- Award ID(s):
- 1755224
- PAR ID:
- 10471668
- Editor(s):
- Köhler, C
- Publisher / Repository:
- PLOS Genetics
- Date Published:
- Journal Name:
- PLOS Genetics
- Volume:
- 19
- Issue:
- 9
- ISSN:
- 1553-7404
- Page Range / eLocation ID:
- e1010955
- Subject(s) / Keyword(s):
- PHYTOCHROME C photoperiod flowering PHOTOPERIOD1 EARLY FLOWERING 3 Brachypodium distachyon
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
The proper timing of flowering, which is key to maximize reproductive success and yield, relies in many plant species on the coordination between environmental cues and endogenous developmental programs. The perception of changes in day length is one of the most reliable cues of seasonal change, and this involves the interplay between the sensing of light signals and the circadian clock. Here, we describe a Brachypodium distachyon mutant allele of the evening complex protein EARLY FLOWERING 3 (ELF3). We show that the elf3 mutant flowers more rapidly than wild type plants in short days as well as under longer photoperiods but, in very long (20 h) days, flowering is equally rapid in elf3 and wild type. Furthermore, flowering in the elf3 mutant is still sensitive to vernalization, but not to ambient temperature changes. Molecular analyses revealed that the expression of a short-day marker gene is suppressed in elf3 grown in short days, and the expression patterns of clock genes and flowering time regulators are altered. We also explored the mechanisms of photoperiodic perception in temperate grasses by exposing B. distachyon plants grown under a 12 h photoperiod to a daily night break consisting of a mixture of red and far-red light. We showed that 2 h breaks are sufficient to accelerate flowering in B. distachyon under non-inductive photoperiods and that this acceleration of flowering is mediated by red light. Finally, we discuss advances and perspectives for research on the perception of photoperiod in temperate grasses.more » « less
-
Summary Alfalfa (
Medicago sativa L.) is a perennial flowering plant in the legume family that is widely cultivated as a forage crop for its high yield, forage quality and related agricultural and economic benefits. Alfalfa is a photoperiod sensitive long‐day (LD) plant that can accomplish its vegetative and reproductive phases in a short period of time. However, rapid flowering can compromise forage biomass yield and quality. Here, we attempted to delay flowering in alfalfa using multiplex CRISPR/Cas9‐mediated mutagenesis ofFLOWERING LOCUS Ta1 (MsFTa1 ), a key floral integrator and activator gene. Four guide RNAs (gRNAs) were designed and clustered in a polycistronic tRNA–gRNA system and introduced into alfalfa byAgrobacterium ‐mediated transformation. Ninety‐six putative mutant lines were identified by gene sequencing and characterized for delayed flowering time and related desirable agronomic traits. Phenotype assessment of flowering time under LD conditions identified 22 independent mutant lines with delayed flowering compared to the control. Six independentMsfta1 lines containing mutations in all four copies ofMsFTa1 accumulated significantly higher forage biomass yield, with increases of up to 78% in fresh weight and 76% in dry weight compared to controls. Depending on the harvesting schemes, many of these lines also had reduced lignin, acid detergent fibre (ADF) and neutral detergent fibre (NDF) content and significantly higher crude protein (CP) and mineral contents compared to control plants, especially in the stems. These CRISPR/Cas9‐editedMsfta1 mutants could be introduced in alfalfa breeding programmes to generate elite transgene‐free alfalfa cultivars with improved forage biomass yield and quality. -
Abstract Flowering is a key developmental transition in the plant life cycle. In temperate climates, flowering often occurs in response to the perception of seasonal cues such as changes in day-length and temperature. However, the mechanisms that have evolved to control the timing of flowering in temperate grasses are not fully understood. We identified a Brachypodium distachyon mutant whose flowering is delayed under inductive long-day conditions due to a mutation in the JMJ1 gene, which encodes a Jumonji domain-containing protein. JMJ1 is a histone demethylase that mainly demethylates H3K4me2 and H3K4me3 in vitro and in vivo. Analysis of the genome-wide distribution of H3K4me1, H3K4me2, and H3K4me3 in wild-type plants by chromatin immunoprecipitation and sequencing combined with RNA sequencing revealed that H3K4m1 and H3K4me3 are positively associated with gene transcript levels, whereas H3K4me2 is negatively correlated with transcript levels. Furthermore, JMJ1 directly binds to the chromatin of the flowering regulator genes VRN1 and ID1 and affects their transcription by modifying their H3K4me2 and H3K4me3 levels. Genetic analyses indicated that JMJ1 promotes flowering by activating VRN1 expression. Our study reveals a role for JMJ1-mediated chromatin modification in the proper timing of flowering in B. distachyon.
