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Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry

The critical role of auxin in strawberry fruit set and receptacle enlargement was demonstrated previously. While fertilization is known to trigger auxin biosynthesis, the specific tissue source of fertilization-induced auxin is not well understood. Here, the auxin reporter DR5ver2::GUS was introduce...

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Autores principales: Feng, Jia, Dai, Cheng, Luo, Huifeng, Han, Yafan, Liu, Zhongchi, Kang, Chunying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322568/
https://www.ncbi.nlm.nih.gov/pubmed/30371880
http://dx.doi.org/10.1093/jxb/ery384
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author Feng, Jia
Dai, Cheng
Luo, Huifeng
Han, Yafan
Liu, Zhongchi
Kang, Chunying
author_facet Feng, Jia
Dai, Cheng
Luo, Huifeng
Han, Yafan
Liu, Zhongchi
Kang, Chunying
author_sort Feng, Jia
collection PubMed
description The critical role of auxin in strawberry fruit set and receptacle enlargement was demonstrated previously. While fertilization is known to trigger auxin biosynthesis, the specific tissue source of fertilization-induced auxin is not well understood. Here, the auxin reporter DR5ver2::GUS was introduced into wild strawberry (Fragaria vesca) to reveal auxin distribution in the seed and fruit receptacle pre- and post-fertilization as well as in the root. In addition, the expression of TAR and YUCCA genes coding for enzymes catalysing the two-step auxin biosynthesis pathway was investigated using their respective promoters fused to the β-glucuronidase (GUS) reporter. Two FveTARs and four FveYUCs were shown to be expressed primarily in the endosperm and embryo inside the achenes as well as in root tips and lateral root primordia. Expression of these reporters in dissected tissues provided more detailed and precise spatial (cell and tissue) and temporal (pre- and post-fertilization) information on where auxin is synthesized and accumulates than previous studies in strawberry. Moreover, we generated CRISPR-mediated knock-out mutants of FveYUC10, the most abundant YUC in seeds; the mutants had a lower free auxin level in young fruit, but displayed no obvious morphological phenotypes. However, overexpression of FveYUC10 resulted in elongated hypocotyls in Arabidopsis caused by elevated auxin level. Overall, the study revealed auxin accumulation in the chalazal seed coat, embryo, receptacle vasculature, root tip, and lateral root primordia and highlighted the endosperm as the main auxin biosynthesis site for fruit set.
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spelling pubmed-63225682019-01-10 Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry Feng, Jia Dai, Cheng Luo, Huifeng Han, Yafan Liu, Zhongchi Kang, Chunying J Exp Bot Research Papers The critical role of auxin in strawberry fruit set and receptacle enlargement was demonstrated previously. While fertilization is known to trigger auxin biosynthesis, the specific tissue source of fertilization-induced auxin is not well understood. Here, the auxin reporter DR5ver2::GUS was introduced into wild strawberry (Fragaria vesca) to reveal auxin distribution in the seed and fruit receptacle pre- and post-fertilization as well as in the root. In addition, the expression of TAR and YUCCA genes coding for enzymes catalysing the two-step auxin biosynthesis pathway was investigated using their respective promoters fused to the β-glucuronidase (GUS) reporter. Two FveTARs and four FveYUCs were shown to be expressed primarily in the endosperm and embryo inside the achenes as well as in root tips and lateral root primordia. Expression of these reporters in dissected tissues provided more detailed and precise spatial (cell and tissue) and temporal (pre- and post-fertilization) information on where auxin is synthesized and accumulates than previous studies in strawberry. Moreover, we generated CRISPR-mediated knock-out mutants of FveYUC10, the most abundant YUC in seeds; the mutants had a lower free auxin level in young fruit, but displayed no obvious morphological phenotypes. However, overexpression of FveYUC10 resulted in elongated hypocotyls in Arabidopsis caused by elevated auxin level. Overall, the study revealed auxin accumulation in the chalazal seed coat, embryo, receptacle vasculature, root tip, and lateral root primordia and highlighted the endosperm as the main auxin biosynthesis site for fruit set. Oxford University Press 2019-01-15 2018-10-27 /pmc/articles/PMC6322568/ /pubmed/30371880 http://dx.doi.org/10.1093/jxb/ery384 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Feng, Jia
Dai, Cheng
Luo, Huifeng
Han, Yafan
Liu, Zhongchi
Kang, Chunying
Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title_full Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title_fullStr Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title_full_unstemmed Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title_short Reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
title_sort reporter gene expression reveals precise auxin synthesis sites during fruit and root development in wild strawberry
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322568/
https://www.ncbi.nlm.nih.gov/pubmed/30371880
http://dx.doi.org/10.1093/jxb/ery384
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