Earliness gene eam.z as well as molecular marker SNP595 and application thereof
A technology of molecular markers and genes, which is applied in the field of molecular biology, can solve problems such as prominent stubble gaps, multiple cropping, and short harvest intervals in multi-cropping systems, and achieve the effect of improving selection efficiency and speeding up the progress
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Embodiment 1
[0032] Example 1 Molecular marker SNP595
[0033] 1) The present invention uses the chemical mutagen EMS to treat the barley variety Hua 30, and obtains an early-maturing mutant Zhezaomai No. 1 with stable traits through multiple generations of screening and identification, and clones the early-maturing gene eam.z by gene mapping and other methods, and studies It was found that the base of the eam.z gene at 595bp in the coding region of the wild-type barley gene HORVU3Hr1G114970 changed from A to T, forming a stop codon TAG, which led to the premature termination of the encoded protein and a premature phenotype. The point is different from the previously reported barley early maturity gene mutation site ( figure 1 ). Utilizing the mutation site, the present invention designs a KASPar marker, which can quickly and accurately detect whether the barley material contains the eam.z mutation gene.
[0034] The phenotype of the early-maturing mutant Zhezaomai 1 was as follows: the...
Embodiment 2
[0044] Example 2 Molecular marker identification eam.z genotype
[0045] Methods for identifying eam.z genotypes using molecular markers:
[0046] 1) DNA extraction: Take 100 mg of barley leaves, and use the CTAB method to extract DNA. The specific steps are as follows:
[0047]① Grind the sheared leaves in liquid nitrogen and put them into 1.5ml centrifuge tubes, add 600 μL of CTAB to each tube and place in a warm water bath at 65°C for 50-60 minutes (take out every 10 minutes and shake gently);
[0048] ②Add 600 microliters of chloroform / isoamyl alcohol (24:1) and mix well for 15 minutes. Slowly, weigh in pairs, and after balancing, centrifuge at 9600 rpm for 10 minutes at 4°C;
[0049] ③Pipe the supernatant to another 1.5ml new centrifuge tube, add 2 times the volume of absolute ethanol and mix slightly (precipitate in -20°C refrigerator for 30-60min);
[0050] ④ Pick out the precipitate with a pipette tip, put it in a 1.5ml centrifuge tube, wash it twice with 70% ethanol...
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