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Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
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Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
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Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants

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Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants
Journal Article

Genomic and Epigenomic Changes in the Progeny of Cold-Stressed IArabidopsis thaliana/I Plants

2024
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Overview
Plants are continuously exposed to various environmental stresses. Because they can not escape stress, they have to develop mechanisms of remembering stress exposures somatically and passing it to the progeny. We studied the Arabidopsis thaliana ecotype Columbia plants exposed to cold stress for 25 continuous generations. Our study revealed that multigenerational exposure to cold stress resulted in the changes in the genome and epigenome (DNA methylation) across generations. Main changes in the progeny were due to the high frequency of genetic mutations rather than epigenetic changes; the difference was primarily in single nucleotide substitutions and deletions. The progeny of cold-stressed plants exhibited the higher rate of missense non-synonymous mutations as compared to the progeny of control plants. At the same time, epigenetic changes were more common in the CHG (C = cytosine, H = cytosine, adenine or thymine, G = guanine) and CHH contexts and favored hypomethylation. There was an increase in the frequency of C to T (thymine) transitions at the CHH positions in the progeny of cold stressed plants; because this type of mutations is often due to the deamination of the methylated cytosines, it can be hypothesized that environment-induced changes in methylation contribute to mutagenesis and may be to microevolution processes and that RNA-dependent DNA methylation plays a crucial role. Our work supports the existence of heritable stress response in plants and demonstrates that genetic changes prevail.