EPSPS Gene Research Articles

EPSPS gene amplification in a glyphosate-resistant population of Italian ryegrass (Lolium multiflorum) from Oregon.

Lolium multiflorum Lam. (Italian ryegrass, annual ryegrass) is both a weed and a crop in Oregon. Because it is commonly managed using chemical controls, herbicide-resistant populations have evolved within the seed production region. A glyphosate-resistant population was identified in Yamhill County, Oregon, in a fallow field previously cropped with perennial ryegrass. Dose-response studies showed that the glyphosate-resistant population, OR12, was nine-fold more resistant to glyphosate than the susceptible population. No EPSPS amino acid substitutions known to confer glyphosate resistance were observed via gene sequencing. Quantitative polymerase chain reaction (qPCR) of genomic DNA revealed a mean 30-fold increase in EPSPS gene copies in the OR12 population. Biomass after glyphosate treatment was correlated with EPSPS gene copy number of individual plants. This is the first known report of glyphosate resistance associated with EPSPS gene amplification to arise in L. multiflorum populations in Oregon. © 2024 Society of Chemical Industry. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Confirmation of glyphosate-resistant Palmer amaranth (Amaranthus palmeri) populations in New York and responses to alternative chemistries

Abstract Palmer amaranth (Amaranthus palmeri S. Watson, AMAPA) is one of the most troublesome weeds in North America due to its rapid growth rate, substantial seed production, competitiveness and the evolution of herbicide-resistant populations. Though frequently encountered in the South, Midwest, and Mid-Atlantic regions of the United States, A. palmeri was recently identified in soybean [Glycine max (L.) Merr.] fields in Genesee, Orange, and Steuben counties, NY, where glyphosate was the primary herbicide for in-crop weed control. This research, conducted in 2023, aimed to (1) describe the dose response of three putative resistant NY A. palmeri populations to glyphosate, (2) determine their mechanisms of resistance, and (3) assess their sensitivity to other postemergence herbicides commonly used in NY crop production systems. Based on the effective dose necessary to reduce aboveground biomass by 50% (ED50), the NY populations were 42 to 67 times more resistant to glyphosate compared with a glyphosate-susceptible population. Additionally, the NY populations had elevated EPSPS gene copy numbers ranging from 25 to 135 located within extrachromosomal circular DNA (eccDNA). Label rate applications of Weed Science Society of America (WSSA) Group 2 herbicides killed up to 42% of the NY populations of A. palmeri. Some variability was observed among populations in response to WSSA Group 5 and 27 herbicides. All populations were effectively controlled by labeled rates of herbicides belonging to WSSA Groups 4, 10, 14, and 22. Additional research is warranted to confirm whether NY populations have evolved multiple resistance to herbicides within other WSSA groups and to develop effective A. palmeri management strategies suitable for NY crop production.

Glyphosate Resistance in Eleusine indica: Involvement of CYP71AK44 in Addition to EPSPS Gene Overexpression.

Intensive application of glyphosate has resulted in resistance evolution in many weed populations, including Eleusine indica. This study characterized glyphosate resistance and investigated the underlying mechanisms in a glyphosate-resistant population (R-JX) of E. indica from China. The R-JX population was 8.5 times resistant to glyphosate relative to the glyphosate-susceptible population (SA). Point mutations were not observed in the target gene 5-enolypyruvyl-shikimate-3-phosphate synthase gene (EPSPS). However, the expression level and copy number of EPSPS were 8.8 times and 15.2 times, respectively, greater in R-JX than that in the SA population. Pre-application of the P450 inhibitor lowered the resistance level to glyphosate from 8.5 times to 3.6 times in the R-JX population. RNA-Seq and RT-qPCR revealed that the CYP71AK44 gene was consistently upregulated in R-JX and five other glyphosate-resistant populations. Rice calli and seedlings overexpressing CYP71AK44 showed glyphosate resistance. In conclusion, overexpression of the target EPSPS plus CYP71AK44 collectively contributes to glyphosate resistance in these E. indica populations.

