Pfl. Chang et al., ALTERATIONS IN CELL-MEMBRANE STRUCTURE AND EXPRESSION OF A MEMBRANE-ASSOCIATED PROTEIN AFTER ADAPTATION TO OSMOTIC-STRESS, Physiologia Plantarum, 98(3), 1996, pp. 505-516
Cultured tobacco cells (Nicotiana tabacum L. cv. Wisconsin 38) adapted
to NaCl exhibited significant morphological and physiological changes
. Adapted cells remained smaller and more isodiametric at maturity tha
n unadapted cells. The vacuole increased in size relative to the cytop
lasm and an extensive network of transvacuolar membrane strands develo
ped. These changes altered the surface contact area between the cytopl
asm and the vacuole substantially. In addition, the network of Hechtia
n strands that anchor the cortical structure to the cell wall became m
ore extensively branched possibly facilitating surface contact of the
cytoplasm to the extracellular matrix. Many changes in membrane protei
ns could also be identified after NaCl adaptation. In particular, a 50
-kDa protein that is associated with the plasma membrane and tonoplast
was induced during adaptation. Immunocytochemical localization indica
ted that this 50-kDa protein is associated with Golgi vesicles. By imm
unoscreening using anti-50-kDa antibody, a 1.71-kb cDNA clone (p50C) w
as isolated from a lambda-ZAP cDNA expression library. The sequence of
p50C did not show any significant identity with other genes. Because
of the very low abundance of the p50C message, quantitative reverse tr
anscription-polymerase chain reaction (RT-PCR) was used to analyze p50
C gene expression. Immunoblot and quantitative RT-PCR analyses indicat
ed that the expression of this gene is regulated developmentally since
the mRNA and protein increased with age in salt-adapted cells but dec
reased with age in unadapted cells. Also in tobacco plants, p50C mRNA
was more abundant in younger leaves than in older leaves. The gene was
responsive to NaCl in tobacco cells and to ABA in tobacco seedlings.