-
Summary Many plants require prolonged exposure to cold to acquire the competence to flower. The process by which cold exposure results in competence is known as vernalization. In
Arabidopsis thaliana , vernalization leads to the stable repression of the floral repressor via chromatin modification, including an increase of trimethylation on lysine 27 of histone H3 (H3K27me3) by Polycomb Repressive Complex 2 (FLOWERING LOCUS CPRC 2). Vernalization in pooids is associated with the stable induction of a floral promoter, (VERNALIZATION 1VRN1 ). From a screen for mutants with a reduced vernalization requirement in the model grassBrachypodium distachyon , we identified two recessive alleles of (ENHANCER OF ZESTE ‐LIKE 1 ).EZL 1 is orthologous toEZL 1A. thaliana , a gene that encodes the catalytic subunit ofCURLY LEAF 1PRC 2.B. distachyon ezl1 mutants flower rapidly without vernalization in long‐day (LD ) photoperiods; thus, is required for the proper maintenance of the vegetative state prior to vernalization. Transcriptomic studies inEZL 1ezl1 revealed mis‐regulation of thousands of genes, including ectopic expression of several floral homeotic genes in leaves. Loss of results in the global reduction of H3K27me3 and H3K27me2, consistent with this gene making a major contribution toEZL 1PRC 2 activity inB. distachyon . Furthermore, inezl1 mutants, the flowering genes andVRN 1 (AGAMOUS ) are ectopically expressed and have reduced H3K27me3. Artificial microAG RNA knock‐down of either orVRN 1 inAG ezl1‐1 mutants partially restores wild‐type flowering behavior in non‐vernalized plants, suggesting that ectopic expression inezl1 mutants may contribute to the rapid‐flowering phenotype. -
SUMMARY Flowering of the reference legume
Medicago truncatula is promoted by winter cold (vernalization) followed by long‐day photoperiods (VLD) similar to winter annual Arabidopsis. However, Medicago lacksFLC andCO , key regulators of Arabidopsis VLD flowering. Most plants have twoINHIBITOR OF GROWTH (ING ) genes (ING1 andING2 ), encoding proteins with an ING domain with two anti‐parallel alpha‐helices and a plant homeodomain (PHD) finger, but their genetic role has not been previously described. In Medicago,Mting1 gene‐edited mutants developed and flowered normally, but anMting2‐1 Tnt1 insertion mutant and gene‐editedMting2 mutants had developmental abnormalities including delayed flowering particularly in VLD, compact architecture, abnormal leaves with extra leaflets but no trichomes, and smaller seeds and barrels.Mting2 mutants had reduced expression of activators of flowering, including theFT ‐like geneMtFTa1 , and increased expression of the candidate repressorMtTFL1c , consistent with the delayed flowering of the mutant.MtING2 overexpression complementedMting2‐1 , but did not accelerate flowering in wild type. The MtING2 PHD finger bound H3K4me2/3 peptides weaklyin vitro , but analysis of gene‐edited mutants indicated that it was dispensable to MtING2 function in wild‐type plants. RNA sequencing experiments indicated that >7000 genes are mis‐expressed in theMting2‐1 mutant, consistent with its strong mutant phenotypes. Interestingly, ChIP‐seq analysis identified >5000 novel H3K4me3 locations in the genome ofMting2‐1 mutants compared to wild type R108. Overall, our mutant study has uncovered an important physiological role of a plantING2 gene in development, flowering, and gene expression, which likely involves an epigenetic mechanism.