Ittmann M, Greco A, Basilico C
Department of Pathology, New York University School of Medicine, New York 10016.
Mol Cell Biol. 1987 Oct;7(10):3386-93. doi: 10.1128/mcb.7.10.3386-3393.1987.
We have cloned the human genomic DNA and the corresponding cDNA for the gene which complements the mutation of tsBN51, a temperature-sensitive (Ts) cell cycle mutant of BHK cells which is blocked in G1 at the nonpermissive temperature. After transfecting human DNA into TsBN51 cells and selecting for growth at 39.5 degrees C, Ts+ transformants were identified by their content of human AluI repetitive DNA sequences. Following two additional rounds of transfection, a genomic library was constructed from a tertiary Ts+ transformant and a recombinant phage containing the complementing gene isolated by screening for human AluI sequences. A genomic probe from this clone recognized a 2-kilobase mRNA in human and tertiary transformant cell lines, and this probe was used to isolate a biologically active cDNA from the Okayama-Berg cDNA expression library. Sequencing of this cDNA revealed a single open reading frame encoding a polypeptide of 395 amino acids. The deduced BN51 gene product has a high proportion of acidic and basic amino acids which are clustered in four hydrophilic domains spaced at 60- to 80-amino-acid intervals. These domains have strong sequence homology to each other. Thus, the tsBN51 protein consists of periodic repetitive clusters of acidic and basic amino acids.
我们已经克隆了与tsBN51突变互补的基因的人类基因组DNA和相应的cDNA。tsBN51是BHK细胞的一种温度敏感(Ts)细胞周期突变体,在非允许温度下被阻断在G1期。将人类DNA转染到TsBN51细胞中,并选择在39.5摄氏度下生长,通过其人类AluI重复DNA序列的含量鉴定出Ts +转化体。经过另外两轮转染后,从三级Ts +转化体构建了一个基因组文库,并通过筛选人类AluI序列分离出一个含有互补基因的重组噬菌体。来自该克隆的基因组探针在人类和三级转化体细胞系中识别出一个2千碱基的mRNA,并且该探针用于从冈山县-伯格cDNA表达文库中分离出具有生物活性的cDNA。该cDNA的测序揭示了一个单一的开放阅读框,编码一个395个氨基酸的多肽。推导的BN51基因产物具有高比例的酸性和碱性氨基酸,它们聚集在四个亲水结构域中,间隔为60至80个氨基酸。这些结构域彼此具有很强的序列同源性。因此,tsBN51蛋白由酸性和碱性氨基酸的周期性重复簇组成。