Selection of Arabidopsis transformants containing AtZAT12

C. T. T. Le, N. T. Pham
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Abstract

This study aimed to select Arabidopsis seeds after transformation with the AtZAT12 gene via Agrobacterium tumerfaciens. ZAT12 is a transcription factor that inhibits other transcription factors FIT through the EAR motif. FIT itself is a central transcription factor that controls Fe uptake under Fe-deficient conditions. However, if Fe is absorbed excessively, it will produce reactive oxygen species that could damage cells. That is the reason why AtZAT12 transcription is elevated and FIT transcription is inhibited under Fe deficiency for 10 days. To investigate the function, the AtZAT12 gene was inserted into the pMDC107 vector for transformation into Arabidopsis. The T0 Arabidopsis seeds obtained after floral dip transformation were placed on 1% MS agar supplemented with 15 μg/mL Hygromycin B. Beforehand, the T0 seeds were sterilized and kept in the dark for stratification. Subsequently, the seed plates were subjected to a regime of 6 h of light, 48 h of dark and 24 h of light (3.25 d). The hygromycin B-resistant seedlings had long hypocotyls (~ 1.0 cm), while the non-resistant seedlings had short (~ 0.3 cm) hypocotyls. This method took only 3.25 days to identify transgenic Arabidopsis seedlings. After that, positive transgene lines were examined by PCR method for AtZAT12, and the expression of AtZAT12 was observed under microscope.
含AtZAT12的拟南芥转化子的筛选
本研究旨在筛选经农杆菌转化AtZAT12基因的拟南芥种子。ZAT12是一种通过EAR基序抑制其他转录因子FIT的转录因子。FIT本身是在缺铁条件下控制铁摄取的中心转录因子。然而,如果铁被过度吸收,它会产生活性氧,可能会损害细胞。这就是缺铁10天AtZAT12转录升高,FIT转录抑制的原因。为了研究AtZAT12基因的功能,我们将AtZAT12基因插入到pMDC107载体中,并将其转化为拟南芥。将花浸转化后的T0粒拟南芥种子置于添加15 μg/mL潮霉素b的1% MS琼脂上,灭菌后置于暗处分层。随后,将种子板置于光照6 h、黑暗48 h和光照24 h (3.25 d)的环境中。耐潮霉素b的幼苗下胚轴长(~ 1.0 cm),而不耐潮霉素b的幼苗下胚轴短(~ 0.3 cm)。该方法鉴定转基因拟南芥幼苗仅需3.25天。用PCR法检测AtZAT12转基因阳性系,并在显微镜下观察AtZAT12的表达情况。
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