2023
DOI: 10.1186/s13059-023-02950-9
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Genome-wide association analysis reveals a novel pathway mediated by a dual-TIR domain protein for pathogen resistance in cotton

Abstract: Background Verticillium wilt is one of the most devasting diseases for many plants, leading to global economic loss. Cotton is known to be vulnerable to its fungal pathogen, Verticillium dahliae, yet the related genetic mechanism remains unknown. Results By genome-wide association studies of 419 accessions of the upland cotton, Gossypium hirsutum, we identify ten loci that are associated with resistance against Verticillium wilt. Among these loci, … Show more

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Cited by 14 publications
(3 citation statements)
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References 86 publications
(110 reference statements)
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“…tomato ( Pst ) DC3000. V. dahliae is a soil‐borne fungal pathogen responsible for severe losses of biomass, yield and quality in plenty of economically important crops including tomato and cotton (Zhang et al ., 2023 ), while P. syringae represents a model biotrophic bacterial pathogen that has been extensively investigated in tomato and Arabidopsis (Xin and He, 2013 ). Three‐week‐old tomato seedlings of wild‐type and sldml2 mutants that display non‐differential stem lengths were inoculated with V. dahliae and the disease response was observed at 18 days post‐inoculation (dpi) (Figure S5a,b ).…”
Section: Resultsmentioning
confidence: 99%
“…tomato ( Pst ) DC3000. V. dahliae is a soil‐borne fungal pathogen responsible for severe losses of biomass, yield and quality in plenty of economically important crops including tomato and cotton (Zhang et al ., 2023 ), while P. syringae represents a model biotrophic bacterial pathogen that has been extensively investigated in tomato and Arabidopsis (Xin and He, 2013 ). Three‐week‐old tomato seedlings of wild‐type and sldml2 mutants that display non‐differential stem lengths were inoculated with V. dahliae and the disease response was observed at 18 days post‐inoculation (dpi) (Figure S5a,b ).…”
Section: Resultsmentioning
confidence: 99%
“…cDNAs were synthesized using the PrimeScript RT reagent kit with gDNA Eraser (Takara). Reverse transcriptase quantitative PCR (RT‐qPCR) was performed using the SuperReal PreMix Plus Kit (Tiangen), with the following amplification parameters: 94 °C for 5 min, followed by 27 cycles of 98 °C for 15 s, 60 °C for 15 s, and 68 °C for 30 s. The detailed quantitative reverse transcriptase PCR analysis refers to our previous research (Zhang et al ., 2023 ). The gene‐specific primers used for RT‐qPCR were designed using the Primer Database (Lu et al ., 2018 ), which were listed in Table S4 .…”
Section: Methodsmentioning
confidence: 99%
“…GWASs are an effective strategy for uncovering the genetic architecture of complex traits by associating genetic variations with phenotypic variations at the population level [13][14][15]. Over the last decade, many genetic loci/genes have been identified by using this approach in rice [16], maize [17,18], wheat [19], soybean [20], cotton [21], tomato [22], melon [23], watermelon [24], etc. Thus, GWASs have been widely used to study important traits that are related to plant genetics and breeding, thus effectively promoting germplasm innovation and molecular breeding.…”
Section: Introductionmentioning
confidence: 99%