dcaps molecular markers for identification of rice ear length traits and their applications
A molecular marker, rice technology, applied in the field of molecular biology, can solve the problem of low probability of discrimination and recognition
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Embodiment 1
[0037] Example 1 is used to identify the development of dCAPS molecular markers of rice panicle length traits
[0038] 1. Mining SNP loci significantly associated with rice long panicle traits by SLAF-Seq method
[0039] (1) Select two rice cultivars from different sources and have significant differences in panicle length traits to construct a population of recombinant inbred lines (RILs) by crossing G1025 (short panicle) and K1561 (long panicle);
[0040] (2) Using the specific site amplified fragment (SLAF) sequencing technology, a high-density genetic linkage map was constructed using the genotype data of the RILs population;
[0041] (3) Based on the genetic linkage map, the quantitative trait loci (QTL) of panicle length in the RILs population were analyzed, and a main effect QTL (called PL9) controlling panicle length was detected, and obtained the long panicle of rice. SNP loci significantly associated with traits;
[0042] 2. SNP site-specific restriction enzyme sit...
Embodiment 2
[0052] Example 2 Verification of dCAPS molecular markers for identifying rice panicle length traits
[0053] (1) Genomic DNA of 12 short-eared rice varieties and 12 long-eared rice varieties was extracted by CTAB method. After detecting the concentration and purity of DNA with a nucleic acid analyzer, the ddH 2 O is diluted to 300ng / L for subsequent use;
[0054] (2) Use the specific primer pairs designed in Example 1 to perform PCR amplification on 24 materials. The 20 μL PCR amplification reaction system is: 1 μL of genomic DNA to be tested, 0.5 μL of upstream and downstream primers, 10 μL of 2×Es Taq DNA Polymerase Reactionmix (TIANGEN, Beijing), 8 μL of distilled water. The PCR amplification reaction program is: denaturation at 94°C for 5 minutes; 30 cycles at 94°C for 30s, 57°C for 30s, and 72°C for 30s; extension at 72°C for 5 minutes;
[0055] (3) After the PCR reaction, 10 μL of the reaction product was detected by 2% agarose gel electrophoresis, and a single band wa...
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