A Molecular Marker Tightly Linked to the Qtl Locus of Kiwi Fruit Weight Traits and Its Application
A technology of kiwifruit and kiwifruit, which is applied in the fields of molecular biology and genetic breeding, can solve the problems that molecular marker research has not yet been carried out, and achieve the effects of convenient and fast detection methods, saving production costs, and improving selection efficiency
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Embodiment 1
[0022] Acquisition of molecular markers linked to main effect QTL and development of kiwifruit fruit weight:
[0023] ① In this example, the kiwifruit 'MT570001' with a small fruit weight and the Chinese kiwifruit 'Guihai No. 4' with a large fruit weight were used to construct F 1 Separate groups. In the 6th year of fruiting of the population, select 150 F 1 The individual plants of the offspring of the population were the research objects.
[0024] ②A total of 150 individual plant leaves were collected from the population, and the total DNA was extracted by the CTAB method. According to the RADseq method, the libraries of Chinese kiwifruit 'Guihai 4', Shanli kiwifruit 'MT570001' and 150 offspring were constructed and sequenced.
[0025] ③ Filter the sequencing data to remove sequences with low-quality base content greater than 50%, and remove sequences with sequencing adapter contamination and a large number of repetitions. Use the software SOAP2 to compare the sequencing...
Embodiment 2
[0035] The application of a molecular marker closely linked to the QTL locus of kiwi fruit weight traits in kiwi fruit breeding, the steps are:
[0036] (1) F 1 Generation, select F 1 60 individual plants in the generation population were the research objects.
[0037] (2) At the ripening stage of the fruit, collect F 1 The fruit of 60 individual plants in the generation group, 40 fruits were collected from each plant, and the weight of the fruit was measured with a weighing balance to calculate the average fruit weight.
[0038] (3) Extract F 1 Generation of total DNA of 60 individual plants, according to Premix Ex Taq TM II (Tli RNaseHPlus), ROX plus kit instruction, design 20uL reaction system: 5ng·uL -1 Kiwifruit genomic DNA template 2ul, 2×SYBR Premix 10ul, 50×ROX Dye II 0.4ul, 10uM FW-F and FW-R each 0.8ul, double distilled water to make up the rest. The amplification program was: pre-denaturation at 95°C for 5 s, annealing at 60°C for 1 min; denaturation at 95°C...
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