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Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L

BACKGROUNDS: Pomegranate is an excellent tree species with nutritional, medicinal, ornamental and ecological values. Studies have confirmed that SPL factors play an important role in floral transition and flower development. RESULTS: Used bioinformatics methods, 15 SPL (SQUAMOSA promoter-binding pro...

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Autores principales: Li, Bianbian, Zhao, Yujie, Wang, Sha, Zhang, Xinhui, Wang, Yongwei, Shen, Yu, Yuan, Zhaohe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399725/
https://www.ncbi.nlm.nih.gov/pubmed/34454435
http://dx.doi.org/10.1186/s12870-021-03171-7
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author Li, Bianbian
Zhao, Yujie
Wang, Sha
Zhang, Xinhui
Wang, Yongwei
Shen, Yu
Yuan, Zhaohe
author_facet Li, Bianbian
Zhao, Yujie
Wang, Sha
Zhang, Xinhui
Wang, Yongwei
Shen, Yu
Yuan, Zhaohe
author_sort Li, Bianbian
collection PubMed
description BACKGROUNDS: Pomegranate is an excellent tree species with nutritional, medicinal, ornamental and ecological values. Studies have confirmed that SPL factors play an important role in floral transition and flower development. RESULTS: Used bioinformatics methods, 15 SPL (SQUAMOSA promoter-binding protein-like) genes were identified and analyzed from the ‘Taishanhong’ pomegranate (P. granatum L.) genome. Phylogenetic analysis showed that PgSPLs were divided into six subfamilies (G1 ~ G6). PgSPL promoter sequences contained multiple cis-acting elements associated with abiotic stress or hormonal response. Based on the transcriptome data, expression profiles of different tissues and different developmental stages showed that PgSPL genes had distinct temporal and spatial expression characteristics. The expression analysis of miR156 in small RNA sequencing results showed that miR156 negatively regulated the expression of target genes. qRT-PCR analysis showed that the expression levels of PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 in leaves were significantly higher than those in buds and stems (p < 0.05). The expression levels of PgSPL5, PgSPL12 and PgSPL13 in flower buds were significantly higher than that in leaves and stems (p < 0.05). The full-length of coding sequence of PgSPL5 and PgSPL13 were obtained by homologous cloning technology. The full length of PgSPL5 is 1020 bp, and PgSPL13 is 489 bp, which encodes 339 and 162 amino acids, respectively. Further investigation revealed that PgSPL5 and PgSPL13 proteins were located in the nucleus. Exogenous plant growth regulator induction experiments showed that PgSPL5 was up-regulated in leaves and stems. PgSPL13 was up-regulated in leaves and down-regulated in stems. When sprayed with 6-BA, IBA and PP333 respectively, PgSPL5 and PgSPL13 were up-regulated most significantly at P2 (bud vertical diameter was 5.1 ~ 12.0 mm) stage of bisexual and functional male flowers. CONCLUSIONS: Our findings suggested that PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 played roles in leaves development of pomegranate. PgSPL5, PgSPL12 and PgSPL13 played roles in pomegranate flower development. PgSPL5 and PgSPL13 were involved in the response process of different plant hormone signal transduction in pomegranate development. This study provided a robust basis for further functional analyses of SPL genes in pomegranate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03171-7.
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spelling pubmed-83997252021-08-30 Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L Li, Bianbian Zhao, Yujie Wang, Sha Zhang, Xinhui Wang, Yongwei Shen, Yu Yuan, Zhaohe BMC Plant Biol Research BACKGROUNDS: Pomegranate is an excellent tree species with nutritional, medicinal, ornamental and ecological values. Studies have confirmed that SPL factors play an important role in floral transition and flower development. RESULTS: Used bioinformatics methods, 15 SPL (SQUAMOSA promoter-binding protein-like) genes were identified and analyzed from the ‘Taishanhong’ pomegranate (P. granatum L.) genome. Phylogenetic analysis showed that PgSPLs were divided into six subfamilies (G1 ~ G6). PgSPL promoter sequences contained multiple cis-acting elements associated with abiotic stress or hormonal response. Based on the transcriptome data, expression profiles of different tissues and different developmental stages showed that PgSPL genes had distinct temporal and spatial expression characteristics. The expression analysis of miR156 in small RNA sequencing results showed that miR156 negatively regulated the expression of target genes. qRT-PCR analysis showed that the expression levels of PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 in leaves were significantly higher than those in buds and stems (p < 0.05). The expression levels of PgSPL5, PgSPL12 and PgSPL13 in flower buds were significantly higher than that in leaves and stems (p < 0.05). The full-length of coding sequence of PgSPL5 and PgSPL13 were obtained by homologous cloning technology. The full length of PgSPL5 is 1020 bp, and PgSPL13 is 489 bp, which encodes 339 and 162 amino acids, respectively. Further investigation revealed that PgSPL5 and PgSPL13 proteins were located in the nucleus. Exogenous plant growth regulator induction experiments showed that PgSPL5 was up-regulated in leaves and stems. PgSPL13 was up-regulated in leaves and down-regulated in stems. When sprayed with 6-BA, IBA and PP333 respectively, PgSPL5 and PgSPL13 were up-regulated most significantly at P2 (bud vertical diameter was 5.1 ~ 12.0 mm) stage of bisexual and functional male flowers. CONCLUSIONS: Our findings suggested that PgSPL2, PgSPL3, PgSPL6, PgSPL11 and PgSPL14 played roles in leaves development of pomegranate. PgSPL5, PgSPL12 and PgSPL13 played roles in pomegranate flower development. PgSPL5 and PgSPL13 were involved in the response process of different plant hormone signal transduction in pomegranate development. This study provided a robust basis for further functional analyses of SPL genes in pomegranate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03171-7. BioMed Central 2021-08-28 /pmc/articles/PMC8399725/ /pubmed/34454435 http://dx.doi.org/10.1186/s12870-021-03171-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Li, Bianbian
Zhao, Yujie
Wang, Sha
Zhang, Xinhui
Wang, Yongwei
Shen, Yu
Yuan, Zhaohe
Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title_full Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title_fullStr Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title_full_unstemmed Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title_short Genome-wide identification, gene cloning, subcellular location and expression analysis of SPL gene family in P. granatum L
title_sort genome-wide identification, gene cloning, subcellular location and expression analysis of spl gene family in p. granatum l
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8399725/
https://www.ncbi.nlm.nih.gov/pubmed/34454435
http://dx.doi.org/10.1186/s12870-021-03171-7
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