Abstract
Verticillium wilt (VW) is a soil-borne fungal disease that is caused by Verticillium dahliae Kleb and seriously damages cotton production annually in China. To date, many efforts have been made to improve the resistance of upland cotton against VW, but little progress has been achieved because of a lack of resistant upland cotton to VW. G. barbadense is known to carry high resistance to VW; however, it is difficult to transfer the resistance trait from G. barbadense to upland cotton because of linkage drag and distortion in the interspecific hybrid. In this study, a chromosomal segment introgression line (CSIL), SuVR043, containing a single and homozygous chromosome segment of G. barbadense cv. H7124 D04 (Chr 22), was created and used to construct an F2 population for mapping of VW resistance quantitative trait loci (QTLs) in the greenhouse. Two major resistance QTLs against nondefoliating V. dahliae isolate Bp2, called qVW-Bp2-1 and qVW-Bp2-2, which were flanked by the markers cgr6409-ZHX37 and ZHX57-ZHX70 and explained an average of 16.38 and 22.36% of the observed phenotypic variation, respectively, were detected in three independent replicate experiments. The genetic distances from cgr6409 to ZHX37 and from ZHX57 to ZHX70 were 2.4 and 0.8 cM, respectively. By analyzing the genome sequence of the qVW-Bp2-1 and qVW-Bp2-2 regions, we determined that the accurate physical distances from cgr6409 to ZHX37 and from ZHX57 to ZHX70 in the G. barbadense genome are 254 and 140 kb, and that those spans 36 and 20 putative genes, respectively. The results of the expression analysis showed significant differences in the expression profiles of GbCYP450, GbTMEM214, and GbRLK among G. barbadense cv. H7124, CSIL SuVR043 and G. hirsutum acc. Sumian 8 at different times after inoculation with V. dahliae isolate Bp2. Virus-induced gene silencing (VIGS) analysis showed that silencing of GbCYP450 and GbTMEM214 decreased H7124 and CSIL SuVR043 resistance to VW. These results form a solid foundation for fine mapping and cloning of resistance genes in the substituted segment and will provide valuable assistance in future efforts to breed for VW resistance.
Highlights
Cotton (Gossypium spp.) is widely cultivated for the important economic value of its fiber
470 simple sequence repeat (SSR) markers that were approximately evenly spaced across the cotton genome based on G. hirsutum × G. barbadense maps were used to analyze the foreground and background of chromosomal segment introgression line (CSIL) SuVR043 (Zhao et al, 2012), and this study detected one SSR marker (NAU3392) that was polymorphic between G. hirsutum cv
We used 3100 SSR markers to further select the background of CSIL SuVR043, of which 1,750 markers were mapped and distributed on 26 cotton chromosomes based on the published genetic map of G. hirsutum × G. barbadense (Zhao et al, 2012), and identified four makers (NAU3392, NAU3791, NAU5294, and JESPR220) to be polymorphic between CSIL SuVR043 and Sumian 8
Summary
Cotton (Gossypium spp.) is widely cultivated for the important economic value of its fiber. A great deal of research in comparative genomics has revealed that the V. dahliae can degrade plant cell walls by the expansion of some CAZyme families, and that flexible genomic islands containing TE and LS genes contribute to the development of virulence and host adaptation by the De et al (2013). In China, V. dahliae strains that have cotton as their main host are divided into defoliating and nondefoliating strains. The main differences between them are that the defoliating strains develop into epidemics earlier and more rapidly and cause significantly greater yield losses than the nondefoliating strains at equal inoculum densities (BejaranoAlcazar et al, 1995). Breeding and planting resistant varieties to VW is the most effective and economical method to control the epidemic. The fine mapping and cloning of resistant genes will be the key to achieve this goal
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
