Berg B L, Baron C, Stewart V
Section of Microbiology, Cornell University, Ithaca, New York 14853-8101.
J Biol Chem. 1991 Nov 25;266(33):22386-91.
fdnG, encoding the selenopeptide of Escherichia coli formate dehydrogenase-N, contains an in-frame opal (UGA) codon at amino acid position 196 that directs selenocysteine incorporation. We have identified sequences that contribute to the mRNA context required for decoding this UGA as selenocysteine. We identified a potential stem-loop structure immediately downstream of UGA196 that is comparable in size and structure to a stem-loop predicted to form in fdhF, which encodes the selenopeptide of E. coli formate dehydrogenase-H. Mutational analysis of the fdnG stem-loop structure suggests that it is critical for decoding UGA196 as selenocysteine. Our data indicate that both stability and specific nucleotide sequences of the stem-loop likely contribute to the appropriate mRNA context for selenocysteine incorporation into the fdnG gene product.
编码大肠杆菌甲酸脱氢酶 -N 的硒代肽的 fdnG,在氨基酸位置 196 处含有一个框内乳白(UGA)密码子,该密码子指导硒代半胱氨酸的掺入。我们已经鉴定出有助于将该 UGA 解码为硒代半胱氨酸所需的 mRNA 上下文的序列。我们在 UGA196 下游立即鉴定出一个潜在的茎环结构,其大小和结构与预测在 fdhF 中形成的茎环相当,fdhF 编码大肠杆菌甲酸脱氢酶 -H 的硒代肽。对 fdnG 茎环结构的突变分析表明,它对于将 UGA196 解码为硒代半胱氨酸至关重要。我们的数据表明,茎环的稳定性和特定核苷酸序列可能都有助于为硒代半胱氨酸掺入 fdnG 基因产物提供合适的 mRNA 上下文。