Cloning and expression pattern of phosphate transporter 1;1 cDNA sequence from Spirodela polyrrhiza.

Zhiwei Deng; Wei Peng; Ziqing LU; Minghui FU

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Cloning and expression pattern of phosphate transporter 1;1 cDNA sequence from Spirodela polyrrhiza.

Author: Zhiwei DENG ¹ ; Wei PENG ¹ ; Ziqing LU ¹ ; Minghui FU ¹
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1. School of Biomedicine Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou 510006, Guangdong, China.
Publication Type:Journal Article
Keywords: SpPHT1; 1; Spirodela polyrrhiza; amplify; expression
MeSH: Araceae/genetics*; Biodegradation, Environmental; Cloning, Molecular; DNA, Complementary; Phosphate Transport Proteins/genetics*
From: Chinese Journal of Biotechnology 2021;37(7):2474-2482
CountryChina
Language:Chinese
Abstract: Spirodela polyrrhiza is a floating plant widely used in biomass utilization and eutrophication phytoremediation. It becomes a common aquatic plant everywhere with the increasingly serious eutrophication. It has been reported that S. polyrrhiza has a good effect on the remediation of eutrophication water. In order to study the absorption and transportation of phosphorus in S. polyrrhiza, we extracted RNA from S. polyrrhiza and then reverse transcribed it into cDNA, which was used as a template to amplify a specific fragment. The full-length sequence of the open reading frame (ORF) was 1 620 bp, encoding 539 amino acids, named SpPHT1;1, and the accession number in GenBank was MN720003. Bioinformatical analysis showed that SpPHT1;1 had no intron. The protein it encoded was a stable, hydrophobic protein with 11 transmembrane domains. SpPHT1;1 structure was similar to that of major facilitator superfamily (MFS) superfamily members. The cluster analysis showed that SpPHT1;1 was closely related to ZMPHT2 in maize and SBPHT1-8 in sorghum. So, it might belong to plant PHT1 family. The expression of SpPHT1;1 in leaf was significantly more than that of root under normal phosphorus condition. Low phosphorus condition could promote gene expression, and the relative expression level of SpPHT1;1 arrived at the peak at 48 h both in root and leaf. High phosphorus condition could inhibit gene expression. These results indicated that SpPHT1;1 expression would be affected by external phosphorus concentration. The results of this study are helpful for further research on the function of phosphate transporter. It also can provide theoretical basis for further development and utilization of S. polyrrhiza.