蔗糖转运蛋白基因VvSUC12和VvSUC27在葡萄胚性和非胚性愈伤组织中的差异表达

Differentiated expression of VvSUC12 and VvSUC27 in embryogenic and non-embryogenic calli of Vitis vinifera L.

本研究通过对霞多丽葡萄花前约10d的花丝进行组培诱导,获得胚性和非胚性两种愈伤组织,分别进行继代、组织结构观察和体细胞胚的诱导验证。为研究两种愈伤组织对培养基中主要碳源蔗糖的利用特点,根据GenBank中的定位于细胞质膜的葡萄蔗糖转运蛋白基因VvSUC12和VvSUC27的序列,设计了这两种蔗糖转运蛋白的PCR引物。以RNAplant试剂法,提取胚性愈伤组织和非胚性愈伤组织的RNA,进行半定量RT-PCR。研究表明,31个循环半定量RT-PCR结果中VvSUC12在胚性愈伤和非胚性愈伤中均有表达,且在非胚性愈伤组织中的表达水平稍高于胚性愈伤组织,表达差异未达到显著水平,VvSUC27的表达水平明显低于VvSUC12,且只在胚性愈伤组织中表达。提高至35个循环的半定量RT-PCR结果显示VvSUC27基因在非胚性愈伤组织中微弱表达,而在胚性愈伤组织中的表达强度较31个循环有所增加,且高于非胚性愈伤。

We induced embryogenic calli （EC） and non-embryogenic calli （NEC） from flower filaments of Vitis vinifera L. cv. Chardonnay about 10 days before full bloom. The callus were sub-cultured, observed and verified by somatic embryo induction. PCR primers for VvSUC12 and VvSCU27 were designed according to the corresponding sequences in GenBank. After RNA extraction with RNAplant for EC and NEC cell lines, we synthesized the 1st strand DNA for semi quantitative RT-PCR, and normalized the density of the bands against house-keeping gene Actin. The results of 31 cycles semi-quantitative RT-PCR showed that VvSUC12 was highly expressed in both EC and NEC, with higher expression intensity in NEC than in EC, but not reached the significantlevel; while the expression of VvSUC27 was only detected in EC, and the expression level was significantly lower than that of VvSUC12. We increased the semi-quantitative RT-PCR cycle number to 35 and found that VvSUC27 gene was weakly expressed in NEC, in EC the intensity of the band was increased comparing with 31 cycles, and the expression level was higher than that of NEC. The paper discussed the differential expression of the two sucrose transporters and their relationship with the sucrose in the tissue culture medium.