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Turra, G. M.

Publications and source records attributed to Turra, G. M..

2 recordsLinked to original sources

Insights from controlled, comparative experiments highlight the limitations of using BSMV and FoMV for virus-enabled reverse genetics in rice

1.Virus-enabled reverse genetics (VERG) is a powerful tool for transient gene expression modulation in plants, particularly where stable transformation is challenging. However, the efficacy of VERG varies across species. In this study, we tested two commonly used viral vectors, barley stripe mosaic virus (BSMV) and foxtail mosaic virus (FoMV), for their ability to induce virus-induced gene silencing (VIGS) and virus-mediated overexpression (VOX) in rice (Oryza sativa L.). While both vectors successfully altered gene expression in wheat (Triticum aestivum), they failed to do so in six rice cultivars from different subspecies, despite rigorous optimization of inoculation methods and environmental conditions. The BSMV vector carrying antisense phytoene desaturase (PDS) sequences did not induce the expected photobleaching phenotype, and FoMV-driven GFP expression was absent in rice. These findings contrast with previous reports of successful VERG in other monocots and suggest that intrinsic resistance mechanisms exist in rice which may inhibit or reduce viral vector efficacy. Our results highlight the species-specific limitations of VERG and underscore the need for alternative viral systems or novel vector designs for functional genomics research in rice. By sharing our unsuccessful attempts, we aim to prevent redundant efforts and encourage further exploration of VERG in Oryza species.

plant biology↗

Subgenome dominance of ALS target site mutations impacts herbicide resistance in allohexaploid Echinochloa crus-galli

Herbicide target site resistance in polyploid species is more complex than diploids due to potential subgenome interactions and gene dosage of mutations. The objective of this study was to identify the level of resistance and cross-resistance patterns of ALS mutations located in the different subgenomes of allohexaploid Echinochloa crus-galli. E. crus-galli populations were screened and dose-response curves were performed with ALS-inhibitors from different chemical groups. The ALS genes of each subgenome (A, B, and C) were sequenced. Copy number variation, global relative expression, and the specific relative expression of ALS gene from each subgenome were performed. Out of 100 populations, 32% were resistant only to imazethapyr, and 48% were cross-resistant to all ALS-inhibitors. The mutations Ala122Thr, Ala205Asn, and Ser653Asn confer resistance only to imazethapyr, while Trp574Leu confers resistance to all four herbicides tested. ALS mutations were most frequent in subgenome A, but ALS from subgenome C had the highest expression. The biotype SAOJER-01 had Trp574Leu mutation in subgenome C and was 22 times more resistant to imazethapyr and penoxsulam than CAMAQ-01, which had the same Trp574Leu mutation in subgenome A with no differences in herbicide metabolism rate. The ALS genes from subgenomes A and C contribute approximately 13% and 50% respectively to the total ALS transcripts. The higher contribution of subgenome C to the total ALS transcripts pool combined with the Trp574Leu resistance mutation makes the biotype SAOJER-01 more resistant to herbicides than CAMAQ-01. This is the first study showing the effect of subgenome gene expression level on the herbicide resistance level in a polyploid weed species. In addition, while imazethapyr did not control any biotype with an ALS mutation, the other ALS-inhibitor herbicides were able to control biotypes carrying Ala122Thr, Ala205Asn, and Ser653Asn, which reinforces the utility of these herbicides in weed and resistance management.

genetics↗