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Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)

Gene expression is regulated by transcription factors, which play many significant developmental processes. SQUAMOSA promoter-binding proteins (SBP) perform a variety of regulatory functions in leaf, flower, and fruit development, plant architecture, and sporogenesis. 16 SBP genes were identified in...

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Autores principales: Ali, Hina, Liu, Yanhui, Azam, Syed Muhammad, Rahman, Zia ur, Priyadarshani, S. V. G. N., Li, Weimin, Huang, Xinyu, Hu, Bingyan, Xiong, Junjie, Ali, Umair, Qin, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643045/
https://www.ncbi.nlm.nih.gov/pubmed/29104869
http://dx.doi.org/10.1155/2017/1032846
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author Ali, Hina
Liu, Yanhui
Azam, Syed Muhammad
Rahman, Zia ur
Priyadarshani, S. V. G. N.
Li, Weimin
Huang, Xinyu
Hu, Bingyan
Xiong, Junjie
Ali, Umair
Qin, Yuan
author_facet Ali, Hina
Liu, Yanhui
Azam, Syed Muhammad
Rahman, Zia ur
Priyadarshani, S. V. G. N.
Li, Weimin
Huang, Xinyu
Hu, Bingyan
Xiong, Junjie
Ali, Umair
Qin, Yuan
author_sort Ali, Hina
collection PubMed
description Gene expression is regulated by transcription factors, which play many significant developmental processes. SQUAMOSA promoter-binding proteins (SBP) perform a variety of regulatory functions in leaf, flower, and fruit development, plant architecture, and sporogenesis. 16 SBP genes were identified in pineapple and were divided into four groups on basis of phylogenetic analysis. Five paralogs in pineapple for SBP genes were identified with Ka/Ks ratio varied from 0.20 for AcSBP14 and AcSBP15 to 0.36 for AcSBP6 and AcSBP16, respectively. 16 SBP genes were located on 12 chromosomes out of 25 pineapple chromosomes with highly conserved protein sequence structures. The isoionic points of SBP ranged from 6.05 to 9.57, while molecular weight varied from 22.7 to 121.9 kD. Expression profiles of SBP genes revealed that AcSBP7 and AcSBP15 (leaf), AcSBP13, AcSBP12, AcSBP8, AcSBP16, AcSBP9, and AcSBP11 (sepal), AcSBP6, AcSBP4, and AcSBP10 (stamen), AcSBP14, AcSBP1, and AcSBP5 (fruit) while the rest of genes showed low expression in studied tissues. Four genes, that is, AcSBP11, AcSBP6, AcSBP4, and AcSBP12, were highly expressed at 4°C, while AcSBP16 were upregulated at 45°C. RNA-Seq was validated through qRT-PCR for some genes. Salt stress-induced expression of two genes, that is, AcSBP7 and AcSBP14, while in drought stress, AcSBP12 and AcSBP15 were highly expressed. Our study lays a foundation for further gene function and expression studies of SBP genes in pineapple.
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spelling pubmed-56430452017-11-05 Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.) Ali, Hina Liu, Yanhui Azam, Syed Muhammad Rahman, Zia ur Priyadarshani, S. V. G. N. Li, Weimin Huang, Xinyu Hu, Bingyan Xiong, Junjie Ali, Umair Qin, Yuan Int J Genomics Research Article Gene expression is regulated by transcription factors, which play many significant developmental processes. SQUAMOSA promoter-binding proteins (SBP) perform a variety of regulatory functions in leaf, flower, and fruit development, plant architecture, and sporogenesis. 16 SBP genes were identified in pineapple and were divided into four groups on basis of phylogenetic analysis. Five paralogs in pineapple for SBP genes were identified with Ka/Ks ratio varied from 0.20 for AcSBP14 and AcSBP15 to 0.36 for AcSBP6 and AcSBP16, respectively. 16 SBP genes were located on 12 chromosomes out of 25 pineapple chromosomes with highly conserved protein sequence structures. The isoionic points of SBP ranged from 6.05 to 9.57, while molecular weight varied from 22.7 to 121.9 kD. Expression profiles of SBP genes revealed that AcSBP7 and AcSBP15 (leaf), AcSBP13, AcSBP12, AcSBP8, AcSBP16, AcSBP9, and AcSBP11 (sepal), AcSBP6, AcSBP4, and AcSBP10 (stamen), AcSBP14, AcSBP1, and AcSBP5 (fruit) while the rest of genes showed low expression in studied tissues. Four genes, that is, AcSBP11, AcSBP6, AcSBP4, and AcSBP12, were highly expressed at 4°C, while AcSBP16 were upregulated at 45°C. RNA-Seq was validated through qRT-PCR for some genes. Salt stress-induced expression of two genes, that is, AcSBP7 and AcSBP14, while in drought stress, AcSBP12 and AcSBP15 were highly expressed. Our study lays a foundation for further gene function and expression studies of SBP genes in pineapple. Hindawi 2017 2017-09-29 /pmc/articles/PMC5643045/ /pubmed/29104869 http://dx.doi.org/10.1155/2017/1032846 Text en Copyright © 2017 Hina Ali et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ali, Hina
Liu, Yanhui
Azam, Syed Muhammad
Rahman, Zia ur
Priyadarshani, S. V. G. N.
Li, Weimin
Huang, Xinyu
Hu, Bingyan
Xiong, Junjie
Ali, Umair
Qin, Yuan
Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title_full Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title_fullStr Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title_full_unstemmed Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title_short Genomic Survey, Characterization, and Expression Profile Analysis of the SBP Genes in Pineapple (Ananas comosus L.)
title_sort genomic survey, characterization, and expression profile analysis of the sbp genes in pineapple (ananas comosus l.)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643045/
https://www.ncbi.nlm.nih.gov/pubmed/29104869
http://dx.doi.org/10.1155/2017/1032846
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