The
Arabidopsis thaliana (L.)
Heynh. SUC2 gene encodes a plasma-membrane sucrose-H
+ symporter. The DNA sequence of the
SUC2 promoter has been determined. Using a translational fusion of this promoter to the N-terminus of

-glucuronidase (GUS) and the GUS histochemical assay, the tissue specificity of the
SUC2 promoter was studied in
Arabidopsis plants transformed with this fusion construct. The
SUC2 promoter directed expression of GUS activity with high specificity to the phloem of all green tissues of
Arabidopsis such as rosette leaves, stems, and sepals. During leaf development the expression of SUC2-GUS activity was first seen in the tips of young rosette leaves. In older leaves and during their concomitant sink/source transition, expression proceeded from the tips to the bases of the leaves, indicating that expression of the SUC2 sucrose-H
+ symporter is tightly coupled to the source-strength of
Arabidopsis leaves. Expression of SUC2-GUS activity was also seen, however, in sink tissues such as roots and developing
Arabidopsis pods, suggesting that the product of the
SUC2 gene might not only be important for phloem loading, but also for phloem unloading. A possible regulatory effect of carbohydrates (glucose and sucrose) on the activity of the
SUC2 promoter was studied and excluded, both in excised leaves and young seedlings of transgenic
Arabidopsis plants. The overall pattern of SUC2-GUS expression correlated well with that of the
Arabidopsis thaliana AHA3 plasma-membrane H
+ -ATPase which is also expressed in the phloem and most likely represents the primary pump generating the energy for secondary active transporters such as SUC2.
Key words Arabidopsis - Phloem loading/unloading - Plasma membrane - Source/sink - Sucrose - H+ symport
Accession number for SUC2-promoter sequences: The DNA sequence data reported in this paper will appear in the EMBL, GenBank, and DDBJ nucleotide sequence databases under the accession number X79702 (AtSUC2 promoter sequence)
We want to thank Günther Peissig for growing the Arabidopsis thaliana plants. This work was supported by the Deutsche Forschungsgemeinschaft (SFB 43/C5) and a grant to N.S. from the Bundesministerium für Forschung und Technologie.