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Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions

Previous studies suggested that Hd1 promoted heading under short-day conditions (SD) and delayed heading under long-day conditions (LD). However in this study, Hd1 was demonstrated to consistently promote heading date in Zhenshan 97 (ZS97) background by upregulating Ehd1, Hd3a and RFT1 expression un...

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Autores principales: Zhang, Zhanyi, Hu, Wei, Shen, Guojing, Liu, Haiyang, Hu, Yong, Zhou, Xiangchun, Liu, Touming, Xing, Yongzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511259/
https://www.ncbi.nlm.nih.gov/pubmed/28710485
http://dx.doi.org/10.1038/s41598-017-05873-1
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author Zhang, Zhanyi
Hu, Wei
Shen, Guojing
Liu, Haiyang
Hu, Yong
Zhou, Xiangchun
Liu, Touming
Xing, Yongzhong
author_facet Zhang, Zhanyi
Hu, Wei
Shen, Guojing
Liu, Haiyang
Hu, Yong
Zhou, Xiangchun
Liu, Touming
Xing, Yongzhong
author_sort Zhang, Zhanyi
collection PubMed
description Previous studies suggested that Hd1 promoted heading under short-day conditions (SD) and delayed heading under long-day conditions (LD). However in this study, Hd1 was demonstrated to consistently promote heading date in Zhenshan 97 (ZS97) background by upregulating Ehd1, Hd3a and RFT1 expression under both SD and LD. While the high photoperiod sensitivity of Hd1 was observed in Minghui 63 (MH63) background, with heading being suppressed in LD but promoted in SD. Comparative analysis of two sets of near isogenic lines of Hd1 in MH63 and ZS97 backgrounds indicated that the alternative functions of Hd1 in promoting or suppressing heading under LD are dependent on the previously cloned flowering repressor gene Ghd7. The interaction between proteins Ghd7 and Hd1 occurred through binding of the CCT domain of Ghd7 to the transcription-activating domain of Hd1, resulting in suppression of Ehd1 and florigen gene expression. The involvement of the transcription-activating domain of Hd1 in this protein-protein interaction probably blocked or weakened its transcriptional activity. These findings suggest that Hd1 alone essentially acts as a promoter of heading date, and the protein interaction between Ghd7 and Hd1 determines photoperiod sensitivity and integrated Hd1-mediated and Ehd1-mediated flowering pathways in rice.
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spelling pubmed-55112592017-07-17 Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions Zhang, Zhanyi Hu, Wei Shen, Guojing Liu, Haiyang Hu, Yong Zhou, Xiangchun Liu, Touming Xing, Yongzhong Sci Rep Article Previous studies suggested that Hd1 promoted heading under short-day conditions (SD) and delayed heading under long-day conditions (LD). However in this study, Hd1 was demonstrated to consistently promote heading date in Zhenshan 97 (ZS97) background by upregulating Ehd1, Hd3a and RFT1 expression under both SD and LD. While the high photoperiod sensitivity of Hd1 was observed in Minghui 63 (MH63) background, with heading being suppressed in LD but promoted in SD. Comparative analysis of two sets of near isogenic lines of Hd1 in MH63 and ZS97 backgrounds indicated that the alternative functions of Hd1 in promoting or suppressing heading under LD are dependent on the previously cloned flowering repressor gene Ghd7. The interaction between proteins Ghd7 and Hd1 occurred through binding of the CCT domain of Ghd7 to the transcription-activating domain of Hd1, resulting in suppression of Ehd1 and florigen gene expression. The involvement of the transcription-activating domain of Hd1 in this protein-protein interaction probably blocked or weakened its transcriptional activity. These findings suggest that Hd1 alone essentially acts as a promoter of heading date, and the protein interaction between Ghd7 and Hd1 determines photoperiod sensitivity and integrated Hd1-mediated and Ehd1-mediated flowering pathways in rice. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511259/ /pubmed/28710485 http://dx.doi.org/10.1038/s41598-017-05873-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhang, Zhanyi
Hu, Wei
Shen, Guojing
Liu, Haiyang
Hu, Yong
Zhou, Xiangchun
Liu, Touming
Xing, Yongzhong
Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title_full Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title_fullStr Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title_full_unstemmed Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title_short Alternative functions of Hd1 in repressing or promoting heading are determined by Ghd7 status under long-day conditions
title_sort alternative functions of hd1 in repressing or promoting heading are determined by ghd7 status under long-day conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511259/
https://www.ncbi.nlm.nih.gov/pubmed/28710485
http://dx.doi.org/10.1038/s41598-017-05873-1
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