Genome-wide investigation and expression analyses of the pentatricopeptide repeat protein gene family in foxtail millet

被引:29
|
作者
Liu, Jia-Ming [1 ,2 ]
Xu, Zhao-Shi [1 ]
Lu, Pan-Pan [1 ]
Li, Wei-Wei [1 ,2 ]
Chen, Ming [1 ]
Guo, Chang-Hong [2 ]
Ma, You-Zhi [1 ]
机构
[1] Chinese Acad Agr Sci, Natl Key Facil Crop Gene Resources & Genet Improv, Key Lab Biol & Genet Improvement Triticeae Crops, Inst Crop Sci,Minist Agr, Beijing 100081, Peoples R China
[2] Harbin Normal Univ, Coll Life Sci & Technol, Key Lab Mol Cytogenet & Genet Breeding Heilongjia, Harbin 150025, Peoples R China
来源
BMC GENOMICS | 2016年 / 17卷
基金
中国国家自然科学基金;
关键词
Foxtail millet; Pentatricopeptide repeat (PPR) proteins; Genome segmental duplication; Phylogenesis; Responsive mechanism; Subcellular localization; ABSCISIC-ACID; PPR PROTEINS; ARABIDOPSIS-THALIANA; SEED DEVELOPMENT; SETARIA-ITALICA; MOTIF PROTEIN; MITOCHONDRIAL; SEQUENCE; RICE; IDENTIFICATION;
D O I
10.1186/s12864-016-3184-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Pentatricopeptide repeat (PPR) proteins are encoded by a large gene family of approximately 450 members in Arabidopsis and 477 in rice, which characterized by tandem repetitions of a degenerate 35 amino acid characteristic sequence motifs. A large majority of the PPR genes in the higher plants are localized in organelles. Their functions remain as yet largely unknown. The majority of characterized PPR proteins have been found to function in modulating the expression plastid and mitochondrial genes in plants. Results: Here, a genome-wide identification and comparison of the PPR genes from 5 organisms was performed, including the moss Physcomitrella patens, the lycophyte Selaginella moellendorffii, the eudicot Arabidopsis, and the monocots rice and foxtail millet. It appears that the expansion of this gene family prior to the divergence of the euphyllophytes and the lycophytes in land plants. The duplication and divergence rates of the foxtail millet PPR genes (SiPPRs) showed that the expansion period of this gene family around 400 Mya, and indicated that genome segmental duplication was very likely the primary mechanism underlying the expansion of the PPR gene family in vascular plants. An analysis of a complete set of SiPPR genes/proteins that included classification, chromosomal location, orthologous relationships, duplication analysis, and auxiliary motifs is presented. Expression analysis of the SiPPR genes under stress conditions revealed that the expression of 24 SiPPR genes was responsive to abiotic stress. Subcellular localization analysis of 11 PPR proteins indicated that 5 proteins were localized to chloroplasts, that 4 were localized to mitochondria, and that 2 were localized to the cytoplasm. Conclusions: Our results contribute to a more comprehensive understanding the roles of PPR proteins and will be useful in the prioritization of particular PPR proteins for subsequent functional validation studies in foxtail millet.
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页数:16
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