Magnesium （Mg^2＋） is one of the essential cations in all cells. Although the Mg^2＋ transport mechanism has been well- documented in bacteria, less is known about Mg^2＋ transporters in eukaryotes. The AtMGT gene f...Magnesium （Mg^2＋） is one of the essential cations in all cells. Although the Mg^2＋ transport mechanism has been well- documented in bacteria, less is known about Mg^2＋ transporters in eukaryotes. The AtMGT gene family encoding putative magnesium transport proteins had been described previously. We report here that one of the Arabidopsis MGT family members, the AtMGT7 gene, encodes two mRNAs that have resulted from alternative splicing variants, designated AtMGT7a and AtMGT7b. Interestingly, the two mRNA variants were expressed with different patterns with AtMG77a expressing in all organs, but AtMGT7b appearing only in root and flowers. The AtMGT7a variant functionally complemented a bacterial mutant lacking Mg^2＋ transport capacity, whereas AtMGT7b did not. The 63Ni^2＋ tracer uptake analysis in the bacterial model showed that AtMGT7a mediated low-affinity transport of Mg^2＋. Consistent with the complementation assay result, 63Ni^2＋ tracer uptake analysis revealed that AtMGT7b did not transport Mg^2＋. This study therefore has identified from a higher plant the first low-affinity Mg^2＋ transporter encoded by a gene with alternatively spliced transcripts that produce proteins with distinct functions.展开更多
基金Supported by the National Natural Science Foundation of China (30370794)Hunan Provincial Natural Science Foundation for Excellent Youth Scholar (03JJY1003).
文摘Magnesium （Mg^2＋） is one of the essential cations in all cells. Although the Mg^2＋ transport mechanism has been well- documented in bacteria, less is known about Mg^2＋ transporters in eukaryotes. The AtMGT gene family encoding putative magnesium transport proteins had been described previously. We report here that one of the Arabidopsis MGT family members, the AtMGT7 gene, encodes two mRNAs that have resulted from alternative splicing variants, designated AtMGT7a and AtMGT7b. Interestingly, the two mRNA variants were expressed with different patterns with AtMG77a expressing in all organs, but AtMGT7b appearing only in root and flowers. The AtMGT7a variant functionally complemented a bacterial mutant lacking Mg^2＋ transport capacity, whereas AtMGT7b did not. The 63Ni^2＋ tracer uptake analysis in the bacterial model showed that AtMGT7a mediated low-affinity transport of Mg^2＋. Consistent with the complementation assay result, 63Ni^2＋ tracer uptake analysis revealed that AtMGT7b did not transport Mg^2＋. This study therefore has identified from a higher plant the first low-affinity Mg^2＋ transporter encoded by a gene with alternatively spliced transcripts that produce proteins with distinct functions.