Unraveling the mechanisms of multiple resistance across glyphosate and glufosinate in Eleusine indica

The herbicides glyphosate and glufosinate are commonly used in citrus and sugarcane orchards in Guangxi Province, China, wherein the C4 plant Eleusine indica (L.) Gaertn. is known to be a dominant weed species. However, high selection pressure has resulted in failure of control. In the present study, experiments were conducted to clarify resistance levels for the suspected populations and elucidate the mechanisms for multiple resistance. The resistance index to glyphosate was calculated for eight populations and ranged from 5.4 to 21.3, with a low-level shikimate content of 0.24–0.50 μg g−1. In addition, three populations showed low-level resistance to glufosinate, with a resistance index ranging from 2.6 to 3.9. The amplification of the 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene with a double-mutation T102I + P106S (TIPS) or a single-mutation (P106S and P106A) was observed in most populations. The target genes of glufosinate (GS1–1, GS1–2, and GS1–3) showed high-level expression, namely 145.5-fold that of susceptible plants. The content of EPSPS and glutamine synthetase (GS) protein in resistant plants can reach to 3.6 and 2.1 times higher than those in susceptible plants, respectively. The overexpression of the EPSPS gene with double (T102I + P106S) or single (P106S and P106A) mutations, plus the overexpression of GS1–1, GS1–2, and GS1–3, responded to multiple resistance mechanisms. Altogether, these results demonstrate that overexpression of GS1 is a novel form of resistant mechanism to glufosinate in weeds.

Development of a double-antibody sandwich ELISA for quantification of mutated EPSPS gene expression in rice

Glyphosate resistance is a critically important trait for genetically modified (GM) crops. Mutation of the rice EPSPS gene results in a high level of glyphosate resistance, presenting significant potential for the development of glyphosate-tolerant crops. The resistance of rice to glyphosate is correlated with the expression levels of resistance genes. Therefore, developing a convenient, stable, and sensitive method for quantifying the OsmEPSPS protein is crucial for the development of glyphosate-resistant crops. We developed a double-antibody sandwich quantitative ELISA (DAS-ELISA) using a specific monoclonal antibody (mAb) for OsmEPSPS capture and an HRP-conjugated anti-OsmEPSPS rabbit polyclonal antibody (pAb). The method could be used to detect OsmEPSPS within a linear range of 16–256 ng/mL with robust intra- and inter-batch duplicability (%CV values: 0.17 %–7.24 %). OsmEPSPS expression in the transgenic rice lines (54.44–445.80 μg/g) was quantified using the DAS-ELISA. Furthermore, the expression of the OsmEPSPS gene was validated through Western blotting. This study demonstrated the reliability and stability of the DAS-ELISA for OsmEPSPS detection in GM rice.

Glyphosate resistance and no fitness cost in backcross offspring of wild soybean and transgenic soybean with epsps gene

BackgroundThe commercial utilization of genetically modified soybeans has yielded substantial economic advantages. Nevertheless, the genetic drift towards wild soybeans is one of the main ecological risks that needs to be addressed. Previous experiments demonstrated the absence of fitness cost or florescence overlap in hybrid offspring resulting from the crossbreeding of transgenic soybean GTS40-3-2 and Zhengzhou wild soybeans. In this study, hybrid progeny was systematically crossed with wild soybeans to establish a backcross progeny system. This system was employed to evaluate the ecological risk associated with the backcross progeny of transgenic and wild soybeans.ResultsThe findings indicated that the offspring from the backcross exhibited glyphosate tolerance. Furthermore, the expression of foreign proteins in the backcross offspring was notably lower than in the transgenic soybean, and there was no significant difference when compared to the hybrid progeny. Parameters such as germination rate, aboveground biomass, pods per plant, full seeds per plant, and 100-grain weight exhibited no significant differences between the negative and positive lines of the backcross progenies, and no fitness cost was identified in comparison to wild soybeans. These results underscore the potential for foreign genes to propagate within other wild soybeans, which requires continuous attention.ConclusionsThe widespread adoption of genetically modified soybeans has undeniably led to substantial economic gains. However, the research findings emphasize the critical importance of addressing the ecological risks posed by genetic drift towards wild soybeans. The backcross progeny system established in this study indicates that the potential for foreign gene dissemination to wild soybean populations warrants continued attention and mitigation strategies.

