Group of bemisia tabaci prevention and control target genes and combined application thereof
A technology of bemisia tabaci and target genes, applied in application, genetic engineering, plant genetic improvement, etc., can solve the problem of unsatisfactory control effect of bemisia tabaci, endangering ecological environment food safety, and insecticide resistance level of bemisia tabaci Increase and other issues
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Embodiment 1
[0019] Example 1: Effects of Feeding dsRNAs on the Survival Rate of Bemisia tabaci Adults
[0020] 1. Design specific primers for BtGlu gene, BtArgH gene and BtTK gene (see SEQ ID NO.4~SEQ ID NO.9 respectively for its sequence information), and use cDNA as template amplification to obtain double-stranded DNA (abbreviated as BtGlu, BtArgH and BtTK), its sequence information is shown in SEQ ID NO.1 (5'→3'), SEQ ID NO.2 (5'→3'), SEQ ID NO.3 (5'→3');
[0021] 2. Using the double-stranded DNA obtained by the in vitro reverse transcription method as a template, the double-stranded RNA (dsBtGlu, dsBtArgH and dsBtTK for short) was synthesized and purified by in vitro transcription method;
[0022] 3. Mix dsBtGlu, dsBtArgH and dsBtTK in equal amounts (the resulting solution is built into dsRNAs);
[0023] 4. Take a cylindrical double-pass glass tube with an inner diameter of 2 cm and a height of 5 cm, pull the Parafilm membrane to the end of the double-pass glass tube, drop 200 μl of ...
Embodiment 2
[0026] Example 2: Effect of feeding dsRNAs on egg laying rate of Bemisia tabaci females
[0027] 1. Design specific primers for BtGlu gene, BtArgH gene and BtTK gene (see SEQ ID NO.4~SEQ ID NO.9 respectively for its sequence information), and use cDNA as template amplification to obtain double-stranded DNA (abbreviated as BtGlu, BtEAAs and BtPYs), the sequence information of which is shown in SEQ ID NO.1 (5'→3'), SEQ ID NO.2 (5'→3'), SEQ ID NO.3 (5'→3');
[0028] 2. Using the double-stranded DNA obtained by the in vitro reverse transcription method as a template, double-stranded RNAs (dsBtGlu, dsBtEAAs and dsBtPYs for short) were synthesized and purified by in vitro transcription method;
[0029] 3. Mix dsBtGlu, dsBtEAAs and dsBtPYs in equal amounts (the resulting solution is built into dsRNAs);
[0030]4. Take a cylindrical double-pass glass tube with an inner diameter of 2 cm and a height of 5 cm, pull the Parafilm membrane to the end of the double-pass glass tube, drop 200...
Embodiment 3
[0035] Example 3: Effect of Feeding dsRNAs on Symbiotic Bacteria of Bemisia tabaci Females
[0036] 1. Design specific primers for BtGlu gene, BtArgH gene and BtTK gene (see SEQ ID NO.4~SEQ ID NO.9 respectively for its sequence information), and use cDNA as template amplification to obtain double-stranded DNA (abbreviated as BtGlu, BtArgH and BtTK), its sequence information is shown in SEQ ID NO.1 (5'→3'), SEQ ID NO.2(5'→3'), SEQ ID NO.3(5'→3');
[0037] 2. Using the double-stranded DNA obtained by the in vitro reverse transcription method as a template, the double-stranded RNA (dsBtGlu, dsBtArgH and dsBtTK for short) was synthesized and purified by in vitro transcription method;
[0038] 3. Mix dsBtGlu, dsBtArgH and dsBtTK in equal amounts (the resulting solution is built into dsRNAs);
[0039] 4. Take a cylindrical double-pass glass tube with an inner diameter of 2 cm and a height of 5 cm, pull the Parafilm membrane to the end of the double-pass glass tube, drop 200 μl of s...
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