2009Anhui nongye kexueRequires access

Cloning of Pollen Fertility Gene MS2 and Construction of Its RNAi Expression Vector

Wenfeng Wang

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Abstract

[Objective]The aim was to study the function of MS2 gene.[Method] Cotton pollen fertility(MS2) gene cDNA fragment was cloned by RT-PCR;the senseMS2gene and antisense cDNAs of MS2 gene were ligated with the first intron of cotton chinase gene;the three fragments-fused sequence was identified and inserted into the plant expression vector of PBI121.[Result] The RNAi vector P35S12MSIn of MS2 gene was successfully constructed.[Conclusion]The vector created the conditions for genetic transformation in cotton sterile material.

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[Objective]The aim was to study the function of MS2 gene.[Method] Cotton pollen fertility(MS2) gene cDNA fragment was cloned by RT-PCR;the senseMS2gene and antisense cDNAs of MS2 gene were ligated with the first intron of cotton chinase gene;the three fragments-fused sequence was identified and inserted into the plant expression vector of PBI121.[Result] The RNAi vector P35S12MSIn of MS2 gene was successfully constructed.[Conclusion]The vector created the conditions for genetic transformation in cotton sterile material.

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Available abstract

[Objective]The aim was to study the function of MS2 gene.[Method] Cotton pollen fertility(MS2) gene cDNA fragment was cloned by RT-PCR;the senseMS2gene and antisense cDNAs of MS2 gene were ligated with the first intron of cotton chinase gene;the three fragments-fused sequence was identified and inserted into the plant expression vector of PBI121.[Result] The RNAi vector P35S12MSIn of MS2 gene was successfully constructed.[Conclusion]The vector created the conditions for genetic transformation in cotton sterile material.

Key concepts: Gene, Cloning (programming), Biology, RNA interference, Complementary DNA, Transformation (genetics), Genetics, Intron

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