Literature DB >> 18563445

Recent duplications dominate NBS-encoding gene expansion in two woody species.

Sihai Yang1, Xiaohui Zhang, Jia-Xing Yue, Dacheng Tian, Jian-Qun Chen.   

Abstract

Most disease resistance genes in plants encode NBS-LRR proteins. However, in woody species, little is known about the evolutionary history of these genes. Here, we identified 459 and 330 respective NBS-LRRs in grapevine and poplar genomes. We subsequently investigated protein motif composition, phylogenetic relationships and physical locations. We found significant excesses of recent duplications in perennial species, compared with those of annuals, represented by rice and Arabidopsis. Consequently, we observed higher nucleotide identity among paralogs and a higher percentage of NBS-encoding genes positioned in numerous clusters in the grapevine and poplar. These results suggested that recent tandem duplication played a major role in NBS-encoding gene expansion in perennial species. These duplication events, together with a higher probability of recombination revealed in this study, could compensate for the longer generation time in woody perennial species e.g. duplication and recombination could serve to generate novel resistance specificities. In addition, we observed extensive species-specific expansion in TIR-NBS-encoding genes. Non-TIR-NBS-encoding genes were poly- or paraphyletic, i.e. genes from three or more plant species were nested in different clades, suggesting different evolutionary patterns between these two gene types.

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Year:  2008        PMID: 18563445     DOI: 10.1007/s00438-008-0355-0

Source DB:  PubMed          Journal:  Mol Genet Genomics        ISSN: 1617-4623            Impact factor:   3.291


  38 in total

1.  Plant disease resistance genes encode members of an ancient and diverse protein family within the nucleotide-binding superfamily.

Authors:  B C Meyers; A W Dickerman; R W Michelmore; S Sivaramakrishnan; B W Sobral; N D Young
Journal:  Plant J       Date:  1999-11       Impact factor: 6.417

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Journal:  Science       Date:  2001-01-05       Impact factor: 47.728

Review 3.  The arms race is ancient history in Arabidopsis, the wildflower.

Authors:  E B Holub
Journal:  Nat Rev Genet       Date:  2001-07       Impact factor: 53.242

Review 4.  Structure and function of resistance proteins in solanaceous plants.

Authors:  Gerben van Ooijen; Harrold A van den Burg; Ben J C Cornelissen; Frank L W Takken
Journal:  Annu Rev Phytopathol       Date:  2007       Impact factor: 13.078

Review 5.  Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions.

Authors:  Andrew F Bent; David Mackey
Journal:  Annu Rev Phytopathol       Date:  2007       Impact factor: 13.078

Review 6.  Clusters of resistance genes in plants evolve by divergent selection and a birth-and-death process.

Authors:  R W Michelmore; B C Meyers
Journal:  Genome Res       Date:  1998-11       Impact factor: 9.043

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Authors:  Kan Nobuta; Tom Ashfield; Sun Kim; Roger W Innes
Journal:  Mol Plant Microbe Interact       Date:  2005-02       Impact factor: 4.171

8.  Genome-wide investigation on the genetic variations of rice disease resistance genes.

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9.  Genome-wide identification of NBS genes in japonica rice reveals significant expansion of divergent non-TIR NBS-LRR genes.

Authors:  T Zhou; Y Wang; J-Q Chen; H Araki; Z Jing; K Jiang; J Shen; D Tian
Journal:  Mol Genet Genomics       Date:  2004-03-10       Impact factor: 3.291

10.  The sequence of rice chromosomes 11 and 12, rich in disease resistance genes and recent gene duplications.

Authors: 
Journal:  BMC Biol       Date:  2005-09-27       Impact factor: 7.431

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  180 in total

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3.  Relative evolutionary rates of NBS-encoding genes revealed by soybean segmental duplication.

Authors:  Xiaohui Zhang; Ying Feng; Hao Cheng; Dacheng Tian; Sihai Yang; Jian-Qun Chen
Journal:  Mol Genet Genomics       Date:  2010-11-16       Impact factor: 3.291

4.  Large-Scale Analyses of Angiosperm Nucleotide-Binding Site-Leucine-Rich Repeat Genes Reveal Three Anciently Diverged Classes with Distinct Evolutionary Patterns.

Authors:  Zhu-Qing Shao; Jia-Yu Xue; Ping Wu; Yan-Mei Zhang; Yue Wu; Yue-Yu Hang; Bin Wang; Jian-Qun Chen
Journal:  Plant Physiol       Date:  2016-02-02       Impact factor: 8.340

5.  The F-box family genes as key elements in response to salt, heavy mental, and drought stresses in Medicago truncatula.

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Journal:  Funct Integr Genomics       Date:  2015-04-16       Impact factor: 3.410

6.  Functional identification and regulation of the PtDrl02 gene promoter from triploid white poplar.

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Journal:  Plant Cell Rep       Date:  2010-02-24       Impact factor: 4.570

7.  Identification and characterization of the SET domain gene family in maize.

Authors:  Yexiong Qian; Yilong Xi; Beijiu Cheng; Suwen Zhu; Xianzhao Kan
Journal:  Mol Biol Rep       Date:  2014-01-04       Impact factor: 2.316

8.  Genome-wide identification of barley MCs (metacaspases) and their possible roles in boron-induced programmed cell death.

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Journal:  Mol Biol Rep       Date:  2018-02-05       Impact factor: 2.316

9.  A significant fraction of 21-nucleotide small RNA originates from phased degradation of resistance genes in several perennial species.

Authors:  Thomas Källman; Jun Chen; Niclas Gyllenstrand; Ulf Lagercrantz
Journal:  Plant Physiol       Date:  2013-04-11       Impact factor: 8.340

Review 10.  Plant STAND P-loop NTPases: a current perspective of genome distribution, evolution, and function : Plant STAND P-loop NTPases: genomic organization, evolution, and molecular mechanism models contribute broadly to plant pathogen defense.

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Journal:  Mol Genet Genomics       Date:  2017-09-12       Impact factor: 3.291

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