Adaptation to Environmental Stressors Conferred by Gene Copy Number Variation in Herbicide Resistant Amaranthus palmeri

Many rampant agricultural weeds have been found to contain gene copy number variation, a genetic adaptation that can facilitate the evolution of stress resistance. Amaranthus palmeri is a highly competitive and problematic agricultural weed in the United States which continues to naturalize, spreading northward to Canada. A.palmeri has gained attention due to its rapid evolution of herbicide resistance— a mechanism conferred by gene copy number variation of EPSPS. Researchers hypothesize that this gene is contained within an amplicon alongside other stress tolerance related genes. This raises the question of whether increased EPSPS gene copy number is associated with higher tolerance to environmental stressors, beyond herbicide stress. To prepare for addressing this hypothesis, I conducted a pilot project testing the ideal conditions for germination of A.palmeri. I planted 200 seeds divided between greenhouse and growth chamber environments. Many seeds benefit from a period of cold as a signal to break dormancy, thus, each category was further divided into two treatments: control and cold stratified (seeds were incubated in a –23 cold room for a week). I was interested in whether the increased consistency of temperature, light intensity, and photoperiod provided by a growth chamber, relative to a greenhouse, would increase germination rates. Results indicate that greenhouse grown seedlings had a 71% germination rate and within each treatment, 86% of cold stratified plants germinated while only 56% of the control group germinated. Whereas in the growth chamber, surprisingly only 26% of plants germinated with a breakdown of 22% cold stratified and 30% control. Thus, to germinate enough plants for a large-scale experiment, I chose to cold stratify seeds and grow them in the greenhouse for my undergraduate thesis. In this common garden experiment, I am currently growing 500 plants which will be divided into four stress treatment categories: control, salinity, drought, and salinity x drought. Using phenotypic measurements and digital droplet PCR (ddPCR) to quantify EPSPS gene copy number, I will test for a possible association between plants with a higher tolerance to these simulated environmental stressors and the presence of increased EPSPS gene copy number.

Optimizing molecular assays for glyphosate and ALS-inhibitor resistance diagnostics in four weed species

Herbicide-resistant weeds pose a threat to food production in modern agriculture, causing US$32 billion in crop production losses worldwide. In Michigan, highly troublesome and widespread weeds include waterhemp, Palmer amaranth, common ragweed, and horseweed, with accessions that are resistant to glyphosate (Group 9) and ALS-inhibitors (Group 2), major herbicide sites of action utilized in soybean and corn cropping systems. Molecular assays for rapid resistance diagnostics to confirm the in-field status of herbicide resistance can assist with more effective, timely, and proactive management. In this research, we developed and tested PCR-based assays to identify target site resistance mechanisms to both herbicide groups through Sanger sequencing and EPSPS copy number variation. Nine different SNPs were identified in five ALS positions known to confer herbicide resistance among all species surveyed. Pro197Ser was the most frequent in horseweed and common ragweed accessions, whereas Trp574Leu was the predominant mutation in Palmer amaranth and waterhemp. Four horseweed accessions contained the Pro106Ser mutation in the EPSPS gene, which confers resistance to glyphosate. Additionally, waterhemp and Palmer amaranth had 2–7 and 20–160 copies of EPSPS, respectively. The assays were validated by comparing genotyping of several field-collected accessions of unknown resistance status with known resistant and susceptible accessions. The efficacy of genotyping assays was >98% and required only two days, confirming that molecular assays are a robust tool for rapid resistance diagnostics. These assays can help growers evaluate herbicide resistance status in weed populations within the same growing season, allowing them to adopt effective management practices.

First report of target‐site resistance to glyphosate in Amaranthus hybridus L. in the Republic of South Africa

AbstractAmaranthus hybridus L. is a major weed for summer crops. Although A. hybridus has been a known crop weed in the Republic of South Africa (RSA) for a long time, herbicide resistance has not been a problem. Nevertheless, A. hybridus populations from KwaZulu Natal (KZN) Province have caught the attention of farmers since glyphosate has been progressively becoming less effective in controlling the species. This study aimed to evaluate herbicide resistance in A. hybridus and the underlying mechanisms of resistance. Seeds from 50 glyphosate‐resistant plants were collected from fields at Bergville and Winterton in KZN and compared with a susceptible population from Hendrina (Mpumalanga Province). Glasshouse screening was conducted where glyphosate (Roundup® PowerMax) was applied at 6‐leaf stage, at doses 0, 540, 1080 (recommended dose), 2160 and 4320 g ae ha−1. Surviving plants were sampled for molecular analysis to establish any target site mutations in the EPSPS gene that confer glyphosate resistance. Dose–response assay indicated 100% control in the Hendrina population, variation in the control of the Winterton population and 100% survival in the Bergville population. Molecular analysis indicated a rare triple mutation (TAP‐IVS) in the KZN populations. This kind of mutation endows a high level of glyphosate resistance, which explains why these populations survived even the 4× dose. These findings confirmed the first cases of glyphosate‐resistant A. hybridus and established the mechanism of resistance as target site mutations in the EPSPS gene reported in the RSA. These findings will serve as a base for other herbicide resistance cases and the development of initiatives to control and minimize the spread of this weed in the RSA.

