccharum spontaneum to modern sugarcane cultivar

被引:5
作者
Jiang, Zhengjie [1 ]
Zhao, Mengyu [1 ]
Qin, Hongzhen [2 ]
Li, Sicheng [1 ]
Yang, Xiping [1 ,2 ]
机构
[1] Guangxi Univ, State Key Lab Conservat & Utilizat Subtrop Agrobio, Guangxi Key Lab Sugarcane Biol, Nanning, Peoples R China
[2] Guangxi Univ, Coll Agr, Natl Demonstrat Ctr Expt Plant Sci Educ, Nanning, Peoples R China
来源
FRONTIERS IN PLANT SCIENCE | 2023年 / 14卷
基金
中国国家自然科学基金;
关键词
sugarcane; NBS-LRR genes; phylogenetic analysis; evolutionary analyses; transcriptomic analysis; DIFFERENTIAL EXPRESSION ANALYSIS; ALLELE-SPECIFIC EXPRESSION; CONFERS RESISTANCE; PLANT; EVOLUTION; SEQUENCE; DUPLICATION; RECOGNITION; MUTATIONS; PATHOGENS;
D O I
10.3389/fpls.2023.1091567
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
IntroductionDuring plant evolution, nucleotide-binding sites (NBS) and leucine-rich repeat (LRR) genes have made significant contributions to plant disease resistance. With many high-quality plant genomes sequenced, identification and comprehensive analyses of NBS-LRR genes at whole genome level are of great importance to understand and utilize them. MethodsIn this study, we identified the NBS-LRR genes of 23 representative species at whole genome level, and researches on NBS-LRR genes of four monocotyledonous grass species, Saccharum spontaneum, Saccharum officinarum, Sorghum bicolor and Miscanthus sinensis, were focused. Results and discussionWe found that whole genome duplication, gene expansion, and allele loss could be factors affecting the number of NBS-LRR genes in the species, and whole genome duplication is likely to be the main cause of the number of NBS-LRR genes in sugarcane. Meanwhile, we also found a progressive trend of positive selection on NBS-LRR genes. These studies further elucidated the evolutionary pattern of NBS-LRR genes in plants. Transcriptome data from multiple sugarcane diseases revealed that more differentially expressed NBS-LRR genes were derived from S. spontaneum than from S. officinarum in modern sugarcane cultivars, and the proportion was significantly higher than the expected. This finding reveals that S. spontaneum has a greater contribution to disease resistance for modern sugarcane cultivars. In addition, we observed allelespecific expression of seven NBS-LRR genes under leaf scald, and 125 NBS-LRR genes responding to multiple diseases were identified. Finally, we built a plant NBS-LRR gene database to facilitate subsequent analysis and use of NBSLRR genes obtained here. In conclusion, this study complemented and completed the research of plant NBS-LRR genes, and discussed how NBS-LRR genes responding to sugarcane diseases, which provided a guide and genetic resources for further research and utilization of NBS-LRR genes.
引用
收藏
页数:12
相关论文
共 67 条
[41]   Understanding the functions of plant disease resistance proteins [J].
Martin, GB ;
Bogdanove, AJ ;
Sessa, G .
ANNUAL REVIEW OF PLANT BIOLOGY, 2003, 54 :23-61
[42]   Plant NBS-LRR proteins: adaptable guards [J].
McHale, Leah ;
Tan, Xiaoping ;
Koehl, Patrice ;
Michelmore, Richard W. .
GENOME BIOLOGY, 2006, 7 (04)
[43]   Plant disease resistance genes encode members of an ancient and diverse protein family within the nucleotide-binding superfamily [J].
Meyers, BC ;
Dickerman, AW ;
Michelmore, RW ;
Sivaramakrishnan, S ;
Sobral, BW ;
Young, ND .
PLANT JOURNAL, 1999, 20 (03) :317-332
[44]   The Wheat Lr67 Gene from the Sugar Transport Protein 13 Family Confers Multipathogen Resistance in Barley [J].
Milne, Ricky J. ;
Dibley, Katherine E. ;
Schnippenkoetter, Wendelin ;
Mascher, Martin ;
Lui, Andy C. W. ;
Wang, Lanxiang ;
Lo, Clive ;
Ashton, Anthony R. ;
Ryan, Peter R. ;
Lagudah, Evans S. .
PLANT PHYSIOLOGY, 2019, 179 (04) :1285-1297
[45]   A recently evolved hexose transporter variant confers resistance to multiple pathogens in wheat [J].
Moore, John W. ;
Herrera-Foessel, Sybil ;
Lan, Caixia ;
Schnippenkoetter, Wendelin ;
Ayliffe, Michael ;
Huerta-Espino, Julio ;
Lillemo, Morten ;
Viccars, Libby ;
Milne, Ricky ;
Periyannan, Sambasivam ;
Kong, Xiuying ;
Spielmeyer, Wolfgang ;
Talbot, Mark ;
Bariana, Harbans ;
Patrick, John W. ;
Dodds, Peter ;
Singh, Ravi ;
Lagudah, Evans .
NATURE GENETICS, 2015, 47 (12) :1494-1498
[46]   Recognition and response in the plant immune system [J].
Nimchuk, Z ;
Eulgem, T ;
Holt, BE ;
Dangl, JL .
ANNUAL REVIEW OF GENETICS, 2003, 37 :579-609
[47]   Salmon provides fast and bias-aware quantification of transcript expression [J].
Patro, Rob ;
Duggal, Geet ;
Love, Michael I. ;
Irizarry, Rafael A. ;
Kingsford, Carl .
NATURE METHODS, 2017, 14 (04) :417-+
[48]   The formation and function of plant volatiles: perfumes for pollinator attraction and defense [J].
Pichersky, E ;
Gershenzon, J .
CURRENT OPINION IN PLANT BIOLOGY, 2002, 5 (03) :237-243
[49]   edgeR: a Bioconductor package for differential expression analysis of digital gene expression data [J].
Robinson, Mark D. ;
McCarthy, Davis J. ;
Smyth, Gordon K. .
BIOINFORMATICS, 2010, 26 (01) :139-140
[50]   Revisiting the Origin of Plant NBS-LRR Genes [J].
Shao, Zhu-Qing ;
Xue, Jia-Yu ;
Wang, Qiang ;
Wang, Bin ;
Chen, Jian-Qun .
TRENDS IN PLANT SCIENCE, 2019, 24 (01) :9-12