EVOLUTION AND DIVERSITY OF EUKARYOTIC GLYCOSYLATION

真核糖基化的进化和多样性

• 批准号: 7602028
• 负责人: PHILLIPS W ROBBINS
• 金额: $ 0.65万
• 依托单位: BOSTON UNIVERSITY MEDICAL CAMPUS
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-03 至 2008-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7602028
• 关键词: Bioinformatics; Computer Retrieval of Information on Scientific Projects Database; Dolichol; Entamoeba histolytica; Evolution; Funding; Giardia lamblia; Golgi Apparatus; Grant; Human; Institution; Leishmania; Link; Modeling; Modification; Oligosaccharides; Polysaccharides; Protein Glycosylation; Proteins; Proteome; Research; Research Personnel; Resources; Saccharomyces cerevisiae; Source; Trichomonas vaginalis; Trypanosoma; United States National Institutes of Health; base; genome sequencing; glycosylation; positional cloning; research study

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. While Saccharomyces cerevisiae has been a good model for human N- and O-linked glycosylation and GPI-anchor synthesis, most of the evolution and diversity in protein glycosylation exists among deeply divergent protists. Glycosylation of kinetoplastids (e.g. Trypanosoma sp. and Leishmania sp.) has been extensively studied, but glycosylation of microaerophilic protists (Trichomonas vaginalis, Giardia lamblia (GI), and Entamoeba histolytica (Eh) are not well studied. Whole genome sequences that predict the total proteins (proteome) are now available for all of these protist species. Preliminary evidence of the diversity of eukaryotic glycosylation based upon our bioinformatics/ experimental approach predict that Eh and Tv make abbreviated dolichol-linked N-glycan precursors. Preliminary experiments demonstrate that Eh and Tv do, indeed, synthesize abbreviated dolichol-linked N-glycan precursors. Therefore, the truncated precursors will likely be the starting point for any subsequent modifications. However, reverse genetics may not predict modifications that are specific to the niche of a given protest and, therefore, structural studies will be conducted to determine if the oligosaccharides are modified by additional Golgi or Golgi-like modifications or if they are simply truncated as found in, Trypanosomes.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 虽然酿酒酵母是人类N-和O-连接糖基化和GPI锚合成的良好模型，但蛋白质糖基化的大部分进化和多样性存在于差异很大的原生生物中。 动质体（例如锥虫属和利什曼原虫属）的糖基化已被广泛研究，但微需氧原生生物（迷走毛滴虫、兰氏贾第鞭毛虫（GI）和溶组织内阿米巴（Eh））的糖基化尚未得到充分研究。 全基因组序列，预测总蛋白质（蛋白质组），现在可用于所有这些原生生物物种。 基于我们的生物信息学/实验方法的真核生物糖基化的多样性的初步证据预测，Eh和Tv使缩写的长链连接的N-聚糖前体。 初步实验表明，Eh和Tv确实合成了缩短的长醇连接的N-聚糖前体。 因此，截短的前体将可能是任何后续修改的起点。 然而，反向遗传学可能无法预测特定于特定抗议生态位的修饰，因此，将进行结构研究以确定寡糖是否被额外的高尔基体或高尔基体样修饰修饰，或者它们是否被简单地截短，如锥虫中所发现的那样。