Special primer for identifying which variety of Glu-A3 protein subunit is carried in wheat as well as application thereof
A wheat and protein technology, applied in application, plant genetic improvement, recombinant DNA technology, etc., can solve the problems of limiting the analysis and utilization of LMW-GS, lack of simple and effective identification methods, etc., to speed up the breeding speed and reduce the breeding cost. , optimize the effect of hybrid combination
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Embodiment 1
[0034] Example 1. Obtaining the Glu-A3 Site Gene of Common Wheat Low Molecular Weight Glutenin
[0035] The wheat varieties used are listed in Table 1.
[0036] Table 1 Wheat varieties used for cloning Glu-A3 locus genes and analyzing Glu-A3 subunit-specific markers
[0037]
[0038] The seven wheat varieties in Table 1 are all wheat containing the identified Glu-A3 protein subunit (Vawser MJ, Cornish GB, Shepherd KW (2002) Rheological dough properties of Aroonisolines differing in glutenin subunit composition.In: Cereals 2002, Proceedings of the 52nd Australian Cereal Chemistry Conference. Christchurch, New Zealand. (Eds CK Black, JF Panozzo, CW Wrigley, IL Batey and N Larsen) pp.53-58. (Cereal Chemistry Division, Royal Australian Chemical Institute)).
[0039] According to the Glu-A3 site related sequence on GenBank (GENBANK ACCESSION NO.EU189087, AB062868, FJ441117 and EF426565), design 3 pairs of primers as follows:
[0040] Primer pair A: P1 (upstream primer): 5'-AAA...
Embodiment 2
[0054] Example 2. Obtainment of Glu-A3 Subunit Specific Marker of Common Wheat Low Molecular Weight Glutenin
[0055] According to the corresponding relationship between the 3 Glu-A3 genes and Glu-A3 protein subunits obtained above, after sequence alignment, 7 pairs of specific primer pairs for recognizing Glu-A3 protein subunits were designed according to the differences between gene allelic variations , see Table 2.
[0056] Table 2 Specific primer pairs for identifying Glu-A3 protein subunits
[0057]
[0058] The genomic DNA of wheat in Table 1 was amplified by PCR using the above 7 pairs of primers respectively.
[0059] The PCR reaction system was as follows: 50 ng of template DNA, 1 U of Taq enzyme (TaKaRa), upstream and downstream primers (5 μmol L -1 ) each 1.2μl, dNTP (2.5mmol·L -1 , TaKaRa) 0.8 μl, 10×PCR buffer 2 μl, supplement the reaction system with sterile distilled water to 20 μl.
[0060] PCR reaction program: 94°C for 5min; then 94°C for 35s, 60°C for...
Embodiment 3、 7
[0063] Embodiment 3, application and result verification of seven pairs of specific primer pairs
[0064] In order to further verify the practicability of 7 pairs of specific primer pairs developed, 7 pairs of primers were used to detect 121 wheat materials (numbering 8-128) and 7 materials (numbering 1-7) used for cloning genes in Example 1, The results are shown in Table 3. The Glu-A3 site protein subunits of these materials have been analyzed by SDS-PAGE, so the detection results of 7 pairs of specific primer pairs can be verified. Figure 8 The Glu-A3, Glu-B3 and Glu-D3 subunit results of some materials were detected for SDS-PAGE. Figure 8 Medium, 1:21; 2:26; 3:30; 4: Pavón (control); 5:8; 6:11; 7:17; 8:19; 9:31; 10:90; 11:18; 12 : 24; 13: 25; 14: Opata (control); the above numbers refer to the numbers in Table 3. The control is to provide a reference position of the corresponding band.
[0065] Table 3 Verification of Glu-A3 protein subunit-specific STS labeling
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