Cargando…

PbrmiR397a regulates lignification during stone cell development in pear fruit

Lignified stone cells substantially reduce fruit quality. Therefore, it is desirable to inhibit stone cell development using genetic technologies. However, the molecular mechanisms regulating lignification are poorly understood in fruit stone cells. In this study, we have shown that microRNA (miR) m...

Descripción completa

Detalles Bibliográficos
Autores principales: Xue, Cheng, Yao, Jia‐Long, Qin, Meng‐Fan, Zhang, Ming‐Yue, Allan, Andrew C., Wang, De‐Fu, Wu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330545/
https://www.ncbi.nlm.nih.gov/pubmed/29754465
http://dx.doi.org/10.1111/pbi.12950
_version_ 1783386998971564032
author Xue, Cheng
Yao, Jia‐Long
Qin, Meng‐Fan
Zhang, Ming‐Yue
Allan, Andrew C.
Wang, De‐Fu
Wu, Jun
author_facet Xue, Cheng
Yao, Jia‐Long
Qin, Meng‐Fan
Zhang, Ming‐Yue
Allan, Andrew C.
Wang, De‐Fu
Wu, Jun
author_sort Xue, Cheng
collection PubMed
description Lignified stone cells substantially reduce fruit quality. Therefore, it is desirable to inhibit stone cell development using genetic technologies. However, the molecular mechanisms regulating lignification are poorly understood in fruit stone cells. In this study, we have shown that microRNA (miR) miR397a regulates fruit cell lignification by inhibiting laccase (LAC) genes that encode key lignin biosynthesis enzymes. Transient overexpression of PbrmiR397a, which is the miR397a of Chinese pear (Pyrus bretschneideri), and simultaneous silencing of three LAC genes reduced the lignin content and stone cell number in pear fruit. A single nucleotide polymorphism (SNP) identified in the promoter of the PbrmiR397a gene was found to associate with low levels of fruit lignin, after analysis of the genome sequences of sixty pear varieties. This SNP created a TCA element that responded to salicylic acid to induce gene expression as confirmed using a cell‐based assay system. Furthermore, stable overexpression of PbrmiR397a in transgenic tobacco plants reduced the expression of target LAC genes and decreased the content of lignin but did not change the ratio of syringyl‐ and guaiacyl‐lignin monomers. Consistent with reduction in lignin content, the transgenic plants showed fewer numbers of vessel elements and thinner secondary walls in the remaining elements compared to wild‐type control plants. This study has advanced our understanding of the regulation of lignin biosynthesis and provided useful molecular genetic information for improving pear fruit quality.
format Online
Article
Text
id pubmed-6330545
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-63305452019-01-17 PbrmiR397a regulates lignification during stone cell development in pear fruit Xue, Cheng Yao, Jia‐Long Qin, Meng‐Fan Zhang, Ming‐Yue Allan, Andrew C. Wang, De‐Fu Wu, Jun Plant Biotechnol J Research Articles Lignified stone cells substantially reduce fruit quality. Therefore, it is desirable to inhibit stone cell development using genetic technologies. However, the molecular mechanisms regulating lignification are poorly understood in fruit stone cells. In this study, we have shown that microRNA (miR) miR397a regulates fruit cell lignification by inhibiting laccase (LAC) genes that encode key lignin biosynthesis enzymes. Transient overexpression of PbrmiR397a, which is the miR397a of Chinese pear (Pyrus bretschneideri), and simultaneous silencing of three LAC genes reduced the lignin content and stone cell number in pear fruit. A single nucleotide polymorphism (SNP) identified in the promoter of the PbrmiR397a gene was found to associate with low levels of fruit lignin, after analysis of the genome sequences of sixty pear varieties. This SNP created a TCA element that responded to salicylic acid to induce gene expression as confirmed using a cell‐based assay system. Furthermore, stable overexpression of PbrmiR397a in transgenic tobacco plants reduced the expression of target LAC genes and decreased the content of lignin but did not change the ratio of syringyl‐ and guaiacyl‐lignin monomers. Consistent with reduction in lignin content, the transgenic plants showed fewer numbers of vessel elements and thinner secondary walls in the remaining elements compared to wild‐type control plants. This study has advanced our understanding of the regulation of lignin biosynthesis and provided useful molecular genetic information for improving pear fruit quality. John Wiley and Sons Inc. 2018-06-21 2019-01 /pmc/articles/PMC6330545/ /pubmed/29754465 http://dx.doi.org/10.1111/pbi.12950 Text en © 2018 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Xue, Cheng
Yao, Jia‐Long
Qin, Meng‐Fan
Zhang, Ming‐Yue
Allan, Andrew C.
Wang, De‐Fu
Wu, Jun
PbrmiR397a regulates lignification during stone cell development in pear fruit
title PbrmiR397a regulates lignification during stone cell development in pear fruit
title_full PbrmiR397a regulates lignification during stone cell development in pear fruit
title_fullStr PbrmiR397a regulates lignification during stone cell development in pear fruit
title_full_unstemmed PbrmiR397a regulates lignification during stone cell development in pear fruit
title_short PbrmiR397a regulates lignification during stone cell development in pear fruit
title_sort pbrmir397a regulates lignification during stone cell development in pear fruit
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330545/
https://www.ncbi.nlm.nih.gov/pubmed/29754465
http://dx.doi.org/10.1111/pbi.12950
work_keys_str_mv AT xuecheng pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT yaojialong pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT qinmengfan pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT zhangmingyue pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT allanandrewc pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT wangdefu pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit
AT wujun pbrmir397aregulateslignificationduringstonecelldevelopmentinpearfruit