Cargando…

MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach

Bud dormancy is crucial for winter survival and is characterized by the inability of the bud meristem to respond to growth-promotive signals before the chilling requirement (CR) is met. However, our understanding of the genetic mechanism regulating CR and bud dormancy remains limited. This study ide...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ya-Lin, Li, Yong, Cao, Ke, Yao, Jia-Long, Bie, Hang-Ling, Khan, Irshad Ahmad, Fang, Wei-Chao, Chen, Chang-Wen, Wang, Xin-Wei, Wu, Jin-Long, Guo, Wen-Wu, Wang, Li-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469376/
https://www.ncbi.nlm.nih.gov/pubmed/37217835
http://dx.doi.org/10.1093/plphys/kiad291
_version_ 1785099426002370560
author Zhao, Ya-Lin
Li, Yong
Cao, Ke
Yao, Jia-Long
Bie, Hang-Ling
Khan, Irshad Ahmad
Fang, Wei-Chao
Chen, Chang-Wen
Wang, Xin-Wei
Wu, Jin-Long
Guo, Wen-Wu
Wang, Li-Rong
author_facet Zhao, Ya-Lin
Li, Yong
Cao, Ke
Yao, Jia-Long
Bie, Hang-Ling
Khan, Irshad Ahmad
Fang, Wei-Chao
Chen, Chang-Wen
Wang, Xin-Wei
Wu, Jin-Long
Guo, Wen-Wu
Wang, Li-Rong
author_sort Zhao, Ya-Lin
collection PubMed
description Bud dormancy is crucial for winter survival and is characterized by the inability of the bud meristem to respond to growth-promotive signals before the chilling requirement (CR) is met. However, our understanding of the genetic mechanism regulating CR and bud dormancy remains limited. This study identified PpDAM6 (DORMANCY-ASSOCIATED MADS-box) as a key gene for CR using a genome-wide association study analysis based on structural variations in 345 peach (Prunus persica (L.) Batsch) accessions. The function of PpDAM6 in CR regulation was demonstrated by transiently silencing the gene in peach buds and stably overexpressing the gene in transgenic apple (Malus × domestica) plants. The results showed an evolutionarily conserved function of PpDAM6 in regulating bud dormancy release, followed by vegetative growth and flowering, in peach and apple. The 30-bp deletion in the PpDAM6 promoter was substantially associated with reducing PpDAM6 expression in low-CR accessions. A PCR marker based on the 30-bp indel was developed to distinguish peach plants with non-low and low CR. Modification of the H3K27me3 marker at the PpDAM6 locus showed no apparent change across the dormancy process in low- and non-low- CR cultivars. Additionally, H3K27me3 modification occurred earlier in low-CR cultivars on a genome-wide scale. PpDAM6 could mediate cell–cell communication by inducing the expression of the downstream genes PpNCED1 (9-cis-epoxycarotenoid dioxygenase 1), encoding a key enzyme for ABA biosynthesis, and CALS (CALLOSE SYNTHASE), encoding callose synthase. We shed light on a gene regulatory network formed by PpDAM6-containing complexes that mediate CR underlying dormancy and bud break in peach. A better understanding of the genetic basis for natural variations of CR can help breeders develop cultivars with different CR for growing in different geographical regions.
format Online
Article
Text
id pubmed-10469376
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-104693762023-09-01 MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach Zhao, Ya-Lin Li, Yong Cao, Ke Yao, Jia-Long Bie, Hang-Ling Khan, Irshad Ahmad Fang, Wei-Chao Chen, Chang-Wen Wang, Xin-Wei Wu, Jin-Long Guo, Wen-Wu Wang, Li-Rong Plant Physiol Research Article Bud dormancy is crucial for winter survival and is characterized by the inability of the bud meristem to respond to growth-promotive signals before the chilling requirement (CR) is met. However, our understanding of the genetic mechanism regulating CR and bud dormancy remains limited. This study identified PpDAM6 (DORMANCY-ASSOCIATED MADS-box) as a key gene for CR using a genome-wide association study analysis based on structural variations in 345 peach (Prunus persica (L.) Batsch) accessions. The function of PpDAM6 in CR regulation was demonstrated by transiently silencing the gene in peach buds and stably overexpressing the gene in transgenic apple (Malus × domestica) plants. The results showed an evolutionarily conserved function of PpDAM6 in regulating bud dormancy release, followed by vegetative growth and flowering, in peach and apple. The 30-bp deletion in the PpDAM6 promoter was substantially associated with reducing PpDAM6 expression in low-CR accessions. A PCR marker based on the 30-bp indel was developed to distinguish peach plants with non-low and low CR. Modification of the H3K27me3 marker at the PpDAM6 locus showed no apparent change across the dormancy process in low- and non-low- CR cultivars. Additionally, H3K27me3 modification occurred earlier in low-CR cultivars on a genome-wide scale. PpDAM6 could mediate cell–cell communication by inducing the expression of the downstream genes PpNCED1 (9-cis-epoxycarotenoid dioxygenase 1), encoding a key enzyme for ABA biosynthesis, and CALS (CALLOSE SYNTHASE), encoding callose synthase. We shed light on a gene regulatory network formed by PpDAM6-containing complexes that mediate CR underlying dormancy and bud break in peach. A better understanding of the genetic basis for natural variations of CR can help breeders develop cultivars with different CR for growing in different geographical regions. Oxford University Press 2023-05-22 /pmc/articles/PMC10469376/ /pubmed/37217835 http://dx.doi.org/10.1093/plphys/kiad291 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Zhao, Ya-Lin
Li, Yong
Cao, Ke
Yao, Jia-Long
Bie, Hang-Ling
Khan, Irshad Ahmad
Fang, Wei-Chao
Chen, Chang-Wen
Wang, Xin-Wei
Wu, Jin-Long
Guo, Wen-Wu
Wang, Li-Rong
MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title_full MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title_fullStr MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title_full_unstemmed MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title_short MADS-box protein PpDAM6 regulates chilling requirement-mediated dormancy and bud break in peach
title_sort mads-box protein ppdam6 regulates chilling requirement-mediated dormancy and bud break in peach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469376/
https://www.ncbi.nlm.nih.gov/pubmed/37217835
http://dx.doi.org/10.1093/plphys/kiad291
work_keys_str_mv AT zhaoyalin madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT liyong madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT caoke madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT yaojialong madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT biehangling madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT khanirshadahmad madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT fangweichao madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT chenchangwen madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT wangxinwei madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT wujinlong madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT guowenwu madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach
AT wanglirong madsboxproteinppdam6regulateschillingrequirementmediateddormancyandbudbreakinpeach