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Deep Trench Single-cell Genomics

Deep Trench Single-cell Genomics
深沟单细胞基因组学
批准号:
0827051
负责人:
Douglas Bartlett
金额:
$65.8万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-01 至 2014-08-31

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中文摘要
翻译
深海环境微生物多样性高,微生物的进化和分布受到高压、低温、低碳、无光等极端因素的影响。来自加州大学圣地亚哥分校和波多黎各-马亚圭斯大学的科学家们将通过集中在大西洋最深处的波多黎各海沟这一地点,探索特别极端的深海环境(深海海沟)中微生物的生物多样性。深沟原核生物(细菌和古细菌)有望拥有新的酶和细胞特性,使它们能够在这些极端条件下生存和生长。该项目的一个主要目标是研究这些微生物的基因组,以了解它们进化出的在这种恶劣环境中生存的能力。另一个目标是评估这些深沟微生物基因组中新蛋白质家族的范围和多样性。从海沟中采集水样,并在非常高的压力(80mpa或11000 psi)下保存,将使用单细胞基因组技术进行检测。将制定仔细的分选程序,以避免污染,嵌合体(两个或多个不同基因组的杂交)和其他样品处理的人工制品。这些研究人员将通过显微操作从水样中收集200个单个细胞,并在纳升体积的微流控室中扩增它们的基因组DNA。他们将对每个样本进行16S rDNA(通用标记基因)测序,作为独立的遗传标识符。然后,他们将选择具有新的系统发育特征的基因组DNA候选人进行进一步的全基因组测序。封闭和组装的基因组序列将被注释以指定基因功能。这些研究人员将这些基因组序列与来自各种海洋宏基因组数据集的序列进行比较,并将这些基因组中新蛋白质家族的范围和多样性与全球海洋调查数据集中确定的大量蛋白质家族进行比较。这些研究人员希望通过这种方式发现深海微生物的预期和意想不到的特性。他们的外联活动将包括与深海微生物界的多个讲习班,以及举办一个关于高压生物科学和生物技术的国际会议。由于深海海沟的微生物样本很难获得,因此基因组序列也将成为一种罕见的群落资源。
英文摘要
Microbial diversity in deep-sea environments is high, where microbial evolution and distribution have been influenced by extreme factors such as high pressure, low temperature, low carbon and no light. Scientists from the University of California San Diego and University of Puerto Rico-Mayaguez will explore the biodiversity of microorganisms of particularly extreme deep-sea environments - deep-sea trenches - by focusing on one site, the Puerto Rico Trench, the deepest part of the Atlantic Ocean. Deep trench prokaryotes (bacteria and archaea) are expected to possess novel enzymes and cell properties which allow them to survive and grow under these extreme conditions. One major goal of this project is to study the genomes of these microorganisms to understand what capabilities they have evolved to live in this harsh environment. Another goal is to evaluate the extent and diversity of novel protein families in the genomes of these deep trench microbes. Water samples collected from the trench and maintained under very high pressure (80 MPa or 11,000 psi), will be examined using single-cell genomic technology. A careful sorting procedure will be developed to avoid contamination, chimeras (hybridization of two or more different genomes) and other artifacts of sample handling. These researchers will collect two hundred individual cells from the water sample by micromanipulation and amplify their genomic DNA in nanoliter volume microfluidic chambers. They will perform 16S rDNA (universal marker gene) sequencing on each sample as an independent genetic identifier. They will then select genomic DNA candidates with novel phylogenetic characteristics for further full genome sequencing. The closed and assembled genome sequences will be annotated to assign gene function. These researchers will compare these genome sequences with sequences from various marine metagenomic datasets and will also compare the extent and diversity of novel protein families in these genomes to the large number of protein families identified in the Global Ocean Survey dataset. These researchers expect to discover anticipated as well as unexpected properties of deep sea microorganisms in this manner. Their outreach activities will include multiple workshops with the deep sea microbiology community and the development of an international conference on High Pressure Bioscience and Biotechnology. The genome sequences will also become a rare community resource since microbial samples from deep sea trenches are very difficult to obtain.
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会议论文
Collaborative Research: Influence of pressure on microbial communities in subseafloor sediment at hadal, abyssal, bathyal, and shelf water depths
Collaborative Research: Transcriptional Adaptation and Response to Pressure
Patterns of Microbial Community Structure Within and Between Hadal Environments
US-EC Workshop on Marine Genomics: Next Generation Scientists for Next Generation Sequencing, October 10-12, 2010, Washington, DC
国内基金
海外基金
绿光激光器InGaN量子阱有源区trench缺陷微观结构与形成机理研究