Each cotton fiber is a single cell that elongates to 2.5 to 3.0 cm from the seed coat epidermis within ف 16 days after anthesis (DAA). To elucidate the mechanisms controlling this rapid elongation, we studied the gating of fiber plasmodesmata and the expression of the cell wall-loosening gene expansin and plasma membrane transporters for sucrose and K ؉ , the major osmotic solutes imported into fibers. Confocal imaging of the membrane-impermeant fluorescent solute carboxyfluorescein (CF) revealed that the fiber plasmodesmata were initially permeable to CF (0 to 9 DAA), but closed at ف 10 DAA and re-opened at 16 DAA. A developmental switch from simple to branched plasmodesmata was also observed in fibers at 10 DAA. Coincident with the transient closure of the plasmodesmata, the sucrose and K ϩ transporter genes were expressed maximally in fibers at 10 DAA with sucrose transporter proteins predominately localized at the fiber base. Consequently, fiber osmotic and turgor potentials were elevated, driving the rapid phase of elongation. The level of expansin mRNA, however, was high at the early phase of elongation (6 to 8 DAA) and decreased rapidly afterwards. The fiber turgor was similar to the underlying seed coat cells at 6 to 10 DAA and after 16 DAA. These results suggest that fiber elongation is initially achieved largely by cell wall loosening and finally terminated by increased wall rigidity and loss of higher turgor. To our knowledge, this study provides an unprecedented demonstration that the gating of plasmodesmata in a given cell is developmentally reversible and is coordinated with the expression of solute transporters and the cell wall-loosening gene. This integration of plasmodesmatal gating and gene expression appears to control fiber cell elongation.
INTRODUCTIONA unique feature of cotton seed development is that ف 30% of the ovule epidermal cells initiate into fibers from the outermost layer of integument at anthesis (See Figure 1A). Each cotton fiber is a single cell and elongates from 10 to 15 m up to 2.5 to 3.0 cm by ف 16 days after anthesis (DAA) before it switches to secondary cell wall cellulose synthesis (Basra and Malik, 1984;Tiwari and Wilkins, 1995). The rate of fiber elongation and the final length attained are well above that commonly seen for plant cells (Cosgrove, 1997) and render it perhaps the longest single cell in higher plants. Thus, the cotton fiber represents a unique system in which to study not only carbon partitioning to cellulose synthesis (Delmer and Amor, 1995;Ruan et al., 1997) but also the control of cell elongation without the complication of cell division and multicellular development. Apart from its significance in understanding basic cell biology, elucidating the cellular and molecular basis of fiber elongation could also identify potential targets for genetic manipulation of fiber length, a key determinant of fiber yield and quality.The rapid fiber elongation is believed to be driven by high turgor (Dhindsa et al., 1975;Ruan and Chourey, 1998;Smart et al., 19...