Segregation of an MSH1 RNAi transgene produces heritable non-genetic memory in association with methylome reprogramming

Autor: Robersy Sanchez, Rosemary Schwegel, Kamaldeep S. Virdi, Xiaodong Yang, Tom Maher, Michael J. Axtell, Hardik Kundariya, Sally A. Mackenzie, Isaac J. Dopp
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0106 biological sciences
0301 basic medicine
Cellular signalling networks
Plant genetics
Transgene
Science
Circadian clock
Arabidopsis
Inheritance Patterns
Gene regulatory network
General Physics and Astronomy
Biology
Histone Deacetylase 6
01 natural sciences
Article
General Biochemistry
Genetics and Molecular Biology

Epigenesis
Genetic

03 medical and health sciences
Quantitative Trait
Heritable

RNA interference
Gene Regulatory Networks
DNA (Cytosine-5-)-Methyltransferases
Transgenes
lcsh:Science
Genetic memory (biology)
Genetics
DNA methylation
Multidisciplinary
Arabidopsis Proteins
Gene Expression Profiling
General Chemistry
Methylation
Plants
Genetically Modified

Adaptation
Physiological

MutS DNA Mismatch-Binding Protein
Gene Ontology
030104 developmental biology
RNA Interference
lcsh:Q
Reprogramming
Genome-Wide Association Study
Signal Transduction
010606 plant biology & botany
Zdroj: Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Nature Communications
ISSN: 2041-1723
Popis: MSH1 is a plant-specific protein. RNAi suppression of MSH1 results in phenotype variability for developmental and stress response pathways. Segregation of the RNAi transgene produces non-genetic msh1 ‘memory’ with multi-generational inheritance. First-generation memory versus non-memory comparison, and six-generation inheritance studies, identifies gene-associated, heritable methylation repatterning. Genome-wide methylome analysis integrated with RNAseq and network-based enrichment studies identifies altered circadian clock networks, and phytohormone and stress response pathways that intersect with circadian control. A total of 373 differentially methylated loci comprising these networks are sufficient to discriminate memory from nonmemory full sibs. Methylation inhibitor 5-azacytidine diminishes the differences between memory and wild type for growth, gene expression and methylation patterning. The msh1 reprogramming is dependent on functional HISTONE DEACETYLASE 6 and methyltransferase MET1, and transition to memory requires the RNA-directed DNA methylation pathway. This system of phenotypic plasticity may serve as a potent model for defining accelerated plant adaptation during environmental change.
Segregation of an MSH1 RNAi transgene produces non-genetic memory that displays transgenerational inheritance in Arabidopsis. Here, the authors compare memory and non-memory full-sib progenies to show the involvement of DNA methylation reprogramming, involving the RdDM pathway, in transition to a heritable memory state.
Databáze: OpenAIRE