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A new osmotically inducible gene in Escherichia coli, osmY, was induced 8- to 10-fold by hyperosmotic stress and 2- to 3-fold by growth in complex medium. The osmY gene product is a periplasmic protein which migrates with an apparent molecular mass of 22 kDa on sodium dodecyl sulfate-polyacrylamide gels. A genetic fusion to osmY was mapped to 99.3 min on the E. coli chromosome. The gene was cloned and sequenced, and an open reading frame was identified. The open reading frame encoded a precursor protein with a calculated molecular weight of 21,090 and a mature protein of 18,150 following signal peptide cleavage. Sequencing of the periplasmic OsmY protein confirmed the open reading frame and defined the signal peptide cleavage site as Ala-Glu. A mutation caused by the osmY::TnphoA genetic fusion resulted in slightly increased sensitivity to hyperosmotic stress.

Finewooled Rambouillet range ewes were used in a study to determine the feasibility of using a progesterone ear implant to synchronize estrus. In addition, some of the ewes were further treated with injections of follicle stimulating hormone-pituitary (FSH-P) to induce superovulation. Five days following estrus detection and breeding, FSH-P-treated ewes were laparotomized and surgically flushed to recover embryos. The number of corpora lutea (CL), the total number of embryos and the number of transferable embryos recovered were recorded along with the number and size of follicles present on both ovaries. Ewes synchronized as recipients were laparotomized for surgical transfer of embryos 5 d following estrus. The number of CL and follicles were recorded. Response to superovulation by FSH-P did not differ (P>0.05) between age groups of ewes when the number of CL present was counted. However, the total number of embryos flushed and good embryos was lower (P<0.05) among the oldest (7 yr) ewes. The number of follicles present showed little variation between age groups. Recipient ewes (No FSH-P) were similar in the number of CL with 6-yr-old ewes, having fewer (P>0.05) CL, than 3-, 4- or 7-yr-old ewes. Only slight variation was boserved in the number of follicles in recipient ewes. Among donor ewes receiving FSH-P in addition to Synchro-Mate B, 71% were detected in estrus within 48 h of implant removal vs 55% of the recipients.

To determine the role of the HSV-1 genome structure and environment on the regulation of gene expression, we constructed recombinant viruses containing a heterologous gene inserted into either the immediate early ICPO or late glycoprotein C (gC) genes of HSV-1. The heterologous gene consisted of the SV40 early promoter (without enhancer sequences) linked to the coding sequences for the bacterial chloramphenicol acetyl transferase (CAT). The expression of CAT was examined in Vero cells infected with either virus (named ICP0-CAT and Sph 6). For both recombinants, expression of CAT was not dependent upon prior viral protein synthesis. The kinetics of expression of CAT-specific mRNA resembled that of the HSV-1 genes into which CAT was inserted. Primer extension analysis revealed that the SV40 promoter is recognized and used when placed in cis in two different HSV-1 genome locations, and Northern hybridization experiments confirmed that the heterologous gene was expressed in the absence of prior viral protein synthesis. Therefore, this gene was not regulated as strictly as an HSV-1 gene, but was influenced by the environment into which it was placed, presumably by factors that are present when the normal viral gene is on.