A kind of maize waxy gene mutant and its molecular marker and application
A technology of molecular markers and protein mutants, applied in the fields of application, genetic engineering, plant gene improvement, etc., can solve problems such as easy loss, and achieve the effects of convenient material collection, increased amylopectin content, and shortened identification and breeding processes
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Embodiment 1
[0041] The following examples are used to illustrate the present invention, but are not intended to limit the scope of the present invention. Example 1 Obtaining of maize waxy gene mutant wx-hAT
[0042] 200 germplasms of waxy maize inbred lines were collected from the maize germplasm resource bank of the Maize Research Center of Beijing Academy of Agriculture and Forestry Sciences, and the DNA of maize leaves was extracted using the plant DNA extraction kit of TianGen Company. The segment from exon 1 to exon 14 was amplified. Sequencing analysis revealed that among 200 germplasms of waxy maize inbred lines, 8 maize materials carried a new allelic mutation of the waxy gene. The first exon to the fourth exon of the waxy gene of these eight materials were amplified by PCR with E1-4F / R primers. PCR amplification conditions were: 94°C, 5min, then 94°C, 60s, 59°C, 60s, 72°C, 2min for 34 cycles, and finally 72°C extension for 10min. Electrophoresis detection found that the size of...
Embodiment 2
[0051] Example 2 cDNA sequence analysis of maize waxy gene mutant wx-hAT
[0052] The wx-hAT type waxy maize leaf RNA obtained in Example 1 was extracted by the Trizol method, and the RNA was reverse-transcribed into cDNA by a reverse transcription kit (Takara). The cDNA sequences were amplified with waxycDNAF2 and WaxycDNAR2 primers (Table 4). The PCR amplification conditions were: 94°C for 5min, then 38 cycles of 94°C, 60s, 56°C, 60s, 72°C, 2min, and finally 72°C for 10min. Electrophoresis detection found that the size of the amplified fragment in the common maize inbred line B73 was 163bp, while the amplified fragment in the wx-hAT type waxy maize HN2 was 1342bp ( figure 2 ). Sequencing analysis found that 1179 bp of the 2.2 kb insert was exonized in wx-hAT type waxy maize ( image 3 ), the exonized sequence contains a stop codon, resulting in premature termination of translation of the inserted protein. This result further confirms that the loss of function of the wax...
Embodiment 3
[0055] Example 3 Development and Application of Specific Functional Molecular Markers of Maize Waxy Gene Mutant wx-hAT
[0056] Based on the sequence difference between wx-hAT waxy maize and common maize in the third exon of the waxy gene, a site-specific PCR functional molecular marker PCR-hAT was developed. The amplification primer information of this molecular marker is shown in Table 5.
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