Abstract

Because the photosynthetic apparatus contains a massive amount of nitrogen in plants, the regulation of its development by sugar signals is important to the maintenance of the carbon-nitrogen balance. In this study we isolated an Arabidopsis mutant (sicy-192) whose cotyledon greening was inhibited by treatments with sugars such as sucrose, glucose, and fructose. In the mutant, the gene encoding plastidic alkaline/neutral invertase (INV-E) was point-mutated at codon 294, with Tyr substituted for Cys (C294Y). Interestingly, the greening of cotyledons in the knock-out INV-E lines was not inhibited by treatment with the sugars. In addition, the knock-out INV-E lines expressing an INV-E:C294Y or INV-E:C294A gene had the same phenotype as sicy-192 mutants, whereas the lines expressing a wild-type INV-E gene had the same phenotype as wild-type plants. A recombinant INV-E:C294Y protein had the same enzymatic activity as a recombinant INV-E protein, suggesting that the Cys-294 residue of INV-E is important for its functions in the chloroplasts. On treatment with sucrose, the expression of photosynthesis-related genes was weaker in seedlings of mutant plants than wild-type seedlings, whereas the activity of nitrate reductase was stronger in the mutant plants than wild-type plants. These findings suggest that Cys-294 of INV-E is associated with the development of the photosynthetic apparatus and the assimilation of nitrogen in Arabidopsis seedlings to control the ratio of sucrose content to hexose content.

Highlights

  • Technology Project of the Japan Science and Technology Agency

  • The greening of cotyledons of sicy-192 mutant plants was inhibited by treatment with sucrose and with glucose or fructose (Fig. 1B)

  • The photosynthetic apparatus contains a massive amount of nitrogen, and its development closely depends on the distribution of nitrogen in plants (1–4)

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Summary

Introduction

Technology Project of the Japan Science and Technology Agency The transcript level of INV-E in sicy-192 mutants was almost the same as that in wild-type plants (Fig. 3A). The protein levels of INV-E in the mutants were higher than those in the wild-type plants (Fig. 3C).

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