The in vitro synthesis and characteristics of ribosomal RNA in imaginal discs of Drosophila melanogaster

Summary Late third instar imaginal discs of Drosophila melanogaster cultured in vitro in Robb's tissue culture medium synthesize 38S, 28S and 18S ribosomal RNAs which are qualitatively indistinguishable from their in vivo synthesized counterparts (Fig. 1). As found in other insect systems, the 38S molecule appears to be the precursor for both the 28S and 18S rRNAs (Figs. 2, 3 and 4). The 28S rRNA and a portion of the 38S pre-rRNA shift in sedimentation value upon exposure to heat or dimethylsulfoxide (Figs. 5 and 8). Studies of the thermal denaturations of these molecules (Figs. 6, 7 and 9) indicate the existence of a single class of 28S rRNA, but three classes of 38S pre-rRNAs. The addition of -ecdysone to the in vitro culture medium stimulates the net amount of rRNA synthesized, increases the rate of processing of the 38S precursor and increases the relative amount of 18S material produced (Figs. 10 and 12).This work was supported in part by grants from the National Science Foundation (GB-8176) and from the Atomic Energy Commission (AT-04-3-34).Predoctoral Trainees, PHS Training Grant No. 2-Tl-GM367 from Research Training Grants Branch, National Institute of General Medical Sciences.1 For purposes of simplification we shall refer to the rRNA molecules of D. melanogaster as being 38S, 30S, 28S and 18S; however, it should be noted that these values are approximate (see Hastings and Kirby, 1966; Greenberg, 1969; Tartof and Perry, 1970).     

Hydrolysis of bradykinin and its higher homologues by angiotensin-converting enzyme (Short Communication)

The hydrolysis of bradykinin and its higher homologues by angiotensin-converting enzyme has been investigated by using an automated ninhydrin technique. The results show an inverse relationship of hydrolysis rate with size and charge of the peptide, which parallels the inactivation in the pulmonary circulation and offers an explanation for the selectivity of metabolism of these kinins by the lungs.     

Hominid divergence and speech evolution

Hominids evolved from a population which diverged from other hominoids during the Mio-Pliocene. This population was perhaps forced by ecological conditions and competitive exclusion to rely more on tools, gathering, hunting, vocal communication and memory, under whose mutually positively reinforcing effects the hominids diverged. The ape ancestors may have been forced into the forests (or they may have forced hominids onto the savanna), while hominids adapted to a plains, hunting econiche.Speech was selected for because verbal symbols served as retrieval cues for a large number of complex concepts and were transmissible, and thus could be used to influence food-getting and other behavior by the social group.Speech is dependent on three inherited entities: (1) anatomical and neurological adaptations which allow vocalization of a wide range of phonemes in rapid succession and which allow for (2) duality of patterning, thereby promoting a large number of words, and (3) encoding, which greatly increases the rate at which verbal information transfer can occur. Speech may have evolved through small hominid groups using progressively more phonemes in an increasingly blended manner, with encoding subsequently being selected for. Neandertals apparently could not encode speech and could speak only a restricted range of phonemes. Their expanded cranial capacity may have been selected for to store ambiguous and slowly transmitted verbal data.     

Some functional properties of hemoglobin Leiden

Hemoglobin Leiden, a human mutant that contains a deletion of a glutamic residue at position 6 or 7 (A3 or A4) of the #x03B2; chains, has a slightly higher oxygen affinity in 0.1 M Phosphate, a normal Bohr effect but an abnormal response to 2,3 diphosphoglycerate and inositol hexaphosphate. Hb Leiden participates to the same extent as does Hb A in gelation with deoxy Hb S.     

Degradation of polysaccharides containing uronic acid residues

A method for the selective degradation of polysaccharides containing uronic acid residues is described. It involves methylation of hydroxyl and carboxyl groups, base-catalysed elimination, and mild hydrolysis with acid. The degraded product is etherified with trideuteriomethyl or ethyl groups and hydrolysed, and the resulting mixture of etherified sugars is analysed, as the alditol acetates, by g.l.c.—m.s. Comparison of this analysis with the methylation analysis of the original polysaccharide gives information on the nature of the sugar residues on either side of the uronic acid residue.     

Preparation and some properties of stable and carbon-14 and tritium-labeled short-chain aliphatic hydroxamic acids

A simple and safe procedure has been described for the preparation of short-chain aliphatic hydroxamic acids in quantities as large as 1 mole and as small as 0.01 mole. The procedure is equally suitable for the preparation of isotopically labeled hydroxamates, as has been demonstrated in the case of 1-¹⁴C-acetohydroxamic acid and ³H-acetohydroxamic acid. Some physical and chemical characteristics, including infrared spectra of formo-, aceto-, propiono-, and isobutyro-hydroxamic acids prepared by this method have been described.