The ancestral karyotype of the Heliantheae Alliance, herbicide resistance, and human allergens: Insights from the genomes of common and giant ragweed.

Ambrosia artemisiifolia and Ambrosia trifida (Asteraceae) are important pest species and the two greatest sources of aeroallergens globally. Here, we took advantage of a hybrid to simplify genome assembly and present chromosome-level assemblies for both species. These assemblies show high levels of completeness with Benchmarking Universal Single-Copy Ortholog (BUSCO) scores of 94.5% for A. artemisiifolia and 96.1% for A. trifida and long terminal repeat (LTR) Assembly Index values of 26.6 and 23.6, respectively. The genomes were annotated using RNA data identifying 41,642 genes in A. artemisiifolia and 50,203 in A. trifida. More than half of the genome is composed of repetitive elements, with 62% in A. artemisiifolia and 69% in A. trifida. Single copies of herbicide resistance-associated genes PPX2L, HPPD, and ALS were found, while two copies of the EPSPS gene were identified; this latter observation may reveal a possible mechanism of resistance to the herbicide glyphosate. Ten of the 12 main allergenicity genes were also localized, some forming clusters with several copies, especially in A. artemisiifolia. The evolution of genome structure has differed among these two species. The genome of A. trifida has undergone greater rearrangement, possibly the result of chromoplexy. In contrast, the genome of A. artemisiifolia retains a structure that makes the allotetraploidization of the most recent common ancestor of the Heliantheae Alliance the clearest feature of its genome. When compared to other Heliantheae Alliance species, this allowed us to reconstruct the common ancestor's karyotype-a key step for furthering of our understanding of the evolution and diversification of this economically and allergenically important group.

Unraveling the atomic mechanisms underlying glyphosate insensitivity in EPSPS: implications of distal mutations

5-enolpyruvyl shikimate-3-phosphate synthase (EPSPS), as an indispensable enzyme in the shikimate pathway, is the specific target of grasser killer glyphosate (GPJ). GPJ is a competitive inhibitor of phosphoenolpyruvate (PEP), which is the natural substrate of EPSPS. A novel Ls-EPSPS gene variant discovered from Liliaceae, named ELs-EPSPS, includes five distal mutations, E112V, D142N, T351S, D425G, and R496G, endowing high GPJ insensitivity. However, the implicit molecular mechanism of the enhanced tolerance/insensitivity of GPJ in ELs-EPSPS is not fully understood. Herein, we try to interpret the hidden molecular mechanism using computational methods. Computational results reveal the enhanced flexibility of apo EPSPS upon mutations. The enhanced affinity of the initial binding substrate shikimate-3-phosphate (S3P), and the higher probability of second ligands PEP/GPJ entering the pocket are observed in the ELs-EPSPS-S3P system. Docking and MD results further confirmed the decreased GPJ-induced EPSPS inhibition upon mutations. And, the alterations of K98 and R179 side-chain orientations upon mutations are detrimental to GPJ binding at the active site. Additionally, the oscillation of side chain K98, in charge of PEP location, improves the proximity effect for substrates in the dual-substrate systems upon mutations. Our results clarify that the enhanced GPJ tolerance of EPSPS is achieved from decreased competitive inhibition of GPJ at the atomic perspective, and this finding further contributes to the cultivation of EPSPS genes with higher GPJ tolerance/insensitivity and a mighty renovation for developing glyphosate-resistant crops. Communicated by Ramaswamy H. Sarma

EPSPS gene amplification confers glyphosate resistance in Palmer amaranth in Connecticut

