Cargando…

Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)

PISTILLATA (PI)-like genes are crucial regulators of flowering in angiosperms. A homologue of PI, designated as AcPI (Genbank accession number HQ717796), was isolated from pineapple cultivar Comte de Paris by reverse transcriptase polymerase chain reaction (RT-PCR) and rapid amplification of cDNA en...

Descripción completa

Detalles Bibliográficos
Autores principales: Lv, Ling-Ling, Duan, Jun, Xie, Jiang-Hui, Liu, Yu-Ge, Wei, Chang-Bin, Liu, Sheng-Hui, Zhang, Jian-Xia, Sun, Guang-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269737/
https://www.ncbi.nlm.nih.gov/pubmed/22312303
http://dx.doi.org/10.3390/ijms13011039
_version_ 1782222504529494016
author Lv, Ling-Ling
Duan, Jun
Xie, Jiang-Hui
Liu, Yu-Ge
Wei, Chang-Bin
Liu, Sheng-Hui
Zhang, Jian-Xia
Sun, Guang-Ming
author_facet Lv, Ling-Ling
Duan, Jun
Xie, Jiang-Hui
Liu, Yu-Ge
Wei, Chang-Bin
Liu, Sheng-Hui
Zhang, Jian-Xia
Sun, Guang-Ming
author_sort Lv, Ling-Ling
collection PubMed
description PISTILLATA (PI)-like genes are crucial regulators of flowering in angiosperms. A homologue of PI, designated as AcPI (Genbank accession number HQ717796), was isolated from pineapple cultivar Comte de Paris by reverse transcriptase polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE). The cDNA sequence of AcPI is 907 bp in length and contains an open reading frame of 594 bp, which encodes a protein of 197 amino acids. The molecular weight was 2.29 kDa and the isoelectric point was 9.28. The alignment showed that AcPI had a high identity with CsPIC2 (78.6%), AoPI (77.4%), OrcPI (75.7%) and HPI2 (72.4%). Quantitative real-time polymerase chain reaction (qRT-PCR) analyses in different tissues showed that the expression pattern of AcPI was different from the B-class genes in eudicots. AcPI was expressed in all the tissues investigated. The expression level was very low in fruit stems, bracts, leaves and sepals, high in petals and carpels, and moderate in apical meristems, flesh and stamens. The qRT-PCR analyses in different stages indicated that the expression of AcPI reached the highest level at 40 days after flower inducement, when the multiple fruit and floral organs were forming. It proved the important role of AcPI in floral organs and fruit development. The 35S::AcPI transgenic Arabidopsis plants flowered earlier and had more inflorescences or branches than wild type plants.
format Online
Article
Text
id pubmed-3269737
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Molecular Diversity Preservation International (MDPI)
record_format MEDLINE/PubMed
spelling pubmed-32697372012-02-06 Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr) Lv, Ling-Ling Duan, Jun Xie, Jiang-Hui Liu, Yu-Ge Wei, Chang-Bin Liu, Sheng-Hui Zhang, Jian-Xia Sun, Guang-Ming Int J Mol Sci Article PISTILLATA (PI)-like genes are crucial regulators of flowering in angiosperms. A homologue of PI, designated as AcPI (Genbank accession number HQ717796), was isolated from pineapple cultivar Comte de Paris by reverse transcriptase polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE). The cDNA sequence of AcPI is 907 bp in length and contains an open reading frame of 594 bp, which encodes a protein of 197 amino acids. The molecular weight was 2.29 kDa and the isoelectric point was 9.28. The alignment showed that AcPI had a high identity with CsPIC2 (78.6%), AoPI (77.4%), OrcPI (75.7%) and HPI2 (72.4%). Quantitative real-time polymerase chain reaction (qRT-PCR) analyses in different tissues showed that the expression pattern of AcPI was different from the B-class genes in eudicots. AcPI was expressed in all the tissues investigated. The expression level was very low in fruit stems, bracts, leaves and sepals, high in petals and carpels, and moderate in apical meristems, flesh and stamens. The qRT-PCR analyses in different stages indicated that the expression of AcPI reached the highest level at 40 days after flower inducement, when the multiple fruit and floral organs were forming. It proved the important role of AcPI in floral organs and fruit development. The 35S::AcPI transgenic Arabidopsis plants flowered earlier and had more inflorescences or branches than wild type plants. Molecular Diversity Preservation International (MDPI) 2012-01-19 /pmc/articles/PMC3269737/ /pubmed/22312303 http://dx.doi.org/10.3390/ijms13011039 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Lv, Ling-Ling
Duan, Jun
Xie, Jiang-Hui
Liu, Yu-Ge
Wei, Chang-Bin
Liu, Sheng-Hui
Zhang, Jian-Xia
Sun, Guang-Ming
Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title_full Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title_fullStr Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title_full_unstemmed Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title_short Cloning and Expression Analysis of a PISTILLATA Homologous Gene from Pineapple (Ananas comosus L. Merr)
title_sort cloning and expression analysis of a pistillata homologous gene from pineapple (ananas comosus l. merr)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269737/
https://www.ncbi.nlm.nih.gov/pubmed/22312303
http://dx.doi.org/10.3390/ijms13011039
work_keys_str_mv AT lvlingling cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT duanjun cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT xiejianghui cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT liuyuge cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT weichangbin cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT liushenghui cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT zhangjianxia cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr
AT sunguangming cloningandexpressionanalysisofapistillatahomologousgenefrompineappleananascomosuslmerr