POPULATION GENETICS OF TRANSPOSABLE ELEMENTS
转座元件的群体遗传学
基本信息
- 批准号:3283686
- 负责人:
- 金额:$ 20.89万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1984
- 资助国家:美国
- 起止时间:1984-07-01 至 1989-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The population genetics of copia-like transposable elements in Drosophila
will be investigated, with special reference to their ability to be
transferred horizontally among species and their extent of sequence
divergence among related species. Three specific aims will be pursued:
1. Heterologous transformation will be developed in order to transfer
transposable elements among species. Initially, the P-element-mediated
rosy transformation system will be used to transform D. simulans with DNA
from D. melanogaster. Successful transformation will establish the ability
of P to transpose in genomes other than that of D. melanogaster.
Subsequent experiments will determine how widely among Drosophila species
this element can be disseminated and still remain transposable. In
addition, P-bearing cotransformants will be studied in order to determine
whether hybrid dysgenesis, a complex syndrome of germ-line abnormalities
associated with P element in D. melanogaster, also occurs in other species
into which P has been introduced. These experiments will provide
information about host-element interactions in transposition, and they will
permit evaluation of the postulated role of P-like elements in speciation.
2. A highly unstable white allele in D. mauritiana will be studied
genetically and at the molecular level to characterize an inserted DNA
element. This mutant is of interest because D. mauritiana and D. simulans
have many fewer copia-like elements than their sibling species D.
melanogaster. Transposable elements that are retained in D. mauritiana and
D. simulans may therefore have certain unusual properties. These studies
may explain why transposable elements of a given family are not distributed
among species as would be expected from their phylogenetic affiliation. In
the long run the unstable white allele will be transformed into D.
melanogaster in order to study its mutational characteristics in an alien
genome.
3. The transposable element copia will be studied among related species of
Drosophila in order to determine the extent of restriction-map variation
within and among species. Several copias differing in restriction map
occur in D. melanogaster, and copia in D. mauritiana differs from that in
D. melanogaster. Our studies will focus on strains collected relatively
recently. These studies will reveal whether concerted evolution occurs in
dispersed repeated multigene families, which will be important in
evaluating the relative role of the evolutionary forces that impinge upon
such elements.
果蝇Copia样转座因子的群体遗传学研究
将被调查,特别是他们的能力,
物种间的水平转移及其序列范围
相关物种之间的差异。 将追求三个具体目标:
1. 将开发异源转化,以转移
物种间的转座因子 最初,P元件介导的
玫瑰变换系统将D.模拟DNA
来自D.黑腹菌 成功的转型将建立能力
在D基因组以外的基因组中转座。黑腹菌
接下来的实验将确定果蝇物种中
该元件可以被散布并且仍然保持可转座。 在
此外,将研究含P共转化体以确定
无论是杂种发育不全,一种复杂的生殖系异常综合征,
与D中的P元素有关。也发生在其他物种中
其中P被引入。 这些实验将提供
关于转座中宿主元件相互作用的信息,它们将
允许的P-样元素在物种形成的假定作用的评价。
2. D.一个高度不稳定的白色等位基因。将研究毛里求斯
在基因和分子水平上表征插入的DNA
元素 该突变体是令人感兴趣的,因为D. mauritiana和D. simulans
比它们的兄弟物种D具有更少的copia样元素。
黑腹菌 转座因子保留在D.毛里求斯和
D.因此,仿真物可能具有某些不寻常的性质。 这些研究
可以解释为什么一个特定家族的转座因子不分布在
在物种之间,正如从它们的系统发育关系所预期的那样。 在
从长远来看,不稳定的白色等位基因将转化为D。
为了研究它在一个外来物种中的突变特征,
基因组
3. 转座因子copia将在相关物种中进行研究
果蝇,以确定限制图谱变异的程度
在不同物种之间。 限制性酶切图谱的几个不同拷贝
发生在D。melanogaster和copia在D.毛里求斯与
D.黑腹菌 我们的研究将集中在相对收集的菌株
最近 这些研究将揭示协同进化是否发生在
分散重复的多基因家族,这将是重要的,
评估进化力量的相对作用,
