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Joly, V.

Publications and source records attributed to Joly, V..

2 recordsLinked to original sources

Differential gene expression analysis identifies a group of defensin like peptides from Solanum chacoense ovules with in vitro pollen tube attraction activity

Solanum chacoense is a wild potato species with superior genetic resistance to diseases and pests that has been extensively used for introgression into cultivated potato. One determinant of crossing success between wild and cultivated potato species is the effective ploidy of the parents. However, little is known about whether other, prezygotic level, breeding barriers exist. We hypothesize ovular pollen tube guidance may serve as such a checkpoint. Tests for species-specific pollen tube guidance using semi-in vivo assays suggested a positive correlation between species-specificity and taxonomic distance. RNA-seq of ovules hand dissected from wild type plants at anthesis and two days before anthesis, as well as from a frk1 mutant lacking an embryo sac identified a list of 284 embryo sac-dependent genes highly expressed in mature ovules and poorly expressed in all other samples. Among these are 17 Solanum chacoense cysteine-rich proteins (ScCRPs), considered to be good candidates since CRPs are ovular pollen tube attractants in other species. A group of three cloned and purified ScCRP2 sequences belonging to the DEFL protein family showed moderate levels of in vitro pollen tube attraction activity in functional assays. We conclude that ScCRP2s are good candidates for ovular pollen tube guidance in S. chacoense. HighlightsThis work introduces key characteristics of pollen tube guidance in Solanum chacoense, identifies candidate attractants through transcriptome subtraction and reports in vitro pollen tube attraction activity for three defensin-like peptides.

plant biology↗

H3.1K27me1 maintains transcriptional silencing and genome stability by preventing GCN5-mediated histone acetylation

In plants, genome stability is maintained during DNA replication by the H3.1K27 methyltransferases ATXR5 and ATXR6, which catalyze the deposition of K27me1 on replicationdependent H3.1 variants. Loss of H3.1K27me1 in atxr5 atxr6 double mutants leads to heterochromatin defects, including transcriptional de-repression and genomic instability, but the molecular mechanisms involved remain largely unknown. In this study, we identified the conserved histone acetyltransferase GCN5 as a mediator of transcriptional de-repression and genomic instability in the absence of H3.1K27me1. GCN5 is part of a SAGA-like complex in plants that requires ADA2b and CHR6 to mediate the heterochromatic defects of atxr5 atxr6 mutants. Our results show that Arabidopsis GCN5 acetylates multiple lysine residues on H3.1 variants in vitro, but that H3.1K27 and H3.1K36 play key roles in inducing genomic instability in the absence of H3.1K27me1. Overall, this work reveals a key molecular role for H3.1K27me1 in maintaining genome stability by restricting histone acetylation in plants.

plant biology↗