The sister chromatid exchange (SCE) technique has been proposed as a mutagenic assay in genetic toxicology testing. The complete and successful application of this procedure is currently not possible because the underlying mechanism(s) and biological consequences of SCE are not known. We propose to use the chick embryo to study the nature of mutagen-induced SCE and the effects of such in the hemopoietic and immune systems at pre- and post-natal stages. In addition, this research contributes to the development of an in vivo assay for detecting mutagens and their long-range effects resulting from prenatal exposure. Chick embryos will be exposed to selected mutagen/non-mutagen pairs to determine the specificity of the SCE response and its use in discriminating weak from strong mutagens. Chick embryos at early and late developmental ages will be exposed to direct and indirect-acting chemical mutagens to test the hypothesis that with the progressive growth and differentiation of tissues the extent of metabolic toxification/detoxification increases. Thus, the extent of mutagenesis by promutagens increases while the reverse is true for direct-acting mutagens. The protocol of exposing embryos at different ages to promutagens will also be used for the assay of effects on differentiation and functioning of white and red blood cells. Growth rate, immune functioning, and production of tumors will be studied in chickens surviving the prenatal exposure to mutagen/non-mutagen pairs. The frequency of SCE induced by the chemicals will be studied in parallel embryos injected with BrdU for labeling chromosomal DNA. The degree and type of malformations induced following prenatal exposure will be correlated with the frequency of SCE. If SCE is a manifestation of damage to the DNA that leads to point mutations, we expect to see some deleterious phenotypic effects particularly if the level of SCE is high in every cell. Our research also contributes to knowledge of the action of flame retardants, mycotoxins, and dyes in a developing system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES003499-09
Application #
3250825
Study Section
Chemical Pathology Study Section (CPA)
Project Start
1981-05-01
Project End
1993-04-30
Budget Start
1990-05-01
Budget End
1991-04-30
Support Year
9
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
Schools of Earth Sciences/Natur
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Muscarella, D E; Rachlinski, M K; Sotiriadis, J et al. (1998) Contribution of gene-specific lesions, DNA-replication-associated damage, and subsequent transcriptional inhibition in topoisomerase inhibitor-mediated apoptosis in lymphoma cells. Exp Cell Res 238:155-67
Muscarella, D E; Bloom, S E (1997) Involvement of gene-specific DNA damage and apoptosis in the differential toxicity of mitomycin C analogs towards B-lineage versus T-lineage lymphoma cells. Biochem Pharmacol 53:811-22
Hemendinger, R A; Bloom, S E (1996) Selective mitomycin C and cyclophosphamide induction of apoptosis in differentiating B lymphocytes compared to T lymphocytes in vivo. Immunopharmacology 35:71-82
Miller, M M; Goto, R M; Taylor Jr, R L et al. (1996) Assignment of Rfp-Y to the chicken major histocompatibility complex/NOR microchromosome and evidence for high-frequency recombination associated with the nucleolar organizer region. Proc Natl Acad Sci U S A 93:3958-62
Lorr, N A; Sinclair, J F; Sinclair, P R et al. (1994) Detection and localization of 3,3',4,4'-tetrachlorobiphenyl-induced P4501A protein in avian primary immune tissues. Int J Immunopharmacol 16:875-85
Moore, F R; Calnek, B W; Bloom, S E (1994) Cytogenetic studies of cell lines derived from Marek's disease virus-induced local lesions. Avian Dis 38:797-9
Moore, F R; Schat, K A; Hutchison, N et al. (1993) Consistent chromosomal aberration in cell lines transformed with Marek's disease herpesvirus: evidence of genomic DNA amplification. Int J Cancer 54:685-92
Potchinsky, M B; Bloom, S E (1993) Selective aflatoxin B1-induced sister chromatid exchanges and cytotoxicity in differentiating B and T lymphocytes in vivo. Environ Mol Mutagen 21:87-94
Lorr, N A; Golemboski, K A; Hemendinger, R A et al. (1992) Distribution and inducibility of a P450I activity in cellular components of the avian immune system. Arch Toxicol 66:560-6
Delany, M E; Dietert, R R; Bloom, S E (1992) The effects of MHC chromosome dosage on bursal B-cell subpopulations in embryonic and neonatal chickens. Dev Comp Immunol 16:313-27

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