Two Members of the Aluminum-Activated Malate Transporter Family,SlALMT4andSlALMT5, are Expressed during Fruit Development, and the Overexpression ofSlALMT5Alters Organic Acid Contents in Seeds in Tomato (Solanum lycopersicum)
Author(s) -
Takayuki Sasaki,
Yoshiyuki Tsuchiya,
Michiyo Ariyoshi,
Ryohei Nakano,
Koichiro Ushijima,
Yasutaka Kubo,
Izumi C. Mori,
Emi Higashiizumi,
Ivan Gális,
Yoko Yamamoto
Publication year - 2016
Publication title -
plant and cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.975
H-Index - 152
eISSN - 1471-9053
pISSN - 0032-0781
DOI - 10.1093/pcp/pcw157
Subject(s) - subcellular localization , gene , biology , gene family , endoplasmic reticulum , biochemistry , microbiology and biotechnology , promoter , xenopus , gene expression , transporter
The aluminum-activated malate transporter (ALMT) family of proteins transports malate and/or inorganic anions across plant membranes. To demonstrate the possible role of ALMT genes in tomato fruit development, we focused on SlALMT4 and SlALMT5, the two major genes expressed during fruit development. Predicted proteins were classified into clade 2 of the family, many members of which localize to endomembranes. Tissue-specific gene expression was determined using transgenic tomato expressing the β-glucuronidase reporter gene controlled by their own promoters. Both the genes were expressed in vascular bundles connecting to developing seeds in fruit and in the embryo of mature seeds. Further, SlALMT5 was expressed in embryo in developing seeds in fruit. Subcellular localization of both proteins to the endoplasmic reticulum (ER) was established by transiently expressing the green fluorescent protein fusions in plant protoplasts. SlALMT5 probably localized to other endomembranes as well. Localization of SlALMT5 to the ER was also confirmed by immunoblot analysis. The transport function of both SlALMT proteins was investigated electrophysiologically in Xenopus oocytes. SlALMT5 transported malate and inorganic anions such as nitrate and chloride, but not citrate. SlALMT4 also transported malate, but the results were less consistent perhaps because it did not localize strongly to the plasma membrane. To elucidate the physiological role of SlALMT5 further, we overexpressed SlALMT5 in tomato. Compared with the wild type, overexpressors exhibited higher malate and citrate contents in mature seeds, but not in fruit. We conclude that the malate transport function of SlALMT5 expressed in developing fruit influences the organic acid contents in mature seeds.
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