Modulator of Apoptosis 1 (MOAP-1) Is a Tumor Suppressor Protein Linked to the RASSF1A Protein

Modulator of apoptosis 1 (MOAP-1) is a BH3-like protein that plays key roles in cell death or apoptosis. It is an integral partner to the tumor suppressor protein, Ras association domain family 1A (RASSF1A), and functions to activate the Bcl-2 family pro-apoptotic protein Bax. Although RASSF1A is now considered a bona fide tumor suppressor protein, the role of MOAP-1 as a tumor suppressor protein has yet to be determined. In this study, we present several lines of evidence from cancer databases, immunoblotting of cancer cells, proliferation, and xenograft assays as well as DNA microarray analysis to demonstrate the role of MOAP-1 as a tumor suppressor protein. Frequent loss of MOAP-1 expression, in at least some cancers, appears to be attributed to mRNA down-regulation and the rapid proteasomal degradation of MOAP-1 that could be reversed utilizing the proteasome inhibitor MG132. Overexpression of MOAP-1 in several cancer cell lines resulted in reduced tumorigenesis and up-regulation of genes involved in cancer regulatory pathways that include apoptosis (p53, Fas, and MST1), DNA damage control (poly(ADP)-ribose polymerase and ataxia telangiectasia mutated), those within the cell metabolism (IR-α, IR-β, and AMP-activated protein kinase), and a stabilizing effect on microtubules. The loss of RASSF1A (an upstream regulator of MOAP-1) is one of the earliest detectable epigenetically silenced tumor suppressor proteins in cancer, and we speculate that the additional loss of function of MOAP-1 may be a second hit to functionally compromise the RASSF1A/MOAP-1 death receptor-dependent pathway and drive tumorigenesis.     

Reshaping the Ecology of Invading Populations of Hemlock Woolly Adelgid, Adelges tsugae (Homoptera: Adelgidae), in Eastern North America

Hemlock woolly adelgid, Adelges tsugae Annand (Homoptera: Adelgidae), is native to Japan where it is an innocuous inhabitant of Tsuga diversifolia Masters and T. sieboldii Carriere throughout their natural growing areas. Native adelgid populations are regulated by host resistance and natural enemies, in particular the oribatid mite, Diapterobates humeralis (Hermann) and the coccinellid beetle, Pseudoscymnus tsugae Sasaji and McClure. Invading populations of A. tsugae in western North America on T. heterophylla Sargent and T. mertensiana Carriere are mainly regulated by host resistance. However, invading populations in eastern North America attain damaging levels on T. canadensis (L.) Carriere and T. caroliniana Engelmann and are regulated mainly by weather and negative density-dependent feedback mechanisms related to host deterioration. Although A. tsugae is only passively dispersed by wind, birds, forest-dwelling mammals and humans, it is spreading at an alarming rate and is sufficiently cold hardy to threaten the existence of the two eastern hemlock species throughout their natural ranges. The current hope for suppressing invading populations of hemlock woolly adelgid in eastern North America lies with the exotic predator, P. tsugae. Extensive laboratory studies of the biology and predatory ability of P. tsugae revealed that it feeds on all life stages of its prey, that its multivoltine life cycle is well synchronized with that of the adelgid, and that it has great potential for biological control. We have reared and released nearly 130,000 adults of P. tsugae in forests in Connecticut, New Jersey and Virginia during the past four years. P. tsugae has reproduced, dispersed, overwintered and reduced densities of hemlock woolly adelgid by 47–88% in only five months on release branches at these sites. Current studies are investigating the long-term ability of P. tsugae to regulate invading populations of A. tsugae in eastern North America.     

Cloning and molecular analysis of the finO region from the antibiotic-resistance plasmid R6-5

The cloning of the finO region from the antibiotic-resistance plasmid R6-5 is reported. On the basis of DNA deletion analysis and Tn5 transposon insertional mutagenesis of finO+ chimeric plasmids, finO has been located within the coordinates 94.0-94.85 on the R6-5 map. A 32,000-Da polypeptide (32K), which is encoded within 92.75-94.25R6-5, has been identified and shown not to be associated with the FinO phenotype.     

Primary structure of the human fgr proto-oncogene product p55c-fgr.

Normal human c-fgr cDNA clones were constructed by using normal peripheral blood mononuclear cell mRNA as a template. Nucleotide sequence analysis of two such clones revealed a 1,587-base-pair-long open reading frame which predicted the primary amino acid sequence of the c-fgr translational product. Homology of this protein with the v-fgr translational product stretched from codons 128 to 516, where 32 differences among 388 codons were observed. Sequence similarity with human c-src, c-yes, and fyn translational products began at amino acid position 76 of the predicted c-fgr protein and extended nearly to its C-terminus. In contrast, the stretch of 75 amino acids at the N-terminus demonstrated a greatly reduced degree of relatedness to these same proteins. To verify the deduced amino acid sequence, antibodies were prepared against peptides representing amino- and carboxy-terminal regions of the predicted c-fgr translational product. Both antibodies specifically recognized a 55-kilodalton protein expressed in COS-1 cells transfected with a c-fgr cDNA expression plasmid. Moreover, the same protein was immunoprecipitated from an Epstein-Barr virus-infected Burkitt's lymphoma cell line which expressed c-fgr mRNA but not in its uninfected fgr mRNA-negative counterpart. These findings identified the 55-kilodalton protein as the product of the human fgr protooncogene.     

Lipid analysis of skeletal muscle from pigs susceptible to malignant hyperthermia

Previous studies demonstrated that lipid profiles of humans and pigs susceptible to malignant hyperthermia (MH) differ from those of normal humans and pigs. Lipid extraction techniques retaining in vivo lipid profiles most closely were used in the present study to determine if stimulation of lipolysis by the processes of homogenization or extraction might account for the reported differences in lipid profiles. No differences were observed among three genotypes of British Landrace pigs with respect to cholesterol levels, triglyceride levels, or total lipid phosphorus values of whole muscle (longissimus dorsi). Phospholipid distributions were the same for all three groups. Individual free fatty acids and fatty acids acylated to triglycerides were similar among the genotypes. These results do not support altered lipid profiles in vivo in MH-susceptible swine. Previously used homogenization and extraction procedures most likely affect the lipolytic activity to a different extent in muscle from MH-susceptible pigs and normal pigs.     

Temperature requirements of the chrysanthemum leaf miner,Chromatomyla syngenesiae [Dipt.: Agromyzidae], and its ectoparasitoid,Diglyphus isaea [Hym.: Eulophidae]

The development rate from egg to adult for ♂ and ♀Chromatomyia (Phytomyza) syngenesiae andDiglyphus isaea increased linearly between 19 and 25°C.D. isaea had a faster developmental rate thanC. syngenesiae between 19 and 25°C but therer was no difference at 16°C. FemaleD. isaea required 154.6 D° above the theoretical threshold of 12.80°C and maleD. isaea 152.4 D° above 12.9°C for total development from egg to adult emergence. FemaleC. syngenesiae needed 207.0 D° above 12°C and ♂ and 211.0 D° above 11.6°C for total development.