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1.
Genome Biol ; 22(1): 141, 2021 05 06.
Artículo en Inglés | MEDLINE | ID: mdl-33957942

RESUMEN

BACKGROUND: Hybridization of plants that differ in number of chromosome sets (ploidy) frequently causes endosperm failure and seed arrest, a phenomenon referred to as triploid block. In Arabidopsis, loss of function of NRPD1, encoding the largest subunit of the plant-specific RNA polymerase IV (Pol IV), can suppress the triploid block. Pol IV generates short RNAs required to guide de novo methylation in the RNA-directed DNA methylation (RdDM) pathway. Recent work suggests that suppression of the triploid block by mutants in RdDM components differs, depending on whether the diploid pollen is derived from tetraploid plants or from the omission in second division 1 (osd1) mutant. This study aims to understand this difference. RESULTS: In this study, we find that the ability of mutants in the RdDM pathway to suppress the triploid block depends on their degree of inbreeding. While first homozygous generation mutants in RdDM components NRPD1, RDR2, NRPE1, and DRM2 have weak or no ability to rescue the triploid block, they are able to suppress the triploid block with successive generations of inbreeding. Inbreeding of nrpd1 was connected with a transgenerational loss of non-CG DNA methylation on sites jointly regulated by CHROMOMETHYLASES 2 and 3. CONCLUSIONS: Our data reveal that loss of RdDM function differs in its effect in early and late generations, which has important implications when interpreting the effect of RdDM mutants.


Asunto(s)
Arabidopsis/genética , Metilación de ADN/genética , Mutación/genética , ARN de Planta/metabolismo , Triploidía , Arabidopsis/embriología , Regulación de la Expresión Génica de las Plantas , Genes de Plantas , Endogamia , ARN de Planta/genética , Semillas/genética
2.
PLoS Genet ; 17(2): e1009370, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-33571184

RESUMEN

Hybridization of closely related plant species is frequently connected to endosperm arrest and seed failure, for reasons that remain to be identified. In this study, we investigated the molecular events accompanying seed failure in hybrids of the closely related species pair Capsella rubella and C. grandiflora. Mapping of QTL for the underlying cause of hybrid incompatibility in Capsella identified three QTL that were close to pericentromeric regions. We investigated whether there are specific changes in heterochromatin associated with interspecific hybridizations and found a strong reduction of chromatin condensation in the endosperm, connected with a strong loss of CHG and CHH methylation and random loss of a single chromosome. Consistent with reduced DNA methylation in the hybrid endosperm, we found a disproportionate deregulation of genes located close to pericentromeric regions, suggesting that reduced DNA methylation allows access of transcription factors to targets located in heterochromatic regions. Since the identified QTL were also associated with pericentromeric regions, we propose that relaxation of heterochromatin in response to interspecies hybridization exposes and activates loci leading to hybrid seed failure.


Asunto(s)
Capsella/genética , Cromatina/genética , Endospermo/genética , Hibridación Genética , Semillas/genética , Capsella/clasificación , Centrómero/genética , Cromatina/metabolismo , Aberraciones Cromosómicas , Metilación de ADN , Regulación de la Expresión Génica de las Plantas , Genes de Plantas/genética , Heterocromatina/genética , Heterocromatina/metabolismo , Sitios de Carácter Cuantitativo/genética , Especificidad de la Especie
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