Obara Keisuke, Sumi Kazuyoshi, Fukuda Hiroo
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan.
Plant Cell Physiol. 2002 Jul;43(7):697-705. doi: 10.1093/pcp/pcf103.
Monodehydroascorbate reductase (MDAR) isoforms exist in mitochondria, chloroplasts, cytosol and microbodies. Two putative MDAR sequences with an extended N-terminal region are found in Arabidopsis. They differ in the length of the extension by 21 bp. We have shown that these two isoforms arise from a single gene by the use of multiple transcription starts. Green fluorescent protein was fused to each extension, revealing that the longer and shorter fusion proteins were imported into mitochondria and chloroplasts, respectively. These results demonstrate that putative MDAR is a dual-targeting protein transported into both mitochondria and chloroplasts. Although there have been several reports of dual targeting of proteins to mitochondria and chloroplasts, this is the first example in which the dual targeting of the protein to mitochondria and chloroplasts is achieved by the use of multiple transcription initiation sites.
单脱氢抗坏血酸还原酶(MDAR)亚型存在于线粒体、叶绿体、细胞质和微体中。在拟南芥中发现了两个具有延长N端区域的假定MDAR序列。它们在延长部分的长度上相差21个碱基对。我们已经表明,这两种亚型是通过使用多个转录起始位点从单个基因产生的。绿色荧光蛋白与每个延长部分融合,结果表明较长和较短的融合蛋白分别被导入线粒体和叶绿体。这些结果证明,假定的MDAR是一种双靶向蛋白,可被转运到线粒体和叶绿体中。虽然已经有几篇关于蛋白质双靶向线粒体和叶绿体的报道,但这是第一个通过使用多个转录起始位点实现蛋白质双靶向线粒体和叶绿体的例子。