Kimura S, Ueda T, Hatanaka M, Takenouchi M, Hashimoto J, Sakaguchi K
Department of Applied Biological Science, Faculty of Science and Technology, Science University of Tokyo, Chiba-ken, Japan.
Plant Mol Biol. 2000 Feb;42(3):415-27. doi: 10.1023/a:1006349511964.
Flap endonuclease-1 (FEN-1) is an important enzyme involved in DNA replication and repair. We isolated a 1.4 kb cDNA from rice (Oryza sativa), termed OsFEN-1, encoding a protein which shows homology with the eukaryotic FEN-1 proteins. OsFEN-1 protein was overexpressed in Escherichia coli and purified to near homogeneity. DNA cleavage analysis using different branched DNA structures indicated that OsFEN-1 protein possesses both 5'-flap endonuclease and 5' to 3' double-stranded DNA exonuclease activities. OsFEN-1 protein incises a 5'-flap and 5'-pseudo Y structure one base 3' of the branched point in the duplex region. The enzymatic properties indicated that we succeeded in obtaining the gene and the protein of a plant counterpart of FEN-1. OsFEN-1 transcripts were expressed strongly in proliferating tissues such as root tips and young leaves that contain root apical meristem and marginal meristem, respectively. No expression was detected in mature leaves although the leaves were exposed to UV. We analyzed the spatial distribution pattern of OsFEN-1 transcripts by in situ hybridization. In the shoot apex, OsFEN-1 mRNA was abundant in the shoot apical meristem, tiller bud, leaf primordia, ligule primordia and marginal meristem of young leaves. In the roots, the transcript accumulated to high levels in the root apical meristem. Our results indicate that OsFEN-1 is expressed in tissues rich in proliferating cells, and its expression may be required for cell growth and organ formation.
瓣内切核酸酶-1(FEN-1)是一种参与DNA复制和修复的重要酶。我们从水稻(Oryza sativa)中分离出一个1.4 kb的cDNA,命名为OsFEN-1,它编码一种与真核生物FEN-1蛋白具有同源性的蛋白质。OsFEN-1蛋白在大肠杆菌中过表达并纯化至接近均一性。使用不同分支DNA结构的DNA切割分析表明,OsFEN-1蛋白同时具有5'-瓣内切核酸酶和5'至3'双链DNA外切核酸酶活性。OsFEN-1蛋白在双链区域分支点的3'端一个碱基处切割5'-瓣和5'-假Y结构。酶学性质表明我们成功获得了FEN-1植物对应物的基因和蛋白。OsFEN-1转录本在增殖组织如根尖和幼叶中强烈表达,根尖分别含有根尖分生组织和边缘分生组织。尽管叶片暴露于紫外线,但在成熟叶片中未检测到表达。我们通过原位杂交分析了OsFEN-1转录本的空间分布模式。在茎尖,OsFEN-1 mRNA在茎尖分生组织、分蘖芽、叶原基、叶舌原基和幼叶的边缘分生组织中丰富。在根中,转录本在根尖分生组织中积累到高水平。我们的结果表明,OsFEN-1在富含增殖细胞的组织中表达,其表达可能是细胞生长和器官形成所必需的。