W952631 小麦族中串联重复 DNA 序列家系的鉴定[刊,英]/Vershinin,A.…//Theoretical and Ap-plied Genetics.-1994,89(2/3).-217～225W952632 高等植物线粒体 DNA 中的保守序列和新基因的检测[著,英]/Lejeune,B.…//Plant mito-chondri...W952631 小麦族中串联重复 DNA 序列家系的鉴定[刊,英]/Vershinin,A.…//Theoretical and Ap-plied Genetics.-1994,89(2/3).-217～225W952632 高等植物线粒体 DNA 中的保守序列和新基因的检测[著,英]/Lejeune,B.…//Plant mito-chondria:with emphasis on RNA editing and cyto-plasmic male sterility/Brennicke,A.….-Weinheim,Germany:VCH Verlagsgesellschaft mbH,1993.-145～149.-ISBN 3-527-30033-3[WBTA,1994,11(5),4246]展开更多
The class of nucleotide-binding site(NBS)-Leucine-rich repeat(LRR) disease resistance genes play an important role in defending plants from a variety of pathogens and insect pests. Consequently, many NBS-LRR genes hav...The class of nucleotide-binding site(NBS)-Leucine-rich repeat(LRR) disease resistance genes play an important role in defending plants from a variety of pathogens and insect pests. Consequently, many NBS-LRR genes have been identified in various plant species. In this study, we identified 617 NBS-encoding genes in the Medicago truncatula genome(Mt3.5v5) and divided them into two groups, regular(490) and non-regular(127) NBSLRR genes. The regular NBS-LRR genes were characterized on the bases of structural diversity, chromosomal location, gene duplication, conserved protein motifs, and EST expression profiling. According to N-terminal motifs and LRR motifs, the 490 regular NBS-LRR genes were then classified into 10 types: CC-NBS(4), CC-NBS-LRR(212), TIR-NBS(20), TIR-NBS-LRR(160), TIR-NBS-TIR(1), TIR-NBS-TIR-LRR(2), NBS-TIR(7), NBS-TIR-LRR(1), NBS(10), and NBS-LRR(73). Analysis of the physical location and duplications of the regular NBS-LRR genes revealed that the M. truncatula genome is similar to rice. Interestingly, we found that TIR-type genes are more frequently expressed than non-TIR-type genes in M. truncatula, whereas the number of non-TIR-type regular NBSLRR genes was greater than TIR-type genes, suggesting the gene expression was not associated with the total number of NBS-LRR genes. Moreover, we found that the phylogenetic tree supported our division of the regular NBS-LRR genes into two distinct clades(TIR-type and non-TIR-type), but some of the non-TIR-type lineages contain TIR-type genes. These analyses provide a robust database of NBS-LRR genes in M. truncatula that will facilitate the isolation of new resistance genes and breeding strategies to engineer disease resistance in leguminous crop.展开更多
文摘W952631 小麦族中串联重复 DNA 序列家系的鉴定[刊,英]/Vershinin,A.…//Theoretical and Ap-plied Genetics.-1994,89(2/3).-217～225W952632 高等植物线粒体 DNA 中的保守序列和新基因的检测[著,英]/Lejeune,B.…//Plant mito-chondria:with emphasis on RNA editing and cyto-plasmic male sterility/Brennicke,A.….-Weinheim,Germany:VCH Verlagsgesellschaft mbH,1993.-145～149.-ISBN 3-527-30033-3[WBTA,1994,11(5),4246]
基金supported by the National Basic Research Program of China(2014CB138702)
文摘The class of nucleotide-binding site(NBS)-Leucine-rich repeat(LRR) disease resistance genes play an important role in defending plants from a variety of pathogens and insect pests. Consequently, many NBS-LRR genes have been identified in various plant species. In this study, we identified 617 NBS-encoding genes in the Medicago truncatula genome(Mt3.5v5) and divided them into two groups, regular(490) and non-regular(127) NBSLRR genes. The regular NBS-LRR genes were characterized on the bases of structural diversity, chromosomal location, gene duplication, conserved protein motifs, and EST expression profiling. According to N-terminal motifs and LRR motifs, the 490 regular NBS-LRR genes were then classified into 10 types: CC-NBS(4), CC-NBS-LRR(212), TIR-NBS(20), TIR-NBS-LRR(160), TIR-NBS-TIR(1), TIR-NBS-TIR-LRR(2), NBS-TIR(7), NBS-TIR-LRR(1), NBS(10), and NBS-LRR(73). Analysis of the physical location and duplications of the regular NBS-LRR genes revealed that the M. truncatula genome is similar to rice. Interestingly, we found that TIR-type genes are more frequently expressed than non-TIR-type genes in M. truncatula, whereas the number of non-TIR-type regular NBSLRR genes was greater than TIR-type genes, suggesting the gene expression was not associated with the total number of NBS-LRR genes. Moreover, we found that the phylogenetic tree supported our division of the regular NBS-LRR genes into two distinct clades(TIR-type and non-TIR-type), but some of the non-TIR-type lineages contain TIR-type genes. These analyses provide a robust database of NBS-LRR genes in M. truncatula that will facilitate the isolation of new resistance genes and breeding strategies to engineer disease resistance in leguminous crop.