Abstract A Palmer amaranth biotype (CT-Res) with resistance to glyphosate was recently confirmed in a pumpkin field in Connecticut. However, the underlying mechanisms conferring glyphosate resistance in this biotype is not known. The main objectives of this research were 1) to determine the effect of plant height (10, 20, and 30 cm) on glyphosate resistance levels in CT-Res Palmer amaranth biotype, and 2) to investigate whether the target site–based mechanisms confer glyphosate resistance. To achieve these objectives, progeny seeds of the CT-Res biotype after two generations of recurrent selection with glyphosate (6,720 g ae ha−1) were used. Similarly, known glyphosate-susceptible Palmer amaranth biotypes from Kansas (KS-Sus) and Alabama (AL-Sus) were included. Results from greenhouse dose-response studies revealed that CT-Res Palmer amaranth biotype had 69-, 64-, and 54-fold resistance to glyphosate as compared with the KS-Sus biotype when treated at heights of 10, 20, and 30 cm, respectively. Sequence analysis of the EPSPS gene revealed no point mutations at the Pro106 and Thr102 residues in the CT-Res Palmer amaranth biotype. Quantitative polymerase chain reaction analysis revealed that the CT-Res biotype had 33 to 111 relative copies of the EPSPS gene compared with the AL-Sus biotype. All these results suggest that the EPSPS gene amplification endows a high level of glyphosate resistance in the GR Palmer amaranth biotype from Connecticut. Because of the lack of control with glyphosate, growers should adopt the use of effective alternative preemergence and postemergence herbicides in conjunction with other cultural and mechanical tactics to mitigate the further spread of GR Palmer amaranth in Connecticut.

Response characterization and target site mechanism study in glyphosate-resistant populations of Lolium multiflorum L. from Brazil

Italian ryegrass (Lolium multiflorum L.) is an invasive species widely spread in croplands worldwide. The intensive use of glyphosate has resulted in the selection of resistance to this herbicide in Italian ryegrass. This work characterized the response to glyphosate of Italian ryegrass populations from the South and Southwest regions of Paraná, Brazil. A total of 44 Italian ryegrass populations were collected in farming areas, and were classified for glyphosate resistance with 75% of populations resistant to gloyphosate. Of these, 3 resistant (VT05AR, MR20AR and RN01AR) and three susceptible (VT07AS, MR05AS and RN01AS) of these populations were selected to determine the resistance level and the involvement of the target site mechanisms for glyphosate resistance. Susceptible populations GR50 ranged from 165.66 to 218.17 g.e.a. ha−1 and resistant populations from 569.37 to 925.94, providing RI ranging from 2.88 and 4.70. No mutation in EPSPS was observed in the populations, however, in two (MR20AR and RN02AR) of the three resistant populations, an increase in the number of copies of the EPSPs gene (11 to 57×) was detected. The number of copies showed a positive correlation with the gene expression (R2 = 0.86) and with the GR50 of the populations (R2 = 0.81). The increase in EPSPS gene copies contributes to glyphosate resistance in Italian ryegrass populations from Brazil.

EPSPS regulates cell elongation by disrupting the balance of lignin and flavonoid biosynthesis in cotton

EPSPS is a key gene in the shikimic acid synthesis pathway that has been widely used in breeding crops with herbicide resistance. However, its role in regulating cell elongation is poorly understood. Through the overexpression of EPSPS genes, we generated lines resistant to glyphosate that exhibit an unexpected dwarf phenotype. A representative line, DHR1, exhibits a stable dwarf phenotype throughout its entire growth period. Except for plant height, the other agronomic traits of DHR1 are similar to its transgenic explants ZM24. Paraffin section observations showed that DHR1 internodes are shortened due to reduced elongation and division of the internode cells. Exogenous hormones confirmed that DHR1 is not a classical brassinolide (BR)- or gibberellin (GA)-related dwarfing mutant. Hybridization analysis and fine mapping confirmed that the EPSPS gene is the causal gene for dwarfism, and the phenotype can be inherited in different genotypes. Transcriptome and metabolome analyses showed that genes associated with the phenylpropanoid synthesis pathway are enriched in DHR1 compared with ZM24. Flavonoid metabolites are enriched in DHR1, whereas lignin metabolites are reduced. The enhancement of flavonoids likely results in differential expression of auxin signal pathway genes and alters the auxin response, subsequently affecting cell elongation. This study provides a new strategy for generating dwarfs and will accelerate advancements in light simplification in the cultivation and mechanized harvesting of cotton.

Identification and Expression Analysis of EPSPS and BAR Families in Cotton.

