Abstract:
Based on the expression vector pBI121, we successfully constructed a plant overexpression vector of Hspa4 gene
fusing with selective maker gene (hygromycin-resistance gene) driven by the Ubi-1 promoter (pBI121-Ubi-Hpt-Hspa4,
p121UHH). The plant expression vectors p121UHH and pCAMBIA1301-Ubi-Hspa4 (p1301UH) were transformed into the
rice callus, mediated by Agrobacterium tumefaciens. We screened 17 p121UHH-positive transgenic plants and 15
p1301UH-positive transgenic plants by the hygromycin-resistance gene. The pick-up rate of the resistance callus was 51.7%
and 42.5%, respectively, and the rate of regeneration for the resistance callus was 51.2% and 49.1%, respectively. The result
of polymerase chain reaction (PCR) identification indicated that the pick-up rate of positive transgenic plants was 51.7% and
42.5% and the total transformation efficiency was 16.5% and 6.2%, and the former was 2.66 times of the later. The results
of the experiment indicate that the possibility of the appearance of false positive results in the fusing of a plant overexpression vector with a selective maker gene is much less
