Interferon induction of (2′–5′) oligoisoadenylate synthetase in diploid and trisomy 21 human fibroblasts: Relation to dosage of the interferon receptor gene (IRFC)

Trisomy 21 human fibroblasts are more sensitive to human interferon-alpha (IFN-alpha) than are diploid controls, consistent with the location of the gene (IFRC) which codes for the IFN-alpha receptor on chromosome 21. When compared in the antiviral assay, the difference in sensitivity is five- to tenfold, much greater than the 50% difference in IFRC gene dosage. An understanding of the mechanism by which this amplification of gene dosage occurs is relevant to the specific pathology of Down's syndrome and as a model system for studying the pathogenic effects of chromosomal aneuploidy. The enzyme (2'-5') oligoisoadenylate synthetase (2-5A synthetase), which is believed to be central to the interferon-induced antiviral response, is induced 50% more in trisomy 21 fibroblasts than in diploid controls. Thus the amplification in response occurs subsequent to the binding of IFN-alpha to its receptor and the triggering of the first set of intracellular events, the latter exemplified by the induction of 2-5A synthetase. Similar results were obtained with IFN-gamma, consistent with other evidence which indicates that a gene coding for a separate IFN-gamma receptor is also located on chromosome 21.     

Polypeptide induction by recombinant human IFN-gamma

Partially purified natural human IFN-gamma has been shown to induce the synthesis of a set of unique polypeptides that are not induced by comparable amounts of IFN-alpha and IFN-beta. In addition, a set of polypeptides is induced in common by all three IFNs. The present study utilized a pure recombinant IFN-gamma and a monoclonal antibody against IFN-gamma to investigate whether the unique polypeptide-inducing properties previously reported are due to IFN-gamma itself. With the possible exception of two polypeptides, the results demonstrate conclusively that IFN-gamma is the sole molecular species responsible for the induction of all polypeptides, including those whose induction pattern is unique to IFN-gamma. Very high doses of IFN-alpha and IFN-beta induce some of the latter set of polypeptides to a limited extent. Thus the differential effects of IFN-gamma compared to IFN-alpha and IFN-beta are, in part, quantitative rather than qualitative in nature.     

Enhanced ultraviolet radiation can terminate sexual reproduction in the broadcasting coral species Acropora cervicornis Lamarck

The effects of enhanced ultraviolet radiation (280-400 nm: UVR) on the fecundity of Acropora cervicornis were measured in field-transplanted colonies from 20 m to 1 m depth and vice versa at La Parguera, Puerto Rico. Fecundity was estimated from histological sections made from tissue samples obtained at different time intervals during the experimental period (March - August 2003). All colonies transplanted from 20 m to 1 m showed a 100% reduction in gonads per mesentery per polyp one month after transplantation, while those transplanted from 1 m to 20 m did not show any significant reduction in fecundity throughout the experimental period. The latter colonies did show however, a delay in the spawning times by releasing their gamete bundles approximately two-three weeks after the controls at 1 m and two months after the controls at 20 m suggesting an induced response as a consequence of changes in their daily light cycle due to less radiation (PAR and UVR) available at 20 m compared to 1 m. Control colonies at 20 m spawned after the full moon of June 2003, while the controls at 1 m spawned 5-6 days after the full moon of July 2003. While a possible reabsorption of the gametes occurred in A. cervicornis colonies transplanted from 20 m to 1 m, the expulsion of these gametes due to the sudden stress caused by the transplantation is not discarded. The results suggest that sudden increases in UVR can completely stop sexual reproduction in ramose broadcasting coral species, which in turn can affect the dominance of the species and the composition and structure of shallow reef environments.