Fromm H, Edelman M, Koller B, Goloubinoff P, Galun E
Nucleic Acids Res. 1986 Jan 24;14(2):883-98. doi: 10.1093/nar/14.2.883.
A 2.9 kbp region from within the inverted repeat of Nicotiana chloroplast DNA hybridized with a chloroplast DNA fragment from Euglena containing the complete rps12 gene coding for ribosomal protein S12. Nucleotide sequencing within this region revealed the existance of two rps12 coding stretches interrupted by 540 bp having class II intron structure. Joining and decoding the exon regions produced a sequence of 85 amino acids colinear and 81% homologous to the S12 protein of Euglena chloroplasts and E. coli, starting from amino acid residue 38 to the stop codon. Immediately upstream of codon 38, conserved intron sequences were located. However, the 5' 37 codon of Nicotiana chloroplast rps12 could not be identified by electron microscopy of RNA-DNA hybrids within a DNA region extending 4000 bp upstream of codon 38, nor by computer search of a completely sequenced region extending for more than 9000 bp upstream of this codon. In E. coli, alteration in rps12 codons 42 or 87 causes streptomycin resistance. However, the nucleotide sequence of the identified rps12 exons in two Nicotiana chloroplast mutants resistant to streptomycin were found to be identical to that of wild type.
烟草叶绿体DNA反向重复序列中的一个2.9千碱基对区域,与来自眼虫属的一个叶绿体DNA片段杂交,该片段含有编码核糖体蛋白S12的完整rps12基因。该区域内的核苷酸测序显示存在两个rps12编码区段,被具有II类内含子结构的540碱基对隔开。连接并解读外显子区域产生了一个85个氨基酸的序列,与眼虫属叶绿体和大肠杆菌的S12蛋白共线且同源性为81%,从氨基酸残基38到终止密码子。在密码子38的紧邻上游,定位到了保守的内含子序列。然而,通过对密码子38上游4000碱基对的DNA区域内的RNA-DNA杂交体进行电子显微镜观察,以及通过对该密码子上游延伸超过9000碱基对的完全测序区域进行计算机搜索,均未能鉴定出烟草叶绿体rps12的5'端37个密码子。在大肠杆菌中,rps12密码子42或87的改变会导致链霉素抗性。然而,在两个对链霉素抗性的烟草叶绿体突变体中,所鉴定的rps12外显子的核苷酸序列与野生型相同。