Fujii T, Yamaoka H, Gomi K, Kitamoto K, Kumagai C
National Research Institute of Brewing, Tokyo, Japan.
Biosci Biotechnol Biochem. 1995 Oct;59(10):1869-74. doi: 10.1271/bbb.59.1869.
A genomic DNA encoding ribonuclease (RNase) T1 from Aspergillus oryzae was cloned using a synthetic oligonucleotide probe. The cloned gene (designated rntA) encoded functional RNase T1, since an A. oryzae transformant with multiple copies of the rntA gene showed higher RNase T1 activity (over 200 times) than a transformant with a vector. A cDNA was cloned by reverse transcription polymerase chain reaction (RT-PCR) with primers corresponding to the 5' terminus and 3' terminus of the reading frame of the rntA gene. Nucleotide sequencing analysis of both DNAs found that RNase T1 had a prepro-sequence consisting of 26 amino acids and the rntA gene had only one intron (114 bp) in the region encoding the signal sequence. The A. oryzae transformant with cDNA controlled by the amyB promoter also showed higher activity (over 300 times), indicating that the cloned cDNA encoded functional RNase T1. On the other hand, the Saccharomyces cerevisiae transformant with cDNA controlled by the GAL1 promoter could not grow on a medium containing galactose. These results suggests that A. oryzae may have a protection mechanism from RNase T1.
利用合成寡核苷酸探针克隆了来自米曲霉的编码核糖核酸酶(RNase)T1的基因组DNA。克隆的基因(命名为rntA)编码功能性RNase T1,因为携带多个rntA基因拷贝的米曲霉转化体显示出比携带载体的转化体更高的RNase T1活性(超过200倍)。通过逆转录聚合酶链反应(RT-PCR),使用与rntA基因阅读框5'末端和3'末端相对应的引物克隆了cDNA。对这两种DNA的核苷酸序列分析发现,RNase T1具有由26个氨基酸组成的前原序列,并且rntA基因在编码信号序列的区域中只有一个内含子(114 bp)。由amyB启动子控制的cDNA的米曲霉转化体也显示出更高的活性(超过300倍),表明克隆的cDNA编码功能性RNase T1。另一方面,由GAL1启动子控制的cDNA的酿酒酵母转化体不能在含有半乳糖的培养基上生长。这些结果表明米曲霉可能具有针对RNase T1的保护机制。