Sheng Wu Gong Cheng Xue Bao
August 2022
To study the molecular mechanism of salt stress response of peanut small GTP binding protein gene , a 1 914 bp promoter fragment upstream of the start codon of gene (-P) from peanut was cloned. Subsequently, five truncated fragments (-P1--P5) with lengths of 1 729, 1 379, 666, 510 and 179 bp were obtained through deletion at the 5' end, respectively. Plant expression vectors where these six promoter fragments were fused with the gene were constructed and transformed into tobacco by -mediated method, respectively.
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