TELOMERASES AND TELOMERASE MOLECULAR BIOLOGY
端粒酶和端粒酶分子生物学
基本信息
- 批准号:6269711
- 负责人:
- 金额:$ 9.58万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-09-30 至 1999-09-29
- 项目状态:已结题
- 来源:
- 关键词:HeLa cells RNA cell line cooperative study enzyme inhibitors enzyme reconstitution gene expression genetic mapping hybrid cells molecular cloning nucleic acid repetitive sequence nucleic acid sequence oligonucleotides polymerase chain reaction protein structure function site directed mutagenesis telomerase telomere
项目摘要
Telomeres have a G-rich repeated DNA sequence that maintains chromosome
end stability. Telomerase is a reverse transcriptase-like
ribonucleoprotein that maintains the telomere sequence. Telomerase is
expressed in the majority of tumor cells but not in normal cells.
Telomerase and telomeres are ideal tumor-specific targets for anti-cancer
therapeutic strategies. Our preliminary studies show the discovery of the
first telomerase inhibitors. Our studies also show that telomerase
inhibitors induce telomere shortening, chromosome end fusion, and
eventually cell death. Cells have shown the ability to adapt to telomerase
inhibition.
The goals of this proposal are to l) elucidate the molecular structure of
telomerase and provide a more defined target for our anti-cancer
strategies, and 2) determine the mechanism(s) of cellular adaptation to
telomerase inhibitors. These goals will be accomplished by mapping and
cloning the genes for the telomerase proteins and RNA template. Through
our collaboration with Program l, purified telomerase will be used as a
source of purified telomerase RNA for cloning. Somatic cell genetics will
be used to map the telomerase activity. The new technique of Differential
Display will be used to detect mRNAs expressed in posttelomerase-activated
cells that are not expressed in pre-telomerase activated cells. The
mapping will be coordinated with the isolation of candidate cDNA clones
for the proteins and RNA to accelerate the identification of legitimate
clones. The cDNA clones of the RNA will be screened for appropriate
template sequence, secondary structure, and ability to direct in vitro and
in vivo telomerase activity. The cDNAs for telomerase proteins will be
expressed for production of antibodies.
The antibodies and DNA clones will serve as probes for use in studies of
telomerase expression in Program 3 and in tumor specimens from Program 4.
The data from these studies will be used by Program 2 for structure
modeling and specific drug design. Potential telomerase inhibitors, such
as anti RNA oligonucleotides will be studied by Program l. The mechanism
of adaptation to telomerase inhibitors will also be studied. Hypotheses
concerning drug metabolism, telomerase up-regulation and telomerase
specificity will be tested.
端粒有一个富含g的重复DNA序列来维持染色体
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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BRAD E. WINDLE其他文献
BRAD E. WINDLE的其他文献
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{{ truncateString('BRAD E. WINDLE', 18)}}的其他基金
Novel Structures of the Human Papilloma Virus Genome in HNSCC
HNSCC 中人乳头瘤病毒基因组的新结构
- 批准号:
9332364 - 财政年份:2016
- 资助金额:
$ 9.58万 - 项目类别:
Novel Structures of the Human Papilloma Virus Genome in HNSCC
HNSCC 中人乳头瘤病毒基因组的新结构
- 批准号:
9166448 - 财政年份:2016
- 资助金额:
$ 9.58万 - 项目类别:
HTERT EXPRESSION AS A MARKER FOR EARLY CANCER DETECTION
HTERT 表达作为早期癌症检测的标志
- 批准号:
6378217 - 财政年份:2000
- 资助金额:
$ 9.58万 - 项目类别:
HTERT EXPRESSION AS A MARKER FOR EARLY CANCER DETECTION
HTERT 表达作为早期癌症检测的标志
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6317199 - 财政年份:2000
- 资助金额:
$ 9.58万 - 项目类别:
EXTRACHROMOSOMAL DNA IN PATIENTS' OVARIAN CANCERS
卵巢癌患者的染色体外 DNA
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2099242 - 财政年份:1994
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$ 9.58万 - 项目类别:
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2209210 - 财政年份:1993
- 资助金额:
$ 9.58万 - 项目类别:
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