A breeding method for high-yield, disease-resistant and strong-gluten wheat in the middle and lower reaches of the Yangtze River
A high-yield, disease-resistant, mid- and downstream technology, applied in the fields of botanical equipment and methods, biochemical equipment and methods, and plant genetic improvement, can solve the problems of long breeding cycle, stability, and large separation of progeny traits, and accelerate the breeding process. , Shorten the breeding years, the effect of comprehensive disease resistance is good
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Embodiment 1
[0047] Embodiment 1, a kind of high-yield, disease-resistant and strong-gluten wheat breeding method in the middle and lower reaches of the Yangtze River
[0048] Parental selection: Most of the main cultivars with excellent comprehensive agronomic traits and good comprehensive disease resistance and their derived cultivars (lines) in the middle and lower reaches of the Yangtze River were screened for the scab resistance locus QFhs.crc-2DL. As a positive control, Yangmai 17 was screened as parent 1.
[0049] 1) Planted in January 2006, and from April to May, the wheat variety Yangmai 17 carrying the scab resistant locus QFhs.crc-2DL in the middle and lower reaches of the Yangtze River was used as the male parent, and the intermediate material "Amigo" resistant to powdery mildew was selected As the female parent, hybridize in the greenhouse and harvest the hybrid F1 at the end of June;
[0050] Amig is a powdery mildew resistant strain (References: Zhang Xu, Zang Yuhui, Liu Zh...
Embodiment 2
[0065] Example 2. Establishment of Molecular Markers to Detect the Anti-Gibberella Disease Site QFhs.crc-2DL Method
[0066] The primer set of molecular marker Xgwm539 was used to detect whether Yangmai 17, leaves of F3 single plant, and mixed leaves of F4 lines carried the resistance genotype QFhs.crc-2DL.
[0067] 1. The genomic DNA of Yangmai 17, F3 individual leaves, and F4 mixed leaves were extracted by CTAB method, and the template solution with DNA concentration of about 30ng / μL was obtained by dilution.
[0068] 2. Using the genomic DNA extracted in step 1 as a template, PCR amplification was carried out using Xgwm539, an anti-head blight marker for detecting wheat as described in Example 1, to obtain an amplification product.
[0069] The primer sequences used in this study to identify the scab-resistant locus QFhs.crc-2DL are shown in Table 2:
[0070] Table 2 QFhb-YM17 linked marker primer sequence information
[0071]
[0072] A PCR amplification method was us...
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