4.7 Article

Genome-wide identification and characterization of SnRK family genes in Brassica napus

Journal

BMC PLANT BIOLOGY
Volume 20, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12870-020-02484-3

Keywords

Brassica napus; SnRK; Genome-wide; Abiotic stress; Expression patterns

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Funding

  1. National Natural Science Foundation of China [31961143008, 31701411]
  2. Science and Technology Program of Zhejiang Province of China [LGN20C130007]
  3. Jiangsu Collaborative Innovation Center for Modern Crop Production
  4. 111 project for introduction of foreign experts [B17039]

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BackgroundSucrose non-fermenting 1 related protein kinases (SnRK) play crucial roles in responding to biotic and abiotic stresses through activating protein phosphorylation pathways. However, little information of SnRK genes was available in Brassica napus, one of important oil crops. Recently, the released sequences of the reference genome of B.napus provide a good chance to perform genome-wide identification and characterization of BnSnRK gene family in the rapeseed.ResultsTotally 114 SnRK genes distributed on 19 chromosomes were identified in the genome of B.napus and classified into three subfamilies on the basis of phylogenetic analysis and the domain types. According to gene structure and motif composition analysis, the BnSnRK sequences showed obvious divergence among three subfamilies. Gene duplication and synteny between the genomes of the rapeseed and Arabidopsis were also analyzed to provide insights into the evolutionary characteristics of BnSnRK family genes. Cis-element analysis revealed that BnSnRKs may response to diverse environmental stresses. Moreover, the expression patterns of BnSnRKs in various tissues and under diverse abiotic stresses were distinct difference. Besides, Single Nucleotide Polymorphisms (SNP) distribution analysis suggests the function disparity of BnSnRK family genes in different genotypes of the rapeseed.ConclusionWe examined genomic structures, evolution features, expression patterns and SNP distribution of 114 BnSnRKs. The results provide valuable information for functional characterization of BnSnRK genes in future studies.

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