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THE PLANT CELL, Vol 8, Issue 7 1181-1191, Copyright © 1996 by American Society of Plant Biologists

RESEARCH ARTICLES

The Major Integral Proteins of Spinach Leaf Plasma Membranes Are Putative Aquaporins and Are Phosphorylated in Response to Ca2+ and Apoplastic Water Potential

I. Johansson, C. Larsson, B. Ek and P. Kjellbom
Department of Plant Biochemistry, Lund University, P.O. Box 117, S-221 00 Lund, Sweden

We show that homologs of the major intrinsic protein (MIP) family are major integral proteins of the spinach leaf plasma membrane and constitute ~20% of integral plasma membrane protein. By using oligonucleotide primers based on partial amino acid sequences for polymerase chain reaction and screening of a spinach leaf cDNA library, we obtained two full-length clones of MIP homologs (pm28a and pm28b). One of these clones, pm28a, was sequenced, and it encodes a protein (PM28A) of 281 amino acids with a molecular mass of 29.9 kD. DNA gel blots indicated that PM28A is the product of a single gene, and RNA gel blots showed that pm28a is ubiquitously expressed in the plant. In vivo phosphorylation of the 28-kD polypeptide(s), corresponding to PM28A and PM28B, was dependent on apoplastic water potential, suggesting a role in regulation of cell turgor for these putative aquaporins. In vitro, only one of the homologs, PM28A, was phosphorylated. Phosphorylation of PM28A occurred on Ser-274, seven amino acids from the C terminus of the protein, within a consensus phosphorylation site (Ser-X-Arg) for vertebrate protein kinase C. In vitro phosphorylation of PM28A was due to a plasma membrane-associated protein kinase and was strictly dependent on submicromolar concentrations of Ca2+.


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