Yamaguchi Hirotaka, Nishizawa Naoko-Kishi, Nakanishi Hiromi, Mori Satoshi
Laboratory of Plant Molecular Physiology, Department of Applied Biological Chemistry, The University of Tokyo, 1-1 Yayoi, Bunkyo-ku, 113-8657 Tokyo, Japan.
J Exp Bot. 2002 Apr;53(369):727-35. doi: 10.1093/jexbot/53.369.727.
A new Fe-deficiency-induced cDNA, IDI7, was isolated from the roots of Fe-deficient barley (Hordeum vulgare L. cv. Ehimehadaka no. 1). The transcript levels of IDI7 in roots strongly correlated with iron nutritional status, and induction by Fe-deficiency was restricted to roots. Excess treatment with heavy metal ions, such as copper, manganese, and zinc, did not cause obvious IDI7 induction in either leaves or roots. IDI7 encodes a 644 amino acid protein, and has features typical of ATP-binding cassette (ABC) transporters. Phylogenetic analysis revealed that IDI7 is closely related to the half-type ABC protein subfamily, which includes mammalian transporters associated with antigen processing (TAPs). A transiently expressed fusion protein of IDI7 to green fluorescent protein (GFP) was localized to tonoplasts in suspension-cultured tobacco (Nicotiana tabacum L.) cells. IDI7 and its orthologues are thought to comprise a new class of ABC transporters, located in the tonoplasts of higher plants. A possible Fe-deficiency adaptation role for IDI7 in barley root cells, involving transport across the tonoplast, is proposed.
从缺铁大麦(Hordeum vulgare L. cv. Ehimehadaka no. 1)的根中分离出一种新的缺铁诱导cDNA,即IDI7。IDI7在根中的转录水平与铁营养状况密切相关,且缺铁诱导仅限于根。用重金属离子如铜、锰和锌过量处理,在叶和根中均未引起明显的IDI7诱导。IDI7编码一个644个氨基酸的蛋白质,具有ATP结合盒(ABC)转运蛋白的典型特征。系统发育分析表明,IDI7与半型ABC蛋白亚家族密切相关,该亚家族包括与抗原加工相关的哺乳动物转运蛋白(TAPs)。IDI7与绿色荧光蛋白(GFP)的瞬时表达融合蛋白定位于悬浮培养烟草(Nicotiana tabacum L.)细胞的液泡膜上。IDI7及其直系同源物被认为构成了一类新的ABC转运蛋白,位于高等植物的液泡膜上。提出了IDI7在大麦根细胞中可能的缺铁适应作用,涉及跨液泡膜的转运。