The neomycin phosphotransferase II (nptII) and hygromycin
phosphotransferase II (hptII) genes, originally isolated from E. coli are
widely used as selectable markers in transgenic research. The recovery of
transgenic plants in the presence of respective selection agent has been
greatly facilitated by these genes. The nptII gene confers transgenic plants
resistance to the antibiotic, kanamycin, kan, and the hptII gene provides
transgenic plants resistance to the antibiotic, hygromycin, hyg.
These
antibiotics normally inhibit protein synthesis in plants by binding to
ribosomes. However, in the transgenic plants, the encoded enzymes, NPTII and HPTII catalyze the phosphorylation of kan and hyg respectively, once they enter into plant cells. The phosphorylated kan and hyg are inactive and therefore,
unable to shut down the protein synthesis machinery in plants. This enables
transgenic plants to grow in the presence of these antibiotics. Because there
is no endogenous NPTII or HPTII activity in plants, these antibiotics can
normally inhibit the growth of non-transgenic plants.
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