Homology-dependent gene silencing in transgenic plants: epistatic silencing loci contain multiple copies of methylated transgenes

• Published in: Molecular & general genetics Vol. 244; no. 3; p. 219
• Main Authors: Matzke, A J, Neuhuber, F, Park, Y D, Ambros, P F, Matzke, M A
• Format: Journal Article
• Language: English
• Published: Germany 02-08-1994
• Subjects: Alleles; Amino Acid Oxidoreductases - genetics; Chromosome Mapping; DNA Modification Methylases - metabolism; Epistasis, Genetic; Gene Expression Regulation; Genes, Plant - genetics; Genes, Regulator - genetics; In Situ Hybridization; Methylation; Models, Genetic; Multigene Family - genetics; Nicotiana - genetics; Plants, Genetically Modified; Plants, Toxic; Promoter Regions, Genetic - genetics; Sequence Homology, Nucleic Acid
• ISSN: 0026-8925
• DOI: 10.1007/bf00285449

Previous work has shown that two homologous, unlinked transgene loci can interact in plant nuclei, leading to non-reciprocal trans-inactivation and methylation of genes at one locus. Here, we report the structure and methylation of different transgene loci that contain the same construct but are variably able to inactivate and methylate a partially homologous, unlinked target locus. Silencing loci comprised multiple, methylated copies of the transgene construct, whereas a non-silencing locus contained a single, unmethylated copy. The correspondence between strength of silencing activity and copy number/degree of methylation was further demonstrated by producing novel alleles of a strong silencing locus: reducing the transgene copy number and methylation within this silencing locus decreased its ability to inactivate the target locus. The strong silencing locus, which was located close to a telomere, trans-inactivated various structural variants of the original target construct, regardless of their location in the genome. This suggests that the silencing locus can scan the entire genome for homologous regions, a process possibly aided by its telomeric location. Our data support the idea that epistatic trans-inactivation of unlinked, homologous transgenes in plants results from a pre-existing epigenetic difference between transgene loci, which is subsequently equalized by "epigene conversion" involving DNA-DNA pairing.