Two fragments cloned from purified human satellite III DNA do not cross-react with each other. One fragment, for which a partial sequence is reported, hybridises to satellite II as well as III and is shown to originate on chromosome 1. The other cloned fragment originates from the Y chromosome. This fragment has undergone considerable changes in size when cloned in lambda gt WES lambda B. Human satellite III is shown to consist of a number of non-cross-reacting sequences which nevertheless are related by the presence of closely spaced Hin F1 sites.

No abstract

A cosmid library was prepared from a partial BamHJ digest of total DNA from Bacillus sphaericus SSII-1. Two hundred fifty Escherichia coli clones were screened for toxicity against larvae of the mosquito Culex quinquefasciatus. One toxic clone, designated pKF2, was chosen for further study. Two toxic subclones, designated pXP33 and pXP34, obtained by ligating PstI-derived fragments of pKF2 into pUC18, contained the same 3.8-kb fragment, but in opposite orientations. Sequence analysis revealed the presence of an open reading frame corresponding to a 100-kDa protein and the 3' end of a further open reading frame having significant homology to open reading frames of transposons TnSOl and Tn2l. The sequence of the SSII-1 toxin was compared with those of known toxins and was found to show regional homology to those of ADPribosyltransferase toxins. The distribution of the toxin gene among other B. sphaericus strains was examined.Bacillus sphaericus is an aerobic spore-forming Bacillus species, several strains of which are pathogenic for mosquito larvae (13). B. sphaericus SSII-1 was isolated in 1973 from infected mosquito larvae collected in India (36). This strain was considerably more toxic than the other B. sphaericus strains known at that time. Early studies indicated that the toxin was retained within or attached to the bacterial cells and that the toxic activity was markedly unstable. Storage of cells under refrigeration or heating at 80°C resulted in the loss of activity. Toxin production occurred predominantly in the vegetative phase of growth before the onset of sporulation (27,29).Further studies on B. sphaericus SSII-1 declined rapidly with the discovery of strains, such as 1593 (36a), 2362 (40), and 2297 (41), which had higher toxicities. In contrast to strain SSII-1, these strains develop relatively stable, high toxicity at the onset of sporulation (7). To date, two types of toxin have been characterized in the highly toxic strains: a pair of proteins of 51.4 and 41.9 kDa associated with the parasporal crystal (3,5,19) and a toxin of 110 kDa related to a 125-kDa surface layer protein (5, 6). Genes encoding the 51.4-and 41.9-kDa proteins were shown to be absent from strain SSII-i (4). In the same study, Baumann et al. showed that sequences inserted in their group C clones were also absent from strain SSII-1. The group C clones were later shown to contain sequences corresponding to the gene encoding the 125-kDa protein (6). Davidson (12) Construction of the cosmid library. To prepare total genomic DNA from B. sphaericus SSII-1, we lysed cells in the presence of 1% sodium dodecyl sulfate and 0.1 mg of proteinase K per ml. DNA was purified from the lysate by the method of Ausubel et al. (2). In brief, hexadecyltrimethyl ammonium bromide was added, and the mixture was incubated at 65°C for 20 min prior to extraction with chloroformisoamyl alcohol. DNA was precipitated with ethanol from the aqueous phase and purified by banding on a cesium chloride gradient coqtaining ethidium bromide. DNA was partially digest...

No abstract