Sacerdot C, Vachon G, Laalami S, Morel-Deville F, Cenatiempo Y, Grunberg-Manago M
Institut de Biologie de Physico-Chimique, URA CNRS 1139, Paris, France.
J Mol Biol. 1992 May 5;225(1):67-80. doi: 10.1016/0022-2836(92)91026-l.
The gene infB codes for two forms of translational initiation factor IF2; IF2 alpha (97,300 Da) and IF2 beta (79,700 Da). IF2 beta arises from an independent translational event on a GUG codon located 471 bases downstream from IF2 alpha start codon. By site-directed mutagenesis we constructed six different mutations of this GUG codon. In all cases, IF2 beta synthesis was variably affected by the mutations but not abolished. We show that the residual expression of IF2 beta results from translational initiation on an AUG codon located 21 bases downstream from the mutated GUG. Furthermore, two forms of IF2 beta have been separated by fast protein liquid chromatography and the determination of their N-terminal sequences indicated that they resulted from two internal initiation events, one occurring on the previously identified GUG start codon, the other on the AUG codon immediately downstream. We conclude that two forms of IF2 beta exist in the cell, which differ by seven aminoacid residues at their N terminus. Only by mutating both IF2 beta start codons could we construct plasmids that express only IF2 alpha. A plasmid expressing only IF2 beta was obtained by deletion of the proximal region of the infB gene. Using a strain that carries a null mutation in the chromosomal copy of infB and a functional copy of the same gene on a thermosensitive lysogenic lambda phage, we could cure the lambda phage when the plasmids expressing only one form of IF2 were supplied in trans. We found that each one of the two forms of IF2, at near physiological levels, can support growth of Escherichia coli, but that growth is retarded at 37 degrees C. This result shows that both forms of IF2 are required for maximal growth of the cell and suggests that they have acquired some specialized but not essential function.
基因infB编码两种形式的翻译起始因子IF2;IF2α(97300道尔顿)和IF2β(79700道尔顿)。IF2β源自位于IF2α起始密码子下游471个碱基处的GUG密码子上的独立翻译事件。通过定点诱变,我们构建了该GUG密码子的六种不同突变。在所有情况下,IF2β的合成均受到突变的不同程度影响,但未被消除。我们表明,IF2β的残留表达是由位于突变的GUG下游21个碱基处的AUG密码子上的翻译起始导致的。此外,通过快速蛋白质液相色谱法分离出了两种形式的IF2β,其N端序列的测定表明它们源自两个内部起始事件,一个发生在先前确定的GUG起始密码子上,另一个发生在紧邻的AUG密码子上。我们得出结论,细胞中存在两种形式的IF2β,它们在N端相差七个氨基酸残基。只有通过突变两个IF2β起始密码子,我们才能构建仅表达IF2α的质粒。通过缺失infB基因的近端区域获得了仅表达IF2β的质粒。使用在infB的染色体拷贝中携带无效突变且在温度敏感的溶原性λ噬菌体上具有相同基因功能拷贝的菌株,当提供反式表达仅一种形式IF2的质粒时,我们可以治愈λ噬菌体。我们发现,两种形式的IF2中的每一种在接近生理水平时都可以支持大肠杆菌的生长,但在37℃时生长会受到抑制。该结果表明,两种形式的IF2都是细胞最大生长所必需的,并表明它们已获得了一些特殊但非必需的功能。