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Manipulating Sucrose Proton Symporters to Understand Phloem Loading

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Phloem vascular tissues transport sugars synthesized by photosynthesis in mature leaves by a process called phloem loading in source tissues and unloading in sink tissues. Phloem loading in source leaves is catalyzed by Suc/H+ symporters (SUTs) which are energized by proton motive force. In Arabidopsis the principal and perhaps exclusive SUT catalyzing phloem loading is AtSUC2. In mutant plants harboring a T-DNA insertion in each of the functional SUT-family members, only Atsuc2 mutants demonstrate overtly debilitated phloem transport. Analysis of a mutant allele (Atsuc2-4) of AtSUC2 with a T-DNA insertion in the second intron showed severely stunted phenotype similar to previously analyzed Atsuc2 null alleles. However unlike previous alleles Atsuc2-4 produced viable seeds. Analysis of phloem specific promoters showed that promoter expression was regulated by Suc concentration. Unlike AtSUC2p, heterologous promoter CoYMVp was not repressed under high Suc conc. Further analysis was conducted using CoYMVp to test the capacity of diverse clades in SUT-gene family for transferring Suc in planta in Atsuc2 - / - mutant background. AtSUC1 and ZmSUT1 from maize complemented Atsuc2 mutant plants to the highest level compared to all other transporters. Over-expression of the above SUTs in phloem showed enhanced Suc loading and transport, but against expectations, plants were stunted. The implications of SUT over-expression to enhance phloem transport and loading are discussed and how it induces a perception of phosphate imbalance is presented.
University of North Texas Libraries
Title: Manipulating Sucrose Proton Symporters to Understand Phloem Loading
Description:
Phloem vascular tissues transport sugars synthesized by photosynthesis in mature leaves by a process called phloem loading in source tissues and unloading in sink tissues.
Phloem loading in source leaves is catalyzed by Suc/H+ symporters (SUTs) which are energized by proton motive force.
In Arabidopsis the principal and perhaps exclusive SUT catalyzing phloem loading is AtSUC2.
In mutant plants harboring a T-DNA insertion in each of the functional SUT-family members, only Atsuc2 mutants demonstrate overtly debilitated phloem transport.
Analysis of a mutant allele (Atsuc2-4) of AtSUC2 with a T-DNA insertion in the second intron showed severely stunted phenotype similar to previously analyzed Atsuc2 null alleles.
However unlike previous alleles Atsuc2-4 produced viable seeds.
Analysis of phloem specific promoters showed that promoter expression was regulated by Suc concentration.
Unlike AtSUC2p, heterologous promoter CoYMVp was not repressed under high Suc conc.
Further analysis was conducted using CoYMVp to test the capacity of diverse clades in SUT-gene family for transferring Suc in planta in Atsuc2 - / - mutant background.
AtSUC1 and ZmSUT1 from maize complemented Atsuc2 mutant plants to the highest level compared to all other transporters.
Over-expression of the above SUTs in phloem showed enhanced Suc loading and transport, but against expectations, plants were stunted.
The implications of SUT over-expression to enhance phloem transport and loading are discussed and how it induces a perception of phosphate imbalance is presented.

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