Philipps G, Clément B, Gigot C
Institut de Biologie Moléculaire des Plantes du CNRS, Université Louis Pasteur, Strasbourg, France.
FEBS Lett. 1995 Jan 16;358(1):67-70. doi: 10.1016/0014-5793(94)01397-j.
A cDNA clone isolated from an Arabidopsis thaliana cell suspension library showed highly significant homology to the small subunit of ribonucleotide reductase (R2) from different species. The 340 amino acid-long deduced putative protein contains all the residues that are important for the enzyme activity and structure. In A. thaliana this enzyme is encoded by a single-copy gene. In synchronized tobacco BY2 cells the corresponding mRNAs specifically accumulate during the S phase of the cell cycle.
从拟南芥细胞悬浮文库中分离出的一个cDNA克隆与来自不同物种的核糖核苷酸还原酶小亚基(R2)具有高度显著的同源性。推导的假定蛋白质长340个氨基酸,包含对酶活性和结构重要的所有残基。在拟南芥中,这种酶由单拷贝基因编码。在同步化的烟草BY2细胞中,相应的mRNA在细胞周期的S期特异性积累。