DEVELOPMENTAL CONTROL OF INTRODUCED GENES IN RODENTS
DEVELOPMENTAL CONTROL OF INTRODUCED GENES IN RODENTS
批准号:
2092059
负责人:
SUSAN R ROSS
金额:
$16.26万
依托单位国家:
美国
项目类别:
财政年份:
1987
资助国家:
美国
项目状态:
已结题
起止时间:
1987-05-15 至 1997-02-28
关键词:
DNA binding protein RNase protection assay Retroviridae disease SDS polyacrylamide gel electrophoresis antibody formation breast neoplasms embryo /fetus gene expression genetic manipulation genetic mapping genetic transcription genetically modified animals laboratory mouse laboratory rabbit mammary gland mammary tumor virus microinjections molecular cloning northern blottings nucleic acid repetitive sequence nucleic acid sequence oncogenes oncoproteins open reading frames site directed mutagenesis southern blotting tissue /cell culture transcription factor transfection viral carcinogenesis virus DNA virus genetics
中文摘要
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英文摘要
The objective of the experiments described in this proposal is to dissect
the molecular mechanisms which affect the developmental regulation of
expression of the endogenous murine retrovirus, mouse mammary tumor Virus
(MTV) and limit the induction of mammary carcinomas by this virus to the
mammary gland. An additional goal is to achieve an understanding of the
genetic factors that determine whether mice are susceptible to MTV-induced
mammary tumors and the role of the immune system in this process. To
achieve these goals, a combination of molecular cloning techniques, tissue
culture transfection studies and transgenic mice will be used to
characterize the DNA sequences within the long terminal repeat (LTR) of MTV
that direct expression of the virus to the mammary gland. Additionally,
the transcription factors that Interact with these DNA sequences will be
cloned and used to study expression of these factors in the developing
mammary gland of different mouse strains and in mammary tumors. Lastly,
the role of the MTV LTR open reading frame (ORF) protein, which influences
the T cell repertoire in mice, will be assessed, In both the virus life
cycle and in the susceptibility of different strains of mice to MTV-induced
carcinomas. The experiments outlined in this proposal will allow us to
begin to dissect the contributions of genetic background to the tumorigenic
process initiated by MTV and the role of the immune system in responding to
viral infection and tumorigenesis. By extension, these experiments will
also increase our understanding of the role of these different components
in human breast cancer.
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