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1.
New Phytol ; 217(2): 871-882, 2018 01.
Article in English | MEDLINE | ID: mdl-29034954

ABSTRACT

Parental environments can influence offspring traits. However, the magnitude of the impact of parental environments on offspring molecular phenotypes is poorly understood. Here, we test the direct effects and intergenerational effects of jasmonic acid (JA) treatment, which is involved in herbivory-induced defense signaling, on transcriptomes and metabolomes in apomictic common dandelion (Taraxacum officinale). In a full factorial crossed design with parental and offspring JA and control treatments, we performed leaf RNA-seq gene expression analysis, LC-MS metabolomics and total phenolics assays in offspring plants. Expression analysis, leveraged by a de novo assembled transcriptome, revealed an induced response to JA exposure that is consistent with known JA effects. The intergenerational effect of treatment was considerable: 307 of 858 detected JA-responsive transcripts were affected by parental JA treatment. In terms of the numbers of metabolites affected, the magnitude of the chemical response to parental JA exposure was c. 10% of the direct JA treatment response. Transcriptome and metabolome analyses both identified the phosphatidylinositol signaling pathway as a target of intergenerational JA effects. Our results highlight that parental environments can have substantial effects in offspring generations. Transcriptome and metabolome assays provide a basis for zooming in on the potential mechanisms of inherited JA effects.


Subject(s)
Apomixis/genetics , Cyclopentanes/pharmacology , Environment , Metabolome/genetics , Oxylipins/pharmacology , Taraxacum/genetics , Taraxacum/metabolism , Transcriptome/genetics , Apomixis/drug effects , Cluster Analysis , Gene Expression Regulation, Plant/drug effects , Gene Ontology , Metabolome/drug effects , Metabolomics , Phenols/metabolism , Plant Leaves/drug effects , Plant Leaves/metabolism , Taraxacum/drug effects , Transcriptome/drug effects
2.
Planta ; 239(1): 199-212, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24142112

ABSTRACT

The inheritance of glyphosate resistance in two Amaranthus palmeri populations (R1 and R2) was examined in reciprocal crosses (RC) and second reciprocal crosses (2RC) between glyphosate-resistant (R) and -susceptible (S) parents of this dioecious species. R populations and Female-R × Male-S crosses contain higher 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene copy numbers than the S population. EPSPS expression, EPSPS enzyme activity, EPSPS protein quantity, and level of resistance to glyphosate correlated positively with genomic EPSPS relative copy number. Transfer of resistance was more influenced by the female than the male parent in spite of the fact that the multiple copies of EPSPS are amplified in the nuclear genome. This led us to hypothesize that this perplexing pattern of inheritance may result from apomictic seed production in A. palmeri. We confirmed that reproductively isolated R and S female plants produced seeds, indicating that A. palmeri can produce seeds both sexually and apomictically (facultative apomixis). This apomictic trait accounts for the low copy number inheritance in the Female-S × Male-R offsprings. Apomixis may also enhance the stability of the glyphosate resistance trait in the R populations in the absence of reproductive partners.


Subject(s)
3-Phosphoshikimate 1-Carboxyvinyltransferase/genetics , Amaranthus/drug effects , Amaranthus/genetics , Apomixis/genetics , Glycine/analogs & derivatives , 3-Phosphoshikimate 1-Carboxyvinyltransferase/metabolism , Apomixis/drug effects , Drug Resistance/genetics , Gene Amplification , Gene Dosage , Gene Expression Regulation, Plant , Genetic Variation , Glycine/pharmacology , Herbicides/pharmacology , Plant Proteins/genetics , Plant Proteins/metabolism , Glyphosate
3.
J Exp Bot ; 63(8): 3229-41, 2012 May.
Article in English | MEDLINE | ID: mdl-22378948

ABSTRACT

Apomixis in Hieracium subgenus Pilosella initiates in ovules when sporophytic cells termed aposporous initial (AI) cells enlarge near sexual cells undergoing meiosis. AI cells displace the sexual structures and divide by mitosis to form unreduced embryo sac(s) without meiosis (apomeiosis) that initiate fertilization-independent embryo and endosperm development. In some Hieracium subgenus Pilosella species, these events are controlled by the dominant LOSS OF APOMEIOSIS (LOA) and LOSS OF PARTHENOGENESIS (LOP) loci. In H. praealtum and H. piloselloides, which both contain the same core LOA locus, the timing and frequency of AI cell formation is altered in derived mutants exhibiting abnormal funiculus growth and in transgenic plants expressing rolB which alters cellular sensitivity to auxin. The impact on apomictic and sexual reproduction was examined here when a chimeric RNAse gene was targeted to the funiculus and basal portions of the ovule, and also when polar auxin transport was inhibited during ovule development following N-1-naphthylphthalamic acid (NPA) application. Both treatments led to ovule deformity in the funiculus and distal parts of the ovule and LOA-dependent alterations in the timing, position, and frequency of AI cell formation. In the case of NPA treatment, this correlated with increased expression of DR5:GFP in the ovule, which marks the accumulation of the plant hormone auxin. Our results show that sporophytic information potentiated by funiculus growth and polar auxin transport influences ovule development, the initiation of apomixis, and the progression of embryo sac development in Hieracium. Signals associated with ovule pattern formation and auxin distribution or perception may influence the capacity of sporophytic ovule cells to respond to LOA.


Subject(s)
Apomixis/physiology , Asteraceae/growth & development , Ovule/growth & development , Apomixis/drug effects , Apomixis/genetics , Arabidopsis Proteins/metabolism , Asteraceae/cytology , Asteraceae/drug effects , Asteraceae/genetics , Biological Transport/drug effects , Cell Division/drug effects , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Gene Expression Regulation, Plant/drug effects , Genes, Plant/genetics , Genetic Loci/genetics , Germination/drug effects , Green Fluorescent Proteins/metabolism , Indoleacetic Acids/pharmacology , Organ Specificity/drug effects , Organ Specificity/genetics , Ovule/cytology , Ovule/drug effects , Ovule/genetics , Phenotype , Phthalimides/pharmacology , Plants, Genetically Modified , Ribonucleases/metabolism , Transformation, Genetic/drug effects
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