课题基金 / 基金详情

Sir2 in stress resistance, aging, and DNA repair

Sir2 in stress resistance, aging, and DNA repair
Sir2 在抗压、衰老和 DNA 修复方面的作用
批准号:
7765992
负责人:
David Benner Lombard
金额:
$8.75万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-06-01 至 2009-05-31

项目摘要

项目成果

David Benner Lombard的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):随着美国老年人比例的上升,与年龄相关的疾病负担也在增加。衰老是真核生物的普遍特征,然而衰老背后的分子机制仍然很大程度上不清楚。对衰老的详细分子理解可能会延缓或预防与衰老相关的退化,甚至可能延长人类的寿命。Sir2家族成员的过表达已被证明可以延长酵母和秀丽隐杆线虫的寿命,而哺乳动物Sir2家族成员SIRT1的过表达可以增加哺乳动物细胞的氧化应激抗性。这种蛋白还能使p53去乙酰化,降低p53的活性。
英文摘要
DESCRIPTION (provided by applicant): As the proportion of elderly individuals in the United States rises, the burden of age-associated disease grows. Aging is a universal feature of eukaryotic organisms, yet the molecular mechanisms underlying aging remain largely obscure. A detailed molecular understanding of aging might allow the delay or prevention of aging-associated deterioration and perhaps the extension of human lifespan. Overexpression of Sir2 family members has been shown to extend lifespan in both yeast and C. elegans, and overexpression of a mammalian Sir2 family member, SIRT1, increases oxidative stress resistance in mammalian cells. This protein also can deacetylate p53, reducing p53 activity. The overall goal of this proposal is to define the role of Sir2 family members in stress resistance, modulation of p53 activity, and aging. This analysis will be performed in mice, and entails three specific aims. (1) To define which of the murine Sir2 family members are involved in oxidative stress resistance, and to determine whether overexpression of Sir2 proteins in mice can extend murine lifespan. (2) To evaluate the genetic interaction between SIRT1 and p53. (3) To define the role of Sir2 family members in the maintenance of chromosomal stability. This application is for a Mentored Clinical Scientist Development Award (K08). The applicant is an M.D. /Ph.D. with a longstanding interest in the basic biology of aging, and residency training in Anatomic Pathology. The proposed research will take place in the laboratory of Dr. Frederick AIt at the Center for Blood Research at Harvard Medical School. The applicant previously trained in a laboratory specializing in yeast. The candidate's long-term goal is to direct an academic research group investigating the molecular mechanisms of aging and interventions to delay the onset of senescence. This training grant would serve as a critical bridge to this independent position, by allowing the candidate to study in one of the foremost mammalian labs in the country.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI: 10.18632/aging.100014
发表时间: 2009-01-20
期刊: Aging
影响因子: --
作者: [Lombard DB]
通讯作者: Lombard DB
DOI: 10.1111/j.1474-9726.2009.00503.x
发表时间: 2009-09
期刊: Aging cell
影响因子: 7.8
作者: [Schwer B, Eckersdorff M, Li Y, Silva JC, Fermin D, Kurtev MV, Giallourakis C, Comb MJ, Alt FW, Lombard DB]
通讯作者: Lombard DB
SIRT5 inhibitors and degraders as novel treatments for Ewing sarcoma
SIRT5 inhibitors and degraders as novel treatments for Ewing sarcoma
Targeting the longevity regulator PAPP-A with small molecule inhibitors
Targeting the longevity regulator PAPP-A with small molecule inhibitors
海外基金