Abstract

Aquaporins are water channel proteins that facilitate the passage of water through biological membranes and play a crucial role in plant growth. We showed that ethylene treatment significantly reduced petal size, inhibited expansion of petal abaxial subepidermal cells, and decreased petal water content in rose (Rosa hybrida 'Samantha'). Here, we report the isolation of a plasma membrane aquaporin (PIP) gene, Rh-PIP2;1, and characterized its potential role in ethylene-inhibited petal expansion. Rh-PIP2;1 is mainly localized on the plasma membrane and belongs to the class 2 subfamily of PIP proteins. We show that Rh-PIP2;1 is an active water channel. The transcripts of Rh-PIP2;1 are highly abundant in petal epidermal cells, especially in the abaxial subepidermal cells. The expression of Rh-PIP2;1 is highly correlated with petal expansion and tightly down-regulated by ethylene. Furthermore, we demonstrate that in Rh-PIP2;1-silenced flowers, petal expansion was greatly inhibited and anatomical features of the petals were similar to those of ethylene-treated flowers. We argue that Rh-PIP2;1 plays an important role in petal cell expansion and that ethylene inhibits petal expansion of roses at least partially by suppressing Rh-PIP2;1 expression.

Highlights

  • Aquaporins are water channel proteins that facilitate the passage of water through biological membranes and play a crucial role in plant growth

  • We found that ethylene significantly reduced petal size and water content in roses and inhibited petal expansion by inhibiting cell expansion

  • Ethylene treatment resulted in interlocking abaxial subepidermis (AbsE) cells of irregular shape, suggesting that normal cell polar expansion might be impeded by ethylene (Fig. 2B). These results indicated that ethylene inhibited petal expansion, at least partially, through the inhibition of AbsE cell expansion

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Summary

RESULTS

Effects of ethylene on petal expansion during flower opening. Our results showed that ethylene treatment resulted in vertically compressed flowers with decreased flower height-to-flower diameter ratio in rose (Rosa hybrida ‘Samantha’). Petal growth during flower opening is driven mainly by cell expansion, a process of rapid water uptake. Ethylene treatment substantially decreased the petal fresh weight, while 1-MCP significantly increased the fresh weight. BQ104371) showed approximately 20-fold increase in expression in rose petals during the early period of flower opening, according to a microarray analysis (Guterman et al, 2002) We characterized this EST for its functional role in rose petal expansion. On average, the Pf value of leaf protoplasts in transgenic plants was significantly higher than that in the wild type (14.4 and 6.6, respectively; P , 0.01) After 3 d of flower opening, when the petal expansion process was almost completed (Fig. 6B)

DISCUSSION
Findings
MATERIALS AND METHODS
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