The amino acid sequence of the Dsg protein is 50%o identical to that of translation initiation factor IF3 of Escherichia coli, the product of its infC gene. dsg mutants are able to initiate the developmental process, but their development goes awry when the cells have formed loose asymmetric aggregates, at about 6 to 10 h. These mutants are unable to transcribe a particular set of developmentally regulated genes (3). The dsg mutation also affects the cells during vegetative growth. Mutants form compact, heaped, smooth-edged colonies, unlike the flat, spreading wild-type colonies. These mutants are also defective in the phase variation of colony color. In the accompanying paper (5), we describe the sequence of the dsg gene, which contains a missense mutation in dsg mutants. The amino acid sequence of Dsg is 50% and 51% identical to that of translation initiation factor IF3 of both Escherichia coli and Bacillus stearothermophilus, respectively. We also show that like IF3, Dsg begins with a unique initiation codon and contains conserved residues which are critical for the function of IF3. The Dsg protein extends 66 more amino acids to its C terminus than the IF3 proteins of E. coli, other enteric bacteria, and B. stearothermophilus.An important role of IF3 in translation initiation is to help the ribosome select the initiation codon on the mRNA. Thus, IF3 ensures the fidelity of translation by preventing initiation at an incorrect location in the message or in the wrong reading frame (12,13,26 codon. The IF3 protein, which is associated with the 30S ribosomal subunit during initiation, inspects the codons near the Shine-Dalgarno site for one which will pair correctly with the anticodon on the initiator tRNA, fMet-tRNA et, which is also associated with the 30S subunit. When the proper initiation codon is located, the 50S ribosomal subunit joins the 30S initiation complex to form the 70S ribosome, and the initiation factors are released (8).The infC gene, which encodes IF3 in E. coli, begins with the atypical AUU initiation codon (21). Recent work shows that IF3 selects against initiation at AUU codons and for initiation at AUG, GUG, and UUG codons, the typical initiators. In fact, this atypical AUU initiation codon is involved in the translational autoregulation of infC expression (2,9,26). When IF3 levels are high, the mRNA encoding infC is not translated because IF3 does not recognize AUU for the initiation of translation. However, when IF3 levels are low, the infC message is translated because, in the absence of IF3, the ribosome shows low selectivity for the typical initiation codons. Translation of infC from AUU continues until the levels of IF3 are high enough to restrict translation from an AUU initiation codon, thus regulating the cellular level of the IF3 protein according to its function (1, 2, 9).In this work, we show that Dsg reacts with anti-IF3 serum. Using anti-Dsg antibodies, we show that Dsg is present at constant levels at all times during vegetative growth and development, as would be expected of ...