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Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa
Long non-coding RNAs (lncRNAs) function in various biological processes. However, their roles in secondary growth of plants remain poorly understood. Here, 15,691 lncRNAs were identified from vascular cambium, developing xylem, and mature xylem of Populus tomentosa with high and low biomass using RN...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737087/ https://www.ncbi.nlm.nih.gov/pubmed/28453813 http://dx.doi.org/10.1093/dnares/dsx018 |
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author | Zhou, Daling Du, Qingzhang Chen, Jinhui Wang, Qingshi Zhang, Deqiang |
author_facet | Zhou, Daling Du, Qingzhang Chen, Jinhui Wang, Qingshi Zhang, Deqiang |
author_sort | Zhou, Daling |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) function in various biological processes. However, their roles in secondary growth of plants remain poorly understood. Here, 15,691 lncRNAs were identified from vascular cambium, developing xylem, and mature xylem of Populus tomentosa with high and low biomass using RNA-seq, including 1,994 lncRNAs that were differentially expressed (DE) among the six libraries. 3,569 cis-regulated and 3,297 trans-regulated protein-coding genes were predicted as potential target genes (PTGs) of the DE lncRNAs to participate in biological regulation. Then, 476 and 28 lncRNAs were identified as putative targets and endogenous target mimics (eTMs) of Populus known microRNAs (miRNAs), respectively. Genome re-sequencing of 435 individuals from a natural population of P. tomentosa found 34,015 single nucleotide polymorphisms (SNPs) within 178 lncRNA loci and 522 PTGs. Single-SNP associations analysis detected 2,993 associations with 10 growth and wood-property traits under additive and dominance model. Epistasis analysis identified 17,656 epistatic SNP pairs, providing evidence for potential regulatory interactions between lncRNAs and their PTGs. Furthermore, a reconstructed epistatic network, representing interactions of 8 lncRNAs and 15 PTGs, might enrich regulation roles of genes in the phenylpropanoid pathway. These findings may enhance our understanding of non-coding genes in plants. |
format | Online Article Text |
id | pubmed-5737087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57370872018-01-08 Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa Zhou, Daling Du, Qingzhang Chen, Jinhui Wang, Qingshi Zhang, Deqiang DNA Res Full Papers Long non-coding RNAs (lncRNAs) function in various biological processes. However, their roles in secondary growth of plants remain poorly understood. Here, 15,691 lncRNAs were identified from vascular cambium, developing xylem, and mature xylem of Populus tomentosa with high and low biomass using RNA-seq, including 1,994 lncRNAs that were differentially expressed (DE) among the six libraries. 3,569 cis-regulated and 3,297 trans-regulated protein-coding genes were predicted as potential target genes (PTGs) of the DE lncRNAs to participate in biological regulation. Then, 476 and 28 lncRNAs were identified as putative targets and endogenous target mimics (eTMs) of Populus known microRNAs (miRNAs), respectively. Genome re-sequencing of 435 individuals from a natural population of P. tomentosa found 34,015 single nucleotide polymorphisms (SNPs) within 178 lncRNA loci and 522 PTGs. Single-SNP associations analysis detected 2,993 associations with 10 growth and wood-property traits under additive and dominance model. Epistasis analysis identified 17,656 epistatic SNP pairs, providing evidence for potential regulatory interactions between lncRNAs and their PTGs. Furthermore, a reconstructed epistatic network, representing interactions of 8 lncRNAs and 15 PTGs, might enrich regulation roles of genes in the phenylpropanoid pathway. These findings may enhance our understanding of non-coding genes in plants. Oxford University Press 2017-10 2017-04-26 /pmc/articles/PMC5737087/ /pubmed/28453813 http://dx.doi.org/10.1093/dnares/dsx018 Text en © The Author 2017. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Full Papers Zhou, Daling Du, Qingzhang Chen, Jinhui Wang, Qingshi Zhang, Deqiang Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title | Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title_full | Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title_fullStr | Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title_full_unstemmed | Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title_short | Identification and allelic dissection uncover roles of lncRNAs in secondary growth of Populus tomentosa |
title_sort | identification and allelic dissection uncover roles of lncrnas in secondary growth of populus tomentosa |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737087/ https://www.ncbi.nlm.nih.gov/pubmed/28453813 http://dx.doi.org/10.1093/dnares/dsx018 |
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