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Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca
BACKGROUND: Pectate lyase (PL, EC 4.2.2.2), as an endo-acting depolymerizing enzyme, cleaves α-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 no...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401794/ https://www.ncbi.nlm.nih.gov/pubmed/37537572 http://dx.doi.org/10.1186/s12864-023-09533-9 |
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author | Huang, Xiaolong Sun, Guilian Wu, Zongmin Jiang, Yu Li, Qiaohong Yi, Yin Yan, Huiqing |
author_facet | Huang, Xiaolong Sun, Guilian Wu, Zongmin Jiang, Yu Li, Qiaohong Yi, Yin Yan, Huiqing |
author_sort | Huang, Xiaolong |
collection | PubMed |
description | BACKGROUND: Pectate lyase (PL, EC 4.2.2.2), as an endo-acting depolymerizing enzyme, cleaves α-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. RESULTS: In 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 Fragaria×ananassa. 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/Ca(2+), 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. CONCLUSION: These 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09533-9. |
format | Online Article Text |
id | pubmed-10401794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104017942023-08-05 Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca Huang, Xiaolong Sun, Guilian Wu, Zongmin Jiang, Yu Li, Qiaohong Yi, Yin Yan, Huiqing BMC Genomics Research BACKGROUND: Pectate lyase (PL, EC 4.2.2.2), as an endo-acting depolymerizing enzyme, cleaves α-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. RESULTS: In 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 Fragaria×ananassa. 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/Ca(2+), 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. CONCLUSION: These 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09533-9. BioMed Central 2023-08-03 /pmc/articles/PMC10401794/ /pubmed/37537572 http://dx.doi.org/10.1186/s12864-023-09533-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Huang, Xiaolong Sun, Guilian Wu, Zongmin Jiang, Yu Li, Qiaohong Yi, Yin Yan, Huiqing Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title | Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title_full | Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title_fullStr | Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title_full_unstemmed | Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title_short | Genome-wide identification and expression analyses of the pectate lyase (PL) gene family in Fragaria vesca |
title_sort | genome-wide identification and expression analyses of the pectate lyase (pl) gene family in fragaria vesca |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401794/ https://www.ncbi.nlm.nih.gov/pubmed/37537572 http://dx.doi.org/10.1186/s12864-023-09533-9 |
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