GERM CELLS--DNA REPAIR, MUTATION, & ENVIRONMENTAL AGENTS
生殖细胞——DNA 修复、突变、
基本信息
- 批准号:6147882
- 负责人:
- 金额:$ 2.59万
- 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 2002-09-29
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION: Germline mutations can impact substantially on human health
by having debilitating effects on ensuing offspring. It is estimated that
5% of liveborn offspring will have a genetic disorder. Of these, 20% are
due to germline de novo mutations. From a genetic perspective, germ cells
are profoundly different from somatic cells because they carry the DNA for
the next generation of the organism, not simply for the next daughter
cell. It seems logical to assume that safeguarding the integrity of germ-
line DNA would provide survival advantages. Notably, testis has the lowest
mutation frequency among tissues in lacI transgenic mice. Thus, it is
reasonable to speculate that multiple safeguarding mechanisms may have
evolved with this tissue type. An approach is presented to test the
hypothesis that modulation of DNA repair pathways that are potentially
important in determining spontaneous mutation frequencies in spermatogenic
cells. First, various DNA repair activities will be assayed in cells at
defined stages of spermatogenesis to identify DNA repair pathways that are
potentially important in determining spontaneous mutation frequencies in
spermatogenic cells. Based on these results, transgenic mice that have
reduced activity in an appropriate pathway(s) will be made doubly
transgenic by crossing with mice carrying the lacI transgene. lacI
mutation frequencies will then be measured for specific spermatogenic cell
types to confirm which DNA repair pathways play a fundamental role in
determining spontaneous mutation frequencies. In the next phase, lacI and
lacZ transgenic male mice will treated with an environmentally significant
genotoxin, ionizing radiation. Subsequently mutation frequencies will be
measured in discrete populations of spermatogenic cells to directly
determine: 1) if there is a differential mutability among spermatogenic
cells and 2) if mutation frequencies correlate with DNA repair activities
measured in the first phase. This study will advance an understanding of
the fundamental mechanisms involved in mutagenesis in germ cells.
描述:生殖系突变可以对人类健康产生重大影响
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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Christi A Walter其他文献
Christi A Walter的其他文献
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{{ truncateString('Christi A Walter', 18)}}的其他基金
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10436348 - 财政年份:2020
- 资助金额:
$ 2.59万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10646448 - 财政年份:2020
- 资助金额:
$ 2.59万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10264033 - 财政年份:2020
- 资助金额:
$ 2.59万 - 项目类别:
The Paternal Age Effect - Enhanced Germ Cell Mutagenesis Modulated by the TRP53/APE1/MDM2 Tumor Suppressor Axis
父亲年龄效应 - TRP53/APE1/MDM2 肿瘤抑制轴调节的增强生殖细胞诱变
- 批准号:
10091650 - 财政年份:2020
- 资助金额:
$ 2.59万 - 项目类别:
Tumor Suppressors Mediate a Reduction in Male Gamete Quality with Aging
肿瘤抑制剂介导雄性配子质量随着衰老而降低
- 批准号:
9564362 - 财政年份:2017
- 资助金额:
$ 2.59万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8195926 - 财政年份:2010
- 资助金额:
$ 2.59万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
7930438 - 财政年份:2010
- 资助金额:
$ 2.59万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8259063 - 财政年份:2010
- 资助金额:
$ 2.59万 - 项目类别:
Mitochondrial DNA Damage: Cellular Responses, Aging and Disease
线粒体 DNA 损伤:细胞反应、衰老和疾病
- 批准号:
8397515 - 财政年份:2010
- 资助金额:
$ 2.59万 - 项目类别:
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