Evidence map›Paper›PMID 40993522›Full record

ArticleBMC plant biology2025

Spatio-temporal regulation of recombinase expression enables efficient autoexcision of selectable marker genes in soybean and maize.

Brent O'Brien, Anagha Sant, Lisa Kanizay, Stanislaw Flasinski, Olivia Haragutchi, Xudong Ye, Anthony Paisley, Matthew S Marengo

Abstract read
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Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Brent O'BrienPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Anagha SantPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Lisa KanizayPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Stanislaw FlasinskiPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Olivia HaragutchiPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Xudong YePlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Anthony PaisleyPlant Biotechnology, Bayer Crop Science, Chesterfield, United States.
Matthew S MarengoPlant Biotechnology, Bayer Crop Science, Chesterfield, United States. matt.marengo@bayer.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost plant transformation protocols include the use of a selectable marker gene to enable efficient selection of transformed cells for transgenic regeneration. While the marker gene facilitates the transformation process, it is not needed once transgenic plants have been identified and is removed during commercial development. Autoexcision is a marker removal process, in which a Cre-lox system is used to remove both the selectable marker gene and the Cre gene itself in the T0 generation. One challenge for autoexcision is achieving efficient marker removal while preserving the recovery rate for transgene-positive transformation events. Predictable and robust control of Cre gene expression is essential to maintaining this balance.

resultsIn this report, we demonstrate the utility of promoters and other expression elements that were selected based on the RNA-seq-derived, tissue-specific expression patterns of their associated endogenous genes. These elements were selected for their potential to drive Cre in a specific spatio-temporal manner. Functional elements expected to drive Cre primarily in floral meristem, gametes, and/or early embryo enabled efficient autoexcision and recovery of transgenic transformants. Additionally, we confirmed the expected expression patterns of successful elements via GUS staining.

conclusionsOverall, these elements enable an efficient approach for selectable marker gene removal during commercial development.

Indexed as

Glycine maxIntegrasesZea maysGene Expression Regulation, PlantGenes, PlantGenetic MarkersPlants, Genetically ModifiedPromoter Regions, GeneticTransformation, GeneticCre recombinaseGenetic MarkersIntegrasesAutoexcisionCreGene expressionGlycine maxSelectable markerZea mays

Identifiers

PMID40993522
PMCPMC12461952

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.