Analysis of retina rod photoreceptor GARP and cGMP-gated cation channel

视网膜视杆光感受器 GARP 和 cGMP 门控阳离子通道的分析

基本信息

  • 批准号:
    7372754
  • 负责人:
  • 金额:
    $ 36.25万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2008
  • 资助国家:
    美国
  • 起止时间:
    2008-01-01 至 2011-12-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The long term objectives of the research program are to understand protein structure/function relationships in retinal photoreceptors, and to translate this understanding to the treatment of patients with retinitis pigmentosa and related disorders. In humans, CNGB1 gene defects cause hereditary retinal degeneration. We have therefore focused on the murine Cngbl locus that expresses, exclusively in the rod outer segment (ROS), two relatively abundant proteins: plasma membrane localized 2-subunit of the cGMP-gated cation channel and cytoplasmic glutamic acid-proline rich polypeptide (GARP-2). The rod cGMP-gated cation channel plays a critical role in vision by regulating the flow of calcium and sodium ions into the rod cell. In addition, both the 2-subunit and GARP-2 interact with peripherin-2/rds, a disk membrane protein, and thus may play essential structural roles. To determine the contribution of the proteins in ROS, we generated a homozygous Cngbl photoreceptor null (5' KO), and are analyzing the mice using light and EM level analysis, ERG and single cell recordings, and Western analysis. Homozygous 5' KO mice show a significant reduction (>30 fold) in light sensitivity and attenuated b-wave response, but are functional prior to the onset of retinal degeneration. Surprisingly, in the 59 KO not only is the 2-subunit absent but the channel 1-subunit is also greatly reduced in abundance in ROS. We hypothesize that the GARP region has an important structural role in the photoreceptor and that GARP-2, like the 2-subunit has also an important functional role. We will directly examine the structural and functional roles of the GARP region of the beta subunit and of GARP-2 by targeted deletion of GARP-2 expression and introduction of transgenes into 59 KO and 2-subunit knockout mice (39 KO). The proposed studies will help to establish the function of the Cngbl encoded GARP region and of GARP-2 in the photoreceptor, and hence provide important insights into the mechanisms whereby CNGB1 gene defects cause hereditary retinal degeneration. The studies may also yield new targets for intervention as possible treatments for certain forms of hereditary retina degeneration.
描述(由申请人提供):该研究项目的长期目标是了解视网膜光感受器中蛋白质结构/功能的关系,并将这种理解转化为视网膜色素变性和相关疾病患者的治疗。在人类中,CNGB1基因缺陷导致遗传性视网膜变性。因此,我们将重点放在小鼠Cngbl基因座上,该基因座仅在杆状外段(ROS)表达两种相对丰富的蛋白质:质膜定位的cgmp门控阳离子通道2亚基和细胞质富含谷氨酸-脯氨酸的多肽(GARP-2)。杆状细胞cgmp门控阳离子通道通过调节钙和钠离子进入杆状细胞的流动,在视觉中起关键作用。此外,2-亚基和GARP-2都与磁盘膜蛋白peripherin-2/rds相互作用,因此可能发挥重要的结构作用。为了确定这些蛋白在ROS中的作用,我们生成了一个纯合子Cngbl光受体零(5’KO),并使用光和EM水平分析、ERG和单细胞记录以及Western分析对小鼠进行分析。纯合子5' KO小鼠的光敏性和b波反应显著降低(约30倍),但在视网膜变性发生之前功能正常。令人惊讶的是,在59 KO中,不仅2亚基缺失,而且通道1亚基在ROS中的丰度也大大降低。我们假设GARP区域在光感受器中具有重要的结构作用,并且GARP-2与2亚基一样也具有重要的功能作用。我们将通过靶向删除GARP-2表达并将转基因引入59 KO和2亚基敲除小鼠(39 KO),直接研究β亚基和GARP-2的GARP区域的结构和功能作用。这些研究将有助于确定CNGB1编码的GARP区域和GARP-2在光感受器中的功能,从而为CNGB1基因缺陷导致遗传性视网膜变性的机制提供重要的见解。这些研究也可能为某些形式的遗传性视网膜变性的可能治疗提供新的干预目标。

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 }}

STEVEN J PITTLER其他文献

STEVEN J PITTLER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('STEVEN J PITTLER', 18)}}的其他基金

Noninvasive Visualization and Analysis of Organ Systems using OCT and Digital Fun
使用 OCT 和 Digital Fun 进行器官系统的无创可视化和分析
  • 批准号:
    7793095
  • 财政年份:
    2009
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated channel
视网膜视杆光感受器 GARP 和 cGMP 门控通道的分析
  • 批准号:
    8579459
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated channel
视网膜视杆光感受器 GARP 和 cGMP 门控通道的分析
  • 批准号:
    9090247
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated cation channel
视网膜视杆光感受器 GARP 和 cGMP 门控阳离子通道的分析
  • 批准号:
    8020065
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated channel
视网膜视杆光感受器 GARP 和 cGMP 门控通道的分析
  • 批准号:
    8721963
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated cation channel
视网膜视杆光感受器 GARP 和 cGMP 门控阳离子通道的分析
  • 批准号:
    7532769
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated channel
视网膜视杆光感受器 GARP 和 cGMP 门控通道的分析
  • 批准号:
    9126549
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
Analysis of retina rod photoreceptor GARP and cGMP-gated cation channel
视网膜视杆光感受器 GARP 和 cGMP 门控阳离子通道的分析
  • 批准号:
    7751248
  • 财政年份:
    2008
  • 资助金额:
    $ 36.25万
  • 项目类别:
CORE--MOLECULAR BIOLOGY
核心--分子生物学
  • 批准号:
    6990783
  • 财政年份:
    2004
  • 资助金额:
    $ 36.25万
  • 项目类别:
Vision Science Research Center
视觉科学研究中心
  • 批准号:
    8121448
  • 财政年份:
    1997
  • 资助金额:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 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:
    $ 36.25万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了