Uchiyama Yukinobu, Hatanaka Masami, Kimura Seisuke, Ishibashi Toyotaka, Ueda Tadamasa, Sakakibara Yoshikiyo, Matsumoto Takashi, Furukawa Tomoyuki, Hashimoto Junji, Sakaguchi Kengo
Department of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Gene. 2002 Jul 24;295(1):19-26. doi: 10.1016/s0378-1119(02)00822-3.
DNA polymerase delta (pol delta), which is comprised of at least two essential subunits, is an important enzyme involved in DNA replication and repair. We have cloned and characterized both the catalytic and small subunits of pol delta from rice (Oryza sativa L. cv. Nipponbare). The open reading frames of OsPoldelta1 and delta2 encoded a predicted product of 1105 amino acid residues with a molecular weight of 124 kDa for OsPoldelta1, and of 429 residues with a molecular weight of 48 kDa for OsPoldelta2. Northern blotting analysis indicated that OsPoldelta1 and delta2 transcripts were expressed strongly in proliferating tissues such as shoot apical meristem. The expression patterns of both subunits in the organs were slightly different. Therefore, we analyzed the spatial distribution pattern of OsPoldelta1 transcripts by in situ hybridization. In the shoot apex, OsPoldelta1 mRNA was abundant in the shoot apical meristem. In the roots, the OsPoldelta1 transcript accumulated at high levels in the root apical meristem. In mature leaves, OsPoldelta1 was induced after UV irradiation, but OsPoldelta2 was not. The amounts of the OsPoldelta1 and delta2 mRNAs in the rice cells changed rapidly during cell proliferation. These results indicated that the levels of OsPoldelta expression are markedly correlated with cell proliferation, and that some of OsPoldelta might have special roles in the leaves.
DNA聚合酶δ(pol δ)由至少两个必需亚基组成,是参与DNA复制和修复的重要酶。我们已经从水稻(日本晴)中克隆并鉴定了pol δ的催化亚基和小亚基。OsPoldelta1和delta2的开放阅读框分别编码一个预测产物,OsPoldelta1为1105个氨基酸残基,分子量为124 kDa;OsPoldelta2为429个残基,分子量为48 kDa。Northern印迹分析表明,OsPoldelta1和delta2转录本在增殖组织如茎尖分生组织中强烈表达。两个亚基在器官中的表达模式略有不同。因此,我们通过原位杂交分析了OsPoldelta1转录本的空间分布模式。在茎尖,OsPoldelta1 mRNA在茎尖分生组织中丰富。在根中,OsPoldelta1转录本在根尖分生组织中高水平积累。在成熟叶片中,紫外线照射后OsPoldelta1被诱导,但OsPoldelta2未被诱导。水稻细胞中OsPoldelta1和delta2 mRNA的量在细胞增殖过程中迅速变化。这些结果表明,OsPoldelta的表达水平与细胞增殖明显相关,并且OsPoldelta中的一些可能在叶片中具有特殊作用。