Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca

被引:3
|
作者
Huang, Xiaolong [1 ,2 ,3 ]
Sun, Guilian [1 ,2 ,3 ]
Wu, Zongmin [1 ,2 ,3 ]
Jiang, Yu [1 ]
Li, Qiaohong [4 ]
Yi, Yin [1 ,2 ,3 ]
Yan, Huiqing [1 ]
机构
[1] Guizhou Normal Univ, Sch Life Sci, Guiyang 550001, Peoples R China
[2] Guizhou Normal Univ, Key Lab Plant Physiol & Dev Regulat, Guiyang 550001, Peoples R China
[3] Guizhou Normal Univ, Key Lab Natl Forestry & Grassland Adm Biodivers Co, Guiyang 550001, Peoples R China
[4] Sichuan Prov Acad Nat Resource Sci, Kiwifruit Breeding & Utilizat Key Lab Sichuan Prov, Chengdu 610015, Peoples R China
基金
中国国家自然科学基金;
关键词
Pectate lyase; Fragaria vesca; Expression pattern; Anther; Fruit ripening; AUXIN; ENZYMES;
D O I
10.1186/s12864-023-09533-9
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
BackgroundPectate lyase (PL, EC 4.2.2.2), as an endo-acting depolymerizing enzyme, cleaves & alpha;-1,4-glycosidic linkages in esterified pectin and involves a broad range of cell wall modifications. However, the knowledge concerning the genome-wide analysis of the PL gene family in Fragaria vesca has not been thoroughly elucidated.ResultsIn this study, sixteen PLs members in F. vesca were identified based on a genome-wide investigation. Substantial divergences existed among FvePLs in gene duplication, cis-acting elements, and tissue expression patterns. Four clusters were classified according to phylogenetic analysis. FvePL6, 8 and 13 in cluster II significantly contributed to the significant expansions during evolution by comparing orthologous PL genes from Malus domestica, Solanum lycopersicum, Arabidopsis thaliana, and Fragariaxananassa. The cis-acting elements implicated in the abscisic acid signaling pathway were abundant in the regions of FvePLs promoters. The RNA-seq data and in situ hybridization revealed that FvePL1, 4, and 7 exhibited maximum expression in fruits at twenty days after pollination, whereas FvePL8 and FvePL13 were preferentially and prominently expressed in mature anthers and pollens. Additionally, the co-expression networks displayed that FvePLs had tight correlations with transcription factors and genes implicated in plant development, abiotic/biotic stresses, ions/Ca2+, and hormones, suggesting the potential roles of FvePLs during strawberry development. Besides, histological observations suggested that FvePL1, 4 and 7 enhanced cell division and expansion of the cortex, thus negatively influencing fruit firmness. Finally, FvePL1-RNAi reduced leaf size, altered petal architectures, disrupted normal pollen development, and rendered partial male sterility.ConclusionThese results provide valuable information for characterizing the evolution, expansion, expression patterns and functional analysis, which help to understand the molecular mechanisms of the FvePLs in the development of strawberries.
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页数:16
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