» Articles » PMID: 33518715

KSN Heterozygosity is Associated with Continuous Flowering of Rosa Rugosa Purple Branch

Overview
Journal Hortic Res
Date 2021 Feb 1
PMID 33518715
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Rose (Rosa spp.) plants flower via two contrasting methods: once flowering (OF) and continuous flowering (CF). Purple branch is a rare continuously flowering variety of Rosa rugosa that is extensively cultivated in China. However, the genetic basis of its CF behavior is unknown. We demonstrated that Purple branch is heterozygous for the TFL1 homolog KSN. One KSN allele with a 9 kb Copia insertion was found to be identical to that from continuously flowering Rosa chinensis Old blush. The other allele was found to be a functional wild-type allele. The overall expression of KSN was closely linked to the floral transition, and it was significantly repressed in continuously flowering Purple branch compared with OF Plena. The promoter region of the normal KSN allele was hypermethylated, and histone methylation at H3H4, H3K9, and H3K27 of the KSN gene locus was modified in continuously flowering Purple branch. Silencing of the DNA methyltransferase genes MET1 and CMT3 and the histone methyltransferase gene SUVR5 in Purple branch led to enhanced KSN expression, but silencing of the histone demethylase gene JMJ12 suppressed KSN expression. Therefore, the CF habit of Purple branch may be due to reduced expression of KSN caused by the halved dose and may be associated with epigenetic modifications together with retrotransposon insertions along the chromosome. Our study revealed a novel mechanism underlying the CF behavior of rose plants.

Citing Articles

Molecular cloning and characterization of farnesyl diphosphate synthase from Thunb associated with salinity stress.

Wei G, Chen Y, Wang J, Feng L PeerJ. 2024; 12:e16929.

PMID: 38435988 PMC: 10909355. DOI: 10.7717/peerj.16929.


Gene-flow investigation between garden and wild roses planted in close distance.

Asagoshi Y, Hitomi E, Nakamura N, Takeda S Plant Biotechnol (Tokyo). 2024; 40(4):283-288.

PMID: 38434113 PMC: 10905366. DOI: 10.5511/plantbiotechnology.23.0708a.


Identification of flowering genes in Camellia perpetua by comparative transcriptome analysis.

Yu J, Cui J, Huang H, Cen D, Liu F, Xu Z Funct Integr Genomics. 2023; 24(1):2.

PMID: 38066213 DOI: 10.1007/s10142-023-01267-x.


Rose long noncoding RNA lncWD83 promotes flowering by modulating ubiquitination of the floral repressor RcMYC2L.

Yeqing C, Jun L, Weinan W, Chunguo F, Guozhen Y, Jingjing S Plant Physiol. 2023; 193(4):2573-2591.

PMID: 37723122 PMC: 10663112. DOI: 10.1093/plphys/kiad502.


Advances in DNA methylation and demethylation in medicinal plants: a review.

Zang Y, Xie L, Su J, Luo Z, Jia X, Ma X Mol Biol Rep. 2023; 50(9):7783-7796.

PMID: 37480509 DOI: 10.1007/s11033-023-08618-8.


References
1.
Lu J, Bai M, Ren H, Liu J, Wang C . An efficient transient expression system for gene function analysis in rose. Plant Methods. 2018; 13:116. PMC: 5740963. DOI: 10.1186/s13007-017-0268-1. View

2.
Jenuwein T, Allis C . Translating the histone code. Science. 2001; 293(5532):1074-80. DOI: 10.1126/science.1063127. View

3.
Bradley D, Ratcliffe O, Vincent C, Carpenter R, Coen E . Inflorescence commitment and architecture in Arabidopsis. Science. 1997; 275(5296):80-3. DOI: 10.1126/science.275.5296.80. View

4.
Thorstensen T, Grini P, Aalen R . SET domain proteins in plant development. Biochim Biophys Acta. 2011; 1809(8):407-20. DOI: 10.1016/j.bbagrm.2011.05.008. View

5.
Lippman Z, Gendrel A, Black M, Vaughn M, Dedhia N, McCombie W . Role of transposable elements in heterochromatin and epigenetic control. Nature. 2004; 430(6998):471-6. DOI: 10.1038/nature02651. View