4.7 Article

Genome-Wide Identification, Characterization and Expression Profiling of Aluminum-Activated Malate Transporters in Eriobotrya japonica Lindl.

期刊

HORTICULTURAE
卷 7, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/horticulturae7110441

关键词

gene duplication; ALMT; synteny; malic acid; conserved motif; cis-regulatory elements

资金

  1. Plant Biological Seedling Science and Technology Innovation Team [CXTD2021009-03]
  2. Enterprise Technology Development [2020-3501-04-001995]

向作者/读者索取更多资源

This study systematically characterized the ALMT gene family in loquat and showed their potential roles in plant metabolism, including regulation of organic acids in fruits, movement of guard cells, and inducing tolerance against aluminum stress. Bioinformatics analysis revealed the conservation of ALMT superfamily domain in EjALMT proteins, which were predicted to be localized in the plasma membrane. The findings of genomic structural analysis, motif analysis, and syntenic analysis indicated the crucial role of duplication events in expanding the EjALMT gene family. The expression analysis identified differential gene expression in different loquat tissues, suggesting their diverse roles in plant growth and development.
Aluminum-activated malate transporters (ALMTs) have multiple potential roles in plant metabolism such as regulation of organic acids in fruits, movement of guard cells and inducing tolerance against aluminum stress. However, the systematic characterization of ALMT genes in loquat is yet to be performed. In the current study, 24 putative ALMT genes were identified in the genome of Eriobotrya japonica Lindl. To further investigate the role of those ALMT genes, comprehensive bioinformatics and expression analysis were performed. In bioinformatics analysis, the physiochemical properties, conserved domains, gene structure, conserved motif, phylogenetic and syntenic analysis of EjALMT genes were conducted. The result revealed that the ALMT superfamily domain was conserved in all EjALMT proteins. EjALMT proteins were predicted to be localized in the plasma membrane. Genomic structural and motif analysis showed that the exon and motif number of each EjALMT gene ranged dramatically, from 5 to 7, and 6 to 10, respectively. Syntenic analysis indicated that the segmental or whole-genome duplication played a vital role in extension of the EjALMT gene family. The K-a and K-s values of duplicated genes depicted that EjALMT genes have undergone a strong purifying selection. Furthermore, the expression analysis of EjALMT genes was performed in the root, mature leaf, stem, full-bloom flower and ripened fruit of loquat. Some genes were expressed differentially in examined loquat tissues, signifying their differential role in plant growth and development. This study provides the first genome-wide identification, characterization, and relative expression of the ALMT gene family in loquat and provides the foundation for further functional analysis.

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