Expression of Multiple Exogenous Insect Resistance and Salt Tolerance Genes inPopulus nigraL.

Four exogenous genes,Cry3A,Cry1Ac, mtlD,andBADH, were inserted into the p1870 vector to obtain multigenic transgenicPopulus nigraL. with improved insect resistance and salt tolerance. During vector construction, different promoters were used for each gene, the AtADH 5 '-UTR enhancer was added between theCry1Acpromoter and the target gene, and the matrix attachment region (MAR, GenBank: U67919.1) structure was added at both ends of the vector. It was then successfully transferred into the genome of European black poplar by Agrobacterium-mediated leaf disk transformation, and a total of 28 transgenic lines were obtained by kanamycin screening. Five events with the highest insect resistance were selected based on preliminary tests: nos. 1, 7, 9, 12, and 17. PCR, real-time PCR, and enzyme-linked immunosorbent assays (ELISA) were used to detect the expression of exogenous genes and to analyze the Bt protein toxin levels in transgenic lines from June to October. PCR results showed that all four genes were successfully introduced into the five selected lines. Fluorescence quantitative PCR showed no significant differences in the transcript abundance of the four exogenous genes between different lines. A Bt protein toxin assay showed that the Cry3A protein toxin content was significantly higher than the Cry1Ac protein toxin content by approximately three orders of magnitude. Levels of the two toxins were negatively correlated. Over the course of the growing season, Cry1Ac content raised and varied between 0.46 and 18.41 ng center dot g(-1). Cry3A content decreased over the same time period and varied between 2642.75 and 15775.22 ng center dot g(-1). Indoor insect feeding assay showed that the transgenic lines had high insect resistance, with mortality rates of 1-2-year-oldHyphantria cunealarvae reaching more than 80%, and those ofPlagiodera versicoloralarvae and nymphs reaching 100%. No. 17 and no. 12 lines had better insect resistance toLepidopteraandColeopterapests. There was no clear improvement in salt tolerance of the transgenic lines, but comprehensive evaluation of 11 salt tolerance indicators showed that lines no. 17 and no. 7 had certain degrees of salt tolerance.