课题基金 / 基金详情

Rates of DNA Sequence Change on Avian Chromosomes: A Test of the Replicative Division Hypothesis

Rates of DNA Sequence Change on Avian Chromosomes: A Test of the Replicative Division Hypothesis
禽类染色体 DNA 序列变化率:复制分裂假说的检验
批准号:
9629462
负责人:
Thomas Quinn
金额:
$21.0万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-09-01 至 2000-08-31

项目摘要

项目成果

Thomas Quinn的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
9629462 QUINN Evidence that DNA or protein sequences change at a steady rate through time was presented in the early 1960s, and now comprises the rationale for using amounts of sequence divergence to estimate how long ago species pairs diverged from each other. This has become known as the "molecular clock". Just how steady that rate is has been a matter of considerable debate. In particular, there has been recent interest in what the "motor" is that determines the rate at which the clock "ticks". One hypothesis is that DNA mutation occurs primarily during replication and that the rate is determined by number of rounds of replication encountered by germ line cell lineages per unit of time. This may explain why, for instance, mice evolve more quickly than humans at the sequence level. If this hypothesis is correct, then DNA within chromosomes that are passed on primarily through male or primarily through female vertebrate lineages should evolve at different rates because females use fewer numbers of rounds of replication in the production of gametes than do males. While this trend has been observed in mammals, other interpretations of the meaning of this result are possible. In this study, Thomas W. Quinn will compare rates of DNA sequence change within the W, Z and autosomal chromosomes in birds. Molecular techniques will be used to identify and sequence comparable DNA sequences found on the W and at least one other chromosome. The rate of change in these sequences will be measured and compared with the predicted result, that sequences on the W chromosome will show fewer changes than comparable sequences on other chromosomes. This is an important addition to mammalian studies because there is a female-specific chromosome in birds rather than a male-specific chromosome as in mammals. The bird study system presents an opportunity to test the hypothesis of the dependence of DNA mutation rate on frequency of DNA replication, in a case where rate differences between various chromosomes are predicted to be different in direction and magnitude from those found on mammalian chromosomes.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Collaborative Research: Galactic Winds and the Multiphase Structure of the Circum-Galactic Medium
  • 批准号:
    2205724
  • 项目类别:
    Standard Grant
  • 资助金额:
    $43.95万
  • 财政年份:
    2022
  • 负责人:
    Thomas Quinn
  • 依托单位:
In Situ Formation of Short Period Terrestrial Planets
  • 批准号:
    2006752
  • 项目类别:
    Standard Grant
  • 资助金额:
    $45.13万
  • 财政年份:
    2020
  • 负责人:
    Thomas Quinn
  • 依托单位:
OAC Core: Small: Collaborative Research: Scalable distributed algorithms for tree structured astronomical data
  • 批准号:
    1906829
  • 项目类别:
    Standard Grant
  • 资助金额:
    $14.58万
  • 财政年份:
    2019
  • 负责人:
    Thomas Quinn
  • 依托单位:
SI2-SSI: Collaborative Research: Paratreet: Parallel Software for Spatial Trees in Simulation and Analysis
  • 批准号:
    1550234
  • 项目类别:
    Standard Grant
  • 资助金额:
    $14.0万
  • 财政年份:
    2016
  • 负责人:
    Thomas Quinn
  • 依托单位:
国内基金
海外基金
自供能传感阵列同步量化游离DNA与PSA实现前列腺癌的诊断和预后判断
  • 批准号:
    JCZRLH202601177
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
  • 依托单位:
二氢杨梅素通过线粒体代谢重编程抑制DNA同源重组修复逆转口腔癌细胞放疗抵抗的机制研究
  • 批准号:
    2026JJ80500
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    阳帆
  • 依托单位:
乳酸通过ESM1-Akt-MDM2-p53通路调控卵巢癌DNA损伤和抗肿瘤免疫应答的分子机制研究
  • 批准号:
    2026JJ81975
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2026
  • 负责人:
    肖娇
  • 依托单位:
淫羊藿苷通过TET2介导DNA去甲基化调控Hippo-YAP/TAZ通路逆转绝经后骨质疏松症成血管-成骨耦联失衡的机制研究