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Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak

Ginkgo biloba, a dioecious plant known as a living fossil, is an ancient gymnosperm that stands distinct from other gymnosperms and angiosperms. Ginkgo biloba var. epiphylla (G. biloba var. epiphylla), with ovules borne on the leaf blade, is an unusual germplasm derived from G. biloba. MicroRNAs (mi...

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Autores principales: Zhang, Qian, Li, Jihong, Sang, Yalin, Xing, Shiyan, Wu, Qikui, Liu, Xiaojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433266/
https://www.ncbi.nlm.nih.gov/pubmed/25978425
http://dx.doi.org/10.1371/journal.pone.0127184
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author Zhang, Qian
Li, Jihong
Sang, Yalin
Xing, Shiyan
Wu, Qikui
Liu, Xiaojing
author_facet Zhang, Qian
Li, Jihong
Sang, Yalin
Xing, Shiyan
Wu, Qikui
Liu, Xiaojing
author_sort Zhang, Qian
collection PubMed
description Ginkgo biloba, a dioecious plant known as a living fossil, is an ancient gymnosperm that stands distinct from other gymnosperms and angiosperms. Ginkgo biloba var. epiphylla (G. biloba var. epiphylla), with ovules borne on the leaf blade, is an unusual germplasm derived from G. biloba. MicroRNAs (miRNAs) are post-transcriptional gene regulators that play critical roles in diverse biological and metabolic processes. Currently, little is known about the miRNAs involved in the key stage of partly epiphyllous ovule germination in G. biloba var. epiphylla. Two small RNA libraries constructed from epiphyllous ovule leaves and normal leaves of G. biloba var. epiphylla were sequenced on an Illumina/Solexa platform. A total of 82 miRNA sequences belonging to 23 families and 53 putative novel miRNAs were identified in the two libraries. Differential expression analysis showed that 25 conserved and 21 novel miRNAs were differentially expressed between epiphyllous ovule leaves and normal leaves. The expression patterns of partially differentially expressed miRNAs and the transcript levels of their predicted target genes were validated by quantitative real time RT-PCR. All the expression profiles of the 21 selected miRNAs were similar to those detected by Solexa deep sequencing. Additionally, the transcript levels of almost all the putative target genes of 9 selected miRNAs were opposite to those of the corresponding miRNAs. The putative target genes of the differentially expressed miRNAs were annotated with Gene Ontology terms related to reproductive process, metabolic process and responding to stimulus. This work presents a broad range of small RNA transcriptome data obtained from epiphyllous ovule and normal leaves of G. biloba var. epiphylla, which may provide insights into the miRNA-mediated regulation in the epiphyllous ovule germination process.
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spelling pubmed-44332662015-05-27 Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak Zhang, Qian Li, Jihong Sang, Yalin Xing, Shiyan Wu, Qikui Liu, Xiaojing PLoS One Research Article Ginkgo biloba, a dioecious plant known as a living fossil, is an ancient gymnosperm that stands distinct from other gymnosperms and angiosperms. Ginkgo biloba var. epiphylla (G. biloba var. epiphylla), with ovules borne on the leaf blade, is an unusual germplasm derived from G. biloba. MicroRNAs (miRNAs) are post-transcriptional gene regulators that play critical roles in diverse biological and metabolic processes. Currently, little is known about the miRNAs involved in the key stage of partly epiphyllous ovule germination in G. biloba var. epiphylla. Two small RNA libraries constructed from epiphyllous ovule leaves and normal leaves of G. biloba var. epiphylla were sequenced on an Illumina/Solexa platform. A total of 82 miRNA sequences belonging to 23 families and 53 putative novel miRNAs were identified in the two libraries. Differential expression analysis showed that 25 conserved and 21 novel miRNAs were differentially expressed between epiphyllous ovule leaves and normal leaves. The expression patterns of partially differentially expressed miRNAs and the transcript levels of their predicted target genes were validated by quantitative real time RT-PCR. All the expression profiles of the 21 selected miRNAs were similar to those detected by Solexa deep sequencing. Additionally, the transcript levels of almost all the putative target genes of 9 selected miRNAs were opposite to those of the corresponding miRNAs. The putative target genes of the differentially expressed miRNAs were annotated with Gene Ontology terms related to reproductive process, metabolic process and responding to stimulus. This work presents a broad range of small RNA transcriptome data obtained from epiphyllous ovule and normal leaves of G. biloba var. epiphylla, which may provide insights into the miRNA-mediated regulation in the epiphyllous ovule germination process. Public Library of Science 2015-05-15 /pmc/articles/PMC4433266/ /pubmed/25978425 http://dx.doi.org/10.1371/journal.pone.0127184 Text en © 2015 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Qian
Li, Jihong
Sang, Yalin
Xing, Shiyan
Wu, Qikui
Liu, Xiaojing
Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title_full Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title_fullStr Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title_full_unstemmed Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title_short Identification and Characterization of MicroRNAs in Ginkgo biloba var. epiphylla Mak
title_sort identification and characterization of micrornas in ginkgo biloba var. epiphylla mak
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433266/
https://www.ncbi.nlm.nih.gov/pubmed/25978425
http://dx.doi.org/10.1371/journal.pone.0127184
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