Weeds seriously affect the yield and quality of crops. Because manual weeding is time-consuming and laborious, the use of herbicides becomes an effective way to solve the harm caused by weeds in fields. Both 5-enolpyruvyl shikimate-3-phosphate synthetase (EPSPS) and acetyltransferase genes (bialaphos resistance, BAR) are widely used to improve crop resistance to herbicides. However, cotton, as the most important natural fiber crop, is not tolerant to herbicides in China, and the EPSPS and BAR family genes have not yet been characterized in cotton. Therefore, we explore the genes of these two families to provide candidate genes for the study of herbicide resistance mechanisms. In this study, 8, 8, 4, and 5 EPSPS genes and 6, 6, 5, and 5 BAR genes were identified in allotetraploid Gossypium hirsutum and Gossypium barbadense, diploid Gossypium arboreum and Gossypium raimondii, respectively. Members of the EPSPS and BAR families were classified into three subgroups based on the distribution of phylogenetic trees, conserved motifs, and gene structures. In addition, the promoter sequences of EPSPS and BAR family members included growth and development, stress, and hormone-related cis-elements. Based on the expression analysis, the family members showed tissue-specific expression and differed significantly in response to abiotic stresses. Finally, qRT-PCR analysis revealed that the expression levels of GhEPSPS3, GhEPSPS4, and GhBAR1 were significantly upregulated after exogenous spraying of herbicides. Overall, we characterized the EPSPS and BAR gene families of cotton at the genome-wide level, which will provide a basis for further studying the functions of EPSPS and BAR genes during growth and development and herbicide stress.

Divergence in Glyphosate Susceptibility between Steinchisma laxum Populations Involves a Pro106Ser Mutation.

The characterization of the mechanisms conferring resistance to herbicides in weeds is essential for developing effective management programs. This study was focused on characterizing the resistance level and the main mechanisms that confer resistance to glyphosate in a resistant (R) Steinchisma laxum population collected in a Colombian rice field in 2020. The R population exhibited 11.2 times higher resistance compared to a susceptible (S) population. Non-target site resistance (NTSR) mechanisms that reduced absorption and impaired translocation and glyphosate metabolism were not involved in the resistance to glyphosate in the R population. Evaluating the target site resistance mechanisms by means of enzymatic activity assays and EPSPS (5-enolpyruvylshikimate-3-phosphate synthase) gene sequencing, the mutation Pro106Ser was found in R plants of S. laxum. These findings are crucial for managing the spread of S. laxum resistance in Colombia. To effectively control S. laxum in the future, it is imperative that farmers use herbicides with different mechanisms of action in addition to glyphosate and adopt Integrate Management Programs to control weeds in rice fields of the central valleys of Colombia.

In maize, co-expression of GAT and GR79-EPSPS provides high glyphosate resistance, along with low glyphosate residues

Herbicide tolerance has been the dominant trait introduced during the global commercialization of genetically modified (GM) crops. Herbicide-tolerant crops, especially glyphosate-resistant crops, offer great advantages for weed management; however, despite these benefits, glyphosate-resistant maize (Zea mays L.) has not yet been commercially deployed in China. To develop a new bio-breeding resource for glyphosate-resistant maize, we introduced a codon-optimized glyphosate N-acetyltransferase gene, gat, and the enolpyruvyl-shikimate-3-phosphate synthase gene, gr79-epsps, into the maize variety B104. We selected a genetically stable high glyphosate resistance (GR) transgenic event, designated GG2, from the transgenic maize population through screening with high doses of glyphosate. A molecular analysis demonstrated that single copy of gat and gr79-epsps were integrated into the maize genome, and these two genes were stably transcribed and translated. Field trials showed that the transgenic event GG2 could tolerate 9000 g acid equivalent (a.e.) glyphosate per ha with no effect on phenotype or yield. A gas chromatography-mass spectrometry (GC–MS) analysis revealed that, shortly after glyphosate application, the glyphosate (PMG) and aminomethylphosphonic acid (AMPA) residues in GG2 leaves decreased by more than 90% compared to their levels in HGK60 transgenic plants, which only harbored the epsps gene. Additionally, PMG and its metabolic residues (AMPA and N-acetyl-PMG) were not detected in the silage or seeds of GG2, even when far more than the recommended agricultural dose of glyphosate was applied. The co-expression of gat and gr79-epsps, therefore, confers GG2 with high GR and a low risk of herbicide residue accumulation, making this germplasm a valuable GR event in herbicide-tolerant maize breeding.

