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Method for identifying silkworm silk color in larval stage

A technology for larval stage and silkworm, which is applied in the field of identifying silkworm spinning color in the larval stage, can solve the problems of unidentifiable, difficult to stabilize cocoon color of selected strains, and inability to simultaneously identify genotypes and preserve seeds.

Inactive Publication Date: 2012-12-05
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] At present, domestic and foreign silkworm colored cocoon breeding methods are based on cocoon color evaluation and selection of families and individuals. However, due to the aforementioned yellow and red cocoon colors, homozygous and heterozygous families cannot be judged. Consistency and high color fastness The selection of families and individuals can only be achieved through cocoon color measurement and cocoon silk color fastness testing, resulting in a lack of accuracy in the selection of silkworm varieties with yellow and red cocoons, and it is difficult to breed strains Stable cocoon color, long breeding cycle, high cost and poor effect
Although theoretically by examining the mRNA structure of the Cbp gene and Cbp-like gene transcription, or detecting the CBP protein product, the carotenoid-binding protein genotype of the individual can be confirmed, but the Cbp gene and Cbp-like gene of the silkworm are mainly found in the 5th instar larvae. Silk gland and digestive tract transcription and expression, identification of Cbp gene and Cbp-like gene transcription and expression product types need to kill larvae to take out silk gland or digestive tract tissue, it is impossible to achieve both identification of gene type and seed retention, and it is also impossible to extract from silkworm cocoons The identification and separation of the mixed populations of yellow-red cocoon systems with different cocoon layer colors and different chromaticity can not meet the needs of natural color cocoon variety breeding.

Method used

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  • Method for identifying silkworm silk color in larval stage
  • Method for identifying silkworm silk color in larval stage

Examples

Experimental program
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Effect test

Embodiment 1

[0026] In order to identify the green cocoon Dazao variety with yellow-green cocoon color, the white cocoon variety C108 with pure white cocoon color, the yellow cocoon system Caicoon No. YO, this embodiment has carried out the following steps:

[0027] (1) The total RNA of the silk glands of the above four 5th instar larval samples was extracted with a commercial RNA extraction kit (Qiagen), and cDNA was synthesized by reverse transcription, and stored at -20°C to -40°C until use. For reverse transcription, use the reverse transcription kit from TaKaRa Company, reverse transcription reaction system (10 μL): 5×PrimeScript TM Buffer 2μL; PrimeScript TM EnzymeMixI 0.5μL; 50μmol / L Oligo dT Prime (50μmol / L) 0.5μL; Total RNA 1μL; add RNase FreeH 2 O to a total volume of 10 μL. The reverse transcription conditions were: 37°C for 15 minutes; 85°C for 5s.

[0028] (2) Using the four silkworm cDNAs obtained in step (1) as templates, using an upstream primer having a nucleotide se...

Embodiment 2

[0041] From the mixed populations with different cocoon layer colors and different chromaticity, the families with consistent cocoon color inside and outside and high color fastness were isolated.

[0042] (1) Raise in a single moth area, take a certain number of larval samples from each of the 100 moth areas at the 5th instar, and extract the total RNA from each larval silk gland according to the method described in Example 1, according to the embodiment cDNA was synthesized by the reverse transcription method described in 1, and stored at -20°C to -40°C for future use.

[0043] (2) Using the silk gland cDNA of Bombyx mori extracted in step (1) as a template, use the upstream primer with the nucleotide sequence shown in SEQ ID NO: 1 and the primer with the nucleotide sequence shown in SEQ ID NO: 2 For downstream primers, the Actin 3 gene was used as an internal reference gene, and RT-PCR was amplified according to the method described in Example 1.

[0044] (3) The RT-PCR am...

Embodiment 3

[0053] The homozygous yellow silk-spitting silkworm was selected from the mating of the homozygous yellow silk-spitting silkworm and the white cocoon excellent variety.

[0054] (1) The pure line Y12 of silkworm yellow cocoon was crossed with JS silkworm variety JS, which has a large amount of silk, high silk quality, and strong resistance. The blood of all larvae is all yellow 100 moth districts to get a certain number of larvae samples, and the total RNA extracted from each larvae silk gland according to the method described in Example 1 is reverse transcribed according to the method described in Example 1. Methods cDNA was synthesized and stored at -20°C to -40°C for future use.

[0055] (2) Using the silk gland cDNA of Bombyx mori extracted in step (1) as a template, use the upstream primer with the nucleotide sequence shown in SEQ ID NO: 1 and the primer with the nucleotide sequence shown in SEQ ID NO: 2 For downstream primers, the Actin 3 gene was used as an internal re...

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Abstract

The invention belongs to the field of biotechnology, and discloses a method for identifying a silkworm silk color in a larval stage. The method provided by the invention comprises the following steps of: extracting the ribonucleic acid (RNA) of a silkworm silk gland of a 5th instar stage to be detected by utilizing a genetic engineering technology; performing reverse transcription to synthesize complementary deoxyribonucleic acid (cDNA); taking the obtained cDNA as a template, performing reverse transcription-polymerase chain reaction (RT-PCR) amplification reaction by using a specific primer; judging whether a silkworm spins yellow silk or green silk or white silk by detecting the type and the length of a PCR amplification product by agarose electrophoresis; and further judging whether the silkworm which spins the yellow silk is a homozygous yellow silk spinning silkworm or a heterozygous yellow silk spinning silkworm, and other silkworms spin green silk or white silk by analyzing the content of the RT-PCR amplification product relative to an electrophoresis gel product. By the method provided by the invention, the pedigree with consistent internal cocoon color and external cocoon color and high color fastness also can be identified and separated from a mixed group with different cocoon layer colors and chromaticities. The identification method provided by the invention is simple, convenient and rapid to operate; and the accuracy for identifying the color of the silkworms is high.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a method for identifying the silk color of silkworm silkworm, specifically using the specific sequence of mRNA transcribed from the Cbp gene and the Cbp-like gene of silkworm, to specifically identify the silk silk color of silkworm, and at the same time distinguish the silkworm silk The silkworm with yellow silk and the silkworm with part of yellow silk, the silkworm with homozygous yellow silk and the silkworm with heterozygous yellow silk, and the difference in chromaticity and color fastness of yellow silk. Background technique [0002] Silkworm (Bombyx mori), also known as silkworm, is an insect that is industrially used to produce silk protein fibers in large quantities. Silk is a continuous long fiber that is solidified by secreting silk liquid when cooked silkworms make cocoons, also known as cocoon silk. The modern cocoon and silk industry mainly uses the white ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68C12N15/11
Inventor 徐世清牛艳山司马杨虎陈息林殷为民袁红霞邢瑞
Owner SUZHOU UNIV
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