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      Did apomixis evolve from sex or was it the other way around?

      1 , 2 , 3 , 4
      Journal of Experimental Botany
      Oxford University Press (OUP)

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          Understanding mechanisms of novel gene expression in polyploids.

          Polyploidy has long been recognized as a prominent force shaping the evolution of eukaryotes, especially flowering plants. New phenotypes often arise with polyploid formation and can contribute to the success of polyploids in nature or their selection for use in agriculture. Although the causes of novel variation in polyploids are not well understood, they could involve changes in gene expression through increased variation in dosage-regulated gene expression, altered regulatory interactions, and rapid genetic and epigenetic changes. New research approaches are being used to study these mechanisms and the results should provide a more complete understanding of polyploidy.
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            Ethylene Response Factors: A Key Regulatory Hub in Hormone and Stress Signaling.

            Ethylene is essential for many developmental processes and a key mediator of biotic and abiotic stress responses in plants. The ethylene signaling and response pathway includes Ethylene Response Factors (ERFs), which belong to the transcription factor family APETALA2/ERF. It is well known that ERFs regulate molecular response to pathogen attack by binding to sequences containing AGCCGCC motifs (the GCC box), a cis-acting element. However, recent studies suggest that several ERFs also bind to dehydration-responsive elements and act as a key regulatory hub in plant responses to abiotic stresses. Here, we review some of the recent advances in our understanding of the ethylene signaling and response pathway, with emphasis on ERFs and their role in hormone cross talk and redox signaling under abiotic stresses. We conclude that ERFs act as a key regulatory hub, integrating ethylene, abscisic acid, jasmonate, and redox signaling in the plant response to a number of abiotic stresses.
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              Stress-induced DNA methylation changes and their heritability in asexual dandelions.

              *DNA methylation can cause heritable phenotypic modifications in the absence of changes in DNA sequence. Environmental stresses can trigger methylation changes and this may have evolutionary consequences, even in the absence of sequence variation. However, it remains largely unknown to what extent environmentally induced methylation changes are transmitted to offspring, and whether observed methylation variation is truly independent or a downstream consequence of genetic variation between individuals. *Genetically identical apomictic dandelion (Taraxacum officinale) plants were exposed to different ecological stresses, and apomictic offspring were raised in a common unstressed environment. We used methylation-sensitive amplified fragment length polymorphism markers to screen genome-wide methylation alterations triggered by stress treatments and to assess the heritability of induced changes. *Various stresses, most notably chemical induction of herbivore and pathogen defenses, triggered considerable methylation variation throughout the genome. Many modifications were faithfully transmitted to offspring. Stresses caused some epigenetic divergence between treatment and controls, but also increased epigenetic variation among plants within treatments. *These results show the following. First, stress-induced methylation changes are common and are mostly heritable. Second, sequence-independent, autonomous methylation variation is readily generated. This highlights the potential of epigenetic inheritance to play an independent role in evolutionary processes, which is superimposed on the system of genetic inheritance.
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                Author and article information

                Journal
                Journal of Experimental Botany
                Oxford University Press (OUP)
                0022-0957
                1460-2431
                May 15 2019
                June 01 2019
                March 11 2019
                May 15 2019
                June 01 2019
                March 11 2019
                : 70
                : 11
                : 2951-2964
                Affiliations
                [1 ]Department of Agricultural, Food and Environmental Sciences, University of Perugia, Perugia, Italy
                [2 ]Laboratory of Genomics, Department of Agronomy, Food, Natural Resources, Animals and the Environment (DAFNAE), University of Padova Legnaro, PD, Italy
                [3 ]Department of Plants, Soils and Climate, Utah State University, Logan, Utah, USA
                [4 ]Institute of Biosciences and Bioresources, Research Division of Perugia, National Research Council (CNR), Perugia, Italy
                Article
                10.1093/jxb/erz109
                30854543
                24e7f805-2365-4fcd-b5e0-2bdef22c9cfa
                © 2019

                https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

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