Noda A
Research Division for Cellular Regulation, Meiji Cell Technology Center, Odawara, Japan.
Somat Cell Mol Genet. 1992 Mar;18(2):113-22. doi: 10.1007/BF01233158.
The autosomal recessive genetic disorder ataxia telangiectasia (AT) has been characterized in the RNA transcripts of cultured cells. Molecular species of poly (A)+ RNA that are present in AT fibroblasts (ATFs) at levels different from those in normal human fibroblasts (NHFs) were cloned in the form of cDNAs. Treatment with bleomycin, which transiently inhibits DNA synthesis in NHFs but not in ATFs, differentiated ATFs and NHFs in the above cloning. Two cDNA clones with an identical DNA sequence were isolated, the corresponding RNA transcript of which was induced approximately twofold after bleomycin treatment in NHFs, but not in ATFs. The DNA sequence of these two cDNA clones, except for its polyadenylation part, was identical to the heavy-strand replication origin sequence of human mitochondrial DNA. The results indicate the possibility that the induction of this RNA transcript is involved in bleomycin-induced inhibition of DNA synthesis in normal human cells, while it is defective in AT cells. In addition, the previous observation that much fibronectin is produced in AT cells was confirmed in this study in terms of RNA transcription.
常染色体隐性遗传病共济失调毛细血管扩张症(AT)已在培养细胞的RNA转录物中得到表征。以cDNA的形式克隆了AT成纤维细胞(ATF)中存在的、与正常人成纤维细胞(NHF)水平不同的聚腺苷酸加尾RNA(poly (A)+ RNA)分子种类。博来霉素处理可短暂抑制NHF中的DNA合成,但不抑制ATF中的DNA合成,在上述克隆过程中区分了ATF和NHF。分离出两个具有相同DNA序列的cDNA克隆,其相应的RNA转录物在NHF中经博来霉素处理后诱导增加约两倍,但在ATF中未增加。这两个cDNA克隆的DNA序列,除其聚腺苷酸化部分外,与人类线粒体DNA的重链复制起始序列相同。结果表明,这种RNA转录物的诱导可能参与博来霉素诱导的正常人细胞DNA合成抑制,而在AT细胞中存在缺陷。此外,本研究在RNA转录方面证实了先前观察到的AT细胞中产生大量纤连蛋白的现象。