棉 花 学 报 Cotton Science 2007，19(3):163-167
Expression of GUS Gene and NPTII Gene and Their Application in the Detecting of Transgenic Cotton Abstract：By Agrobacterium-mediated method，the plant expression vector contained the target gene FB driven by a cotton fiber specific expression promoter E6 was transferred into cotton cultivar R15. The vector also contains a GUS gene，and a NPTII gene driven by 35S promoter，respectively. The expression of GUS gene and NPTII gene was analyzed in the stage of resistant calli selected，T0 and T1 generation transgenic plants. These two genes are in the same T-DNA in the vector，their expression has high relativity. Because the phenomena of transgenic silencing and the effect of insert sites，the expression of GUS gene and NPTII gene has some differences. We obtained the resistant calli through detecting the expression of GUS gene and NPTII gene together. Kanamycin resistance，GUS staining，and PCR detection were conducted on the 15 putative T0 generation transgenic plants. Among them，11 plants were positive for the transgene according T0 PCR detection，the positive ratio reached 73.3%. 12 plants showed kanamycin resistance，10 plants were GUS-staining positive，the expression of NPTII gene and GUS gene showed high relativity.10 positive plants were obtained through the three detected methods among the 15 T0 generation transgenic plants. The breeding of transgenic progeny also relied on both kanamycin examination and GUS staining. Of T1 transgenic progeny，the expression of GUS gene and NPTII gene has significant difference，so there has some limitation for T0 as a certain extent for screening the transgenic progeny only by kanamycin examination. Kanamycin assay was performed in the field， climate and other circumstance -factors may influence the result. However，being simple and fast，this assay can employed as a preliminary screen，three times of kanamycin assay were performed during the period of cotton vegetable development，and then GUS staining were acted based on the result of kanamycin resistant test. Proceeded the two methods together，the limitation of each measure can be compensated ， accordingly the efficiency of homozygous breeding of transgenic progeny could be increase obviously. Seven T1 generation transgenic lines were all in accordance with Mendelian patterns of inheritance in the ratio of resistant plants T0 non-resistant plants through kanamycin assay and GUS staining.
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