Ohtsubo M, Kai R, Furuno N, Sekiguchi T, Sekiguchi M, Hayashida H, Kuma K, Miyata T, Fukushige S, Murotsu T
Laboratory of Molecular Genetics, Faculty of Science, Kyushu University, Fukuoka, Japan.
Genes Dev. 1987 Aug;1(6):585-93. doi: 10.1101/gad.1.6.585.
The human RCC1 gene was cloned after DNA-mediated gene transfer into the tsBN2 cell line, which shows premature chromosome condensation at nonpermissive temperatures (39.5-40 degrees C). This gene codes for a 2.5-kb poly(A)+ RNA that is well conserved in hamsters and humans. We isolated 15 cDNA clones from the Okayama-Berg human cDNA library, and found two that can complement the tsBN2 mutation with an efficiency comparable to that of the genomic DNA clone. The base sequences of these two active cDNA clones differ at the 5' proximal end, yet both have a common open reading frame, encoding a protein of 421 amino acids with a calculated molecular weight of 44,847 and with seven homologous repeated domains of about 60 amino acids. This human RCC1 gene was located to human chromosome 1 using sorted chromosomal fractions.
人类RCC1基因是在将DNA介导的基因转移到tsBN2细胞系后克隆得到的,该细胞系在非允许温度(39.5 - 40摄氏度)下会出现早熟染色体凝聚。该基因编码一种2.5 kb的聚腺苷酸化RNA,在仓鼠和人类中高度保守。我们从冈山县-伯格人类cDNA文库中分离出15个cDNA克隆,发现其中两个能够以与基因组DNA克隆相当的效率互补tsBN2突变。这两个活性cDNA克隆的碱基序列在5'近端有所不同,但都有一个共同的开放阅读框,编码一个421个氨基酸的蛋白质,计算分子量为44,847,具有七个约60个氨基酸的同源重复结构域。利用分选的染色体组分,将该人类RCC1基因定位到人类1号染色体上。