Plant Physiology Preview
Published on February 24, 2002; 10.1104/pp.010624
Received July 16, 2001
Returned for revision September 23, 2001
Accepted December 18, 2001
The Rice Mutant esp2 Greatly Accumulates the Glutelin
Precursor and Deletes the Protein Disulfide Isomerase
Yoko Takemoto , Sean J. Coughlan , Thomas W. Okita , Hikaru Satoh , Masahiro Ogawa , and Toshihiro Kumamaru *
Institute of Genetic Resources, Faculty of Agriculture, Kyushu University, Hakozaki, Fukuoka 812--8581, Japan (Y.T., H.S., T.K.); DuPont Agricultural Experimental Station, 402/4251, Wilmington, Delaware 19880--0402 (S.J.C.); Institute of Biological Chemistry, Washington State University, Pullman, Washington 99164--6340 (T.W.O.); Department of Life Science, Yamaguchi Prefectural University, Sakurabatake, Yamaguchi 753--8502, Japan (M.O.)
* Corresponding author; email: kumamaru{at}agr.kyushu-u.ac.jp.
Rice (Oryza sativa) accumulates prolamins and glutelins as storage proteins. The latter storage protein is synthesized on the endoplasmic reticulum (ER) as a 57-kD proglutelin precursor, which is then processed into acidic and basic subunits in the protein storage vacuole. Three esp2 mutants, CM1787, EM44, and EM747, contain larger amounts of the 57-kD polypeptide and corresponding lower levels of acidic and basic glutelin subunits than normal. Electron microscopic observation revealed that esp2 contained normal-appearing glutelin-containing protein bodies (PB-II), but lacked the normal prolamin-containing PB (PB-I). Instead, numerous small ER-derived PBs of uniform size (0.5 µm in diameter) and low electron density were readily observed. Immunoblot analysis of purified subcellular fractions and immunocytochemistry at the electron microscopy level showed that these new PBs contained the 57-kD proglutelin precursor and prolamin polypeptides. The 57-kD proglutelin was extracted with 1% (v/v) lactic acid solution only after removal of cysteine-rich prolamin polypeptides, suggesting that these proteins form glutelin-prolamin aggregates via interchain disulfide bonds within the ER lumen. The endosperm of esp2 mutants contains the lumenal chaperones, binding protein and calnexin, but lacks protein disulfide isomerase (PDI) at the protein and RNA levels. The transcript of PDI was expressed in the seed only during the early stage of seed development in the wild type. These results suggest that PDI plays an essential role in the segregation of proglutelin and prolamin polypeptides within the ER lumen.
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