Co-expression of multi-gene in cotton promotes the aggregation of multi-resistance and yield traits

Given the diminishing availability of cultivable lands and environmental degration, it has become imperative to develop cotton varieties that possess resistance against diverse abiotic and biotic stresses, and improved yields. However, conventional breeding techniques such as crossbreeding has proven to be inefficient and time-consuming for generating novel varieties. Transgenic breeding technology offers advantages such as shortened breeding cycle, overcoming reproductive isolation, and precise integration of single or multiple genes into host plants. In this study, we incorporated six genes including the apoptosis inhibitors p35 and IAP, high yield related gene Bn-cs RRM2, drought resistance gene HDG11, glyphosate resistance gene EPSPS, and insect resistance gene Cry1AC into the pBI121 vector, which was then transformed into cotton plants via Agrobacterium-mediated transformation. The overexpression of these genes significantly enhanced plant tolerance to Verticillium wilt, drought, glyphosate, and cotton bollworm, along with high yields in field conditions. Our results suggested that the integration of multiple genes in cotton is a potential strategy for breeding cotton varieties with broad resistance traits.

Confirmation of a five‐way herbicide‐resistant Amaranthus tuberculatus population in North Carolina

AbstractAmaranthus tuberculatus (waterhemp) is a pervasive weed of the Mid‐west and ‐south United States and is not native to North Carolina but infestations in crop fields have been reported recently. Amaranthus tuberculatus has evolved resistance to seven herbicide groups and multiple herbicide‐resistant populations are common where the species is native. The reported A. tuberculatus infestations in North Carolina have not been controlled with herbicides but no formal herbicide resistance characterisation has been conducted to date. Glasshouse dose–response experiments were conducted to determine the susceptibility of a population collected from Surry County, North Carolina to commonly applied postemergence herbicides compared to a herbicide‐susceptible population collected from Story County, Iowa. The Surry County population survived labelled rates of imazethapyr, atrazine, glyphosate, fomesafen, and mesotrione; the Story County population was controlled with these herbicides. Further, 2,4‐D, dicamba, and glufosinate effectively controlled the Surry and Story County populations. Molecular sequencing assays were subsequently conducted to determine if altered target sites facilitated resistance in the acetolactate synthase (ALS), 5‐enolpyruvylshikimate‐3‐phosphate synthase (EPSPS), photosystem II (psbA), and protoporphyrinogen oxidase (PPX2) genes. The Surry County population carried a Trp574Leu and ∆Gly210 mutations in the ALS and PPX2 gene, respectively. No mutations that would confer resistance were found in the EPSPS or psbA gene for either population. The results of both experiments provide evidence that a five‐way herbicide‐resistant A. tuberculatus population has encroached North Carolina. More research is needed to determine the mechanisms of resistance to atrazine, glyphosate, and mesotrione.

Extrachromosomal DNA-mediated glyphosate resistance in Italian ryegrass.

An Italian ryegrass population from Arkansas, USA developed glyphosate resistance due to 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) gene amplification. The plants in this population with approximately 70 EPSPS copies were used in the present study for the physical mapping of amplified copies of EPSPS gene to determine the possible mechanism of EPSPS gene amplification conferring glyphosate resistance in Italian ryegrass. Fluorescence in situ hybridization (FISH) analysis of glyphosate resistant (GR) Italian ryegrass plants with approximately 70 EPSPS copies displayed EPSPS hybridization signals randomly on most of the metaphase chromosomes. Glyphosate susceptible (GS) Italian ryegrass plants with one EPSPS copy displayed single prominent EPSPS hybridization signal, which was co-localized with 5S rDNA locus along with few additional signals on the outside of chromosomes. Pulsed-field gel electrophoresis (PFGE) followed by DNA blot using EPSPS gene as a probe identified a prominent EPSPS hybridization around the 400 kb region in GR DNA samples, but not in GS DNA samples. We report the extrachromosomal DNA-mediated glyphosate resistance in Italian ryegrass. Physical mapping of amplified copies of EPSPS gene in Italian ryegrass by FISH gives us a clue that the amplified copies of EPSPS gene may be present in the extrachromosomal DNA elements. Further analysis by PFGE followed by DNA blotting revealed that the extrachromosomal DNA containing EPSPS is approximately 400 kb similar in size with that of eccDNA replicon in Amaranthus palmeri. © 2023 Society of Chemical Industry.