这样的元素。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Daniel L HARTL其他文献
Daniel L HARTL的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Daniel L HARTL', 18)}}的其他基金
Evolutionary medicine in the development of antimalaria drugs
抗疟疾药物开发中的进化医学
- 批准号:
8691243 - 财政年份:2014
- 资助金额:
$ 20.89万 - 项目类别:
Evolutionary medicine in the development of antimalaria drugs
抗疟疾药物开发中的进化医学
- 批准号:
8820233 - 财政年份:2014
- 资助金额:
$ 20.89万 - 项目类别:
Evolutionary medicine in the development of antimalaria drugs
抗疟疾药物开发中的进化医学
- 批准号:
9198129 - 财政年份:2014
- 资助金额:
$ 20.89万 - 项目类别:
Genetic Variation and Evolution of Artemisinin Resistance
青蒿素耐药性的遗传变异和进化
- 批准号:
9026563 - 财政年份:2013
- 资助金额:
$ 20.89万 - 项目类别:
Genetic Variation and Evolution of Artemisinin Resistance
青蒿素耐药性的遗传变异和进化
- 批准号:
8822805 - 财政年份:2013
- 资助金额:
$ 20.89万 - 项目类别:
Genetic Variation and Evolution of Artemisinin Resistance
青蒿素耐药性的遗传变异和进化
- 批准号:
8439482 - 财政年份:2013
- 资助金额:
$ 20.89万 - 项目类别:
Genetic Variation and Evolution of Artemisinin Resistance
青蒿素耐药性的遗传变异和进化
- 批准号:
8649014 - 财政年份:2013
- 资助金额:
$ 20.89万 - 项目类别:
Novel Genetic Mechanism of Artemisinin Resistance for Malaria
青蒿素抗疟疾的新遗传机制
- 批准号:
10201429 - 财政年份:2013
- 资助金额:
$ 20.89万 - 项目类别:
Novel genomic effects of Y-linked polymorphisms
Y连锁多态性的新基因组效应
- 批准号:
8034816 - 财政年份:2009
- 资助金额:
$ 20.89万 - 项目类别:
Novel genomic effects of Y-linked polymorphisms
Y连锁多态性的新基因组效应
- 批准号:
7758771 - 财政年份:2009
- 资助金额:
$ 20.89万 - 项目类别:
相似海外基金
Linkage of HIV amino acid variants to protective host alleles at CHD1L and HLA class I loci in an African population
非洲人群中 HIV 氨基酸变异与 CHD1L 和 HLA I 类基因座的保护性宿主等位基因的关联
- 批准号:
502556 - 财政年份:2024
- 资助金额:
$ 20.89万 - 项目类别:
Olfactory Epithelium Responses to Human APOE Alleles
嗅觉上皮对人类 APOE 等位基因的反应
- 批准号:
10659303 - 财政年份:2023
- 资助金额:
$ 20.89万 - 项目类别:
Deeply analyzing MHC class I-restricted peptide presentation mechanistics across alleles, pathways, and disease coupled with TCR discovery/characterization
深入分析跨等位基因、通路和疾病的 MHC I 类限制性肽呈递机制以及 TCR 发现/表征
- 批准号:
10674405 - 财政年份:2023
- 资助金额:
$ 20.89万 - 项目类别:
An off-the-shelf tumor cell vaccine with HLA-matching alleles for the personalized treatment of advanced solid tumors
具有 HLA 匹配等位基因的现成肿瘤细胞疫苗,用于晚期实体瘤的个性化治疗
- 批准号:
10758772 - 财政年份:2023
- 资助金额:
$ 20.89万 - 项目类别:
Identifying genetic variants that modify the effect size of ApoE alleles on late-onset Alzheimer's disease risk
识别改变 ApoE 等位基因对迟发性阿尔茨海默病风险影响大小的遗传变异
- 批准号:
10676499 - 财政年份:2023
- 资助金额:
$ 20.89万 - 项目类别:
New statistical approaches to mapping the functional impact of HLA alleles in multimodal complex disease datasets
绘制多模式复杂疾病数据集中 HLA 等位基因功能影响的新统计方法
- 批准号:
2748611 - 财政年份:2022
- 资助金额:
$ 20.89万 - 项目类别:
Studentship
Genome and epigenome editing of induced pluripotent stem cells for investigating osteoarthritis risk alleles
诱导多能干细胞的基因组和表观基因组编辑用于研究骨关节炎风险等位基因
- 批准号:
10532032 - 财政年份:2022
- 资助金额:
$ 20.89万 - 项目类别:
Recessive lethal alleles linked to seed abortion and their effect on fruit development in blueberries
与种子败育相关的隐性致死等位基因及其对蓝莓果实发育的影响
- 批准号:
22K05630 - 财政年份:2022
- 资助金额:
$ 20.89万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Investigating the Effect of APOE Alleles on Neuro-Immunity of Human Brain Borders in Normal Aging and Alzheimer's Disease Using Single-Cell Multi-Omics and In Vitro Organoids
使用单细胞多组学和体外类器官研究 APOE 等位基因对正常衰老和阿尔茨海默病中人脑边界神经免疫的影响
- 批准号:
10525070 - 财政年份:2022
- 资助金额:
$ 20.89万 - 项目类别:
Leveraging the Evolutionary History to Improve Identification of Trait-Associated Alleles and Risk Stratification Models in Native Hawaiians
利用进化历史来改进夏威夷原住民性状相关等位基因的识别和风险分层模型
- 批准号:
10689017 - 财政年份:2022
- 资助金额:
$ 20.89万 - 项目类别: