Nakazono M, Nishiwaki S, Tsutsumi N, Hirai A
Laboratory of Radiation Genetics, Faculty of Agriculture, University of Tokyo, Japan.
Mol Gen Genet. 1996 Sep 25;252(4):371-8. doi: 10.1007/BF02173001.
The chloroplast-derived sequence trnS-rps4/ 3'trnL-trnF-ndhJ-ndhK (4066 bases in length) is present in a region that starts 355 bases upstream of the gene for subunit 9 of NADH dehydrogenase (nad9) in the mitochondrial genome of rice. Northern blot hybridization revealed that three large transcripts of 3.05, 1.62 and 1.05 kb hybridized to strand-specific probes for both the nad9 gene and the chloroplast-derived sequence, indicating that the nad9 gene was transcribed together with the chloroplast-derived sequence. From the results of in vitro capping and ribonuclease protection experiments, as well as primer extension analysis, we identified at least seven sites for the initiation of transcription of nad9 in the chloroplast-derived sequence. All of the initiation sites for transcription of the nad9 gene were located in sequences homologous to chloroplast DNA. Two of seven initiation sites were flanked by a sequence homologous to the consensus promoter motif that includes the CRTA motif (where R is A or G) of the rice mitochondrion. However, the sequences surrounding the other five sites showed only limited similarity to the conserved sequence. It is suggested that all the promoters of the rice nad9 gene exist in a sequence that was transferred from the chloroplast during evolution. Thus, the chloroplast-derived sequence has a novel, significant function in the mitochondrial genome of this higher plant.
叶绿体衍生序列trnS-rps4/3'trnL-trnF-ndhJ-ndhK(长度为4066个碱基)存在于水稻线粒体基因组中烟酰胺腺嘌呤二核苷酸脱氢酶亚基9(nad9)基因上游355个碱基处开始的区域。Northern印迹杂交显示,3.05、1.62和1.05 kb的三个大转录本与nad9基因和叶绿体衍生序列的链特异性探针杂交,表明nad9基因与叶绿体衍生序列一起转录。通过体外加帽和核糖核酸酶保护实验以及引物延伸分析的结果,我们在叶绿体衍生序列中鉴定出至少七个nad9转录起始位点。nad9基因的所有转录起始位点都位于与叶绿体DNA同源的序列中。七个起始位点中的两个两侧是与水稻线粒体包含CRTA基序(其中R为A或G)的共有启动子基序同源的序列。然而,其他五个位点周围的序列与保守序列仅显示出有限的相似性。有人认为,水稻nad9基因的所有启动子都存在于进化过程中从叶绿体转移而来的序列中。因此,叶绿体衍生序列在这种高等植物的线粒体基因组中具有新的、重要的功能。