992 resultados para cDNA Library


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Planning the management of data at proposal time and throughout its lifecycle is becoming increasingly important to funding agencies and is essential to ensure its current usability and long term preservation and access. This presentation will describe the work being done at the Woods Hole Oceanographic Institution (WHOI) to assist PIs with the preparation of data management plans and the role the Library has in this process. Data management does not mean simply storing information. The emphasis is now on sharing data and making research accessible. Topics to be covered include educating staff about the NSF data policy implementation, a data management survey, resources for proposal preparation, collaborating with other librarians, and next steps.

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I have been asked by administration, how much of our collection could go into storage. They optimistically hoping for a room or two for faculty/staff offices, as some buildings need renovation or need to be closed due to safety issues. Clearly, much of the population believes that all/most library materials are available on-line – free. I will present the results of our survey’s of material held and available on-line and space “freed” thanks to archiving. How little space is freed.

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The first concept of a new library was introduced in 2001 by a faculty member at the University of Texas Marine Science Institute. The suggestion for the construction of a new library was based on two specific reasons: existing library is located in one of the most vulnerable buildings to hurricane damage and the library has outgrown its current space. This presentation provides a general overview of the current status and changing needs of the Marine Science Library and how the idea of a new library finally became a reality

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The purpose of this article is to update and build on the approximate 10,000 item collection of the Harbor Branch Oceanographic Institute Library. This article will present a history of Harbor Branch and its library, and a literature review, outlining the collection development methods of other marine science libraries and academic libraries. The article will relate brief histories of three marine science libraries. A comparative table is constructed to compare Harbor Branch Library with three marine science libraries. The methodology, or how the table was created, is explained. The comparative table will be shown and analyzed, and the results of the table discussed. Finally, some recommendations for improvement of the Harbor Branch Library will be presented.

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日益加剧的重金属污染已经危害到了全球的生态环境以及人类健康。在分子水平上阐明植物中的重金属抗性机制并应用于环境修复和绿色农业是植物科学和环境科学以及农业科学的交叉点和新的生长点。为了了解植物重金属抗性的分子机制,我们的研究主要是从重金属抗性植物材料大蒜(Allium sativumL.)和绊根草(Cynodon dactylon)中分离重金属抗性相关基因,并研究它们在重金属抗性机制中的功能。 在高等植物中有迹象表明,一种富含半胱氨酸的低分子量蛋白.类金属硫蛋白 (Metallothioneins Like,MTs Like)和一类具有Y-(Glu-Cys) n-Gly特殊结构的多肽一植物络合素(Phytochelatins,PCs)在重金属抗性机制中占有重要地位。然而人们对于同一种植物中这两种重金属结合肽作用的相互关系还缺乏了解,同时对于MT Like基因以及PCs合酶基因在同一种植物中的表达模式如金属离子专一性、时空表达特点等,还投有文献报道,因此本文将首先以这两个基因为切入点进行研究。 本研究采用RACE的方法,从大蒜中分离得到了类金属硫蛋白(MT-Like)的cDNA序列(GenBank Accession No.AY050510),PCR和SoutheLrn Blot分析表明,大蒜基因组中不仅存在类金属硫蛋白基因,而且可能以基因家族的形式存在。对获得的MT Like cDNA进行的序列分析及同源性分析表明,大蒜MT Like cDNA含有一个完整的开放阅读框架,编码73个氨基酸,其中12个为半胱氨酸,占氨基酸总数的1 6.4%,并与其他植物如水稻、小麦、紫羊茅草中的类金属硫蛋白基因同源性较高,其中最高达89%。对该基因编码的氨基酸序列和结构分析表明在N-端、c-端结构域中分别含有3个典型的金属硫蛋白的结构模式Cys-Xaa-Cys,属于典型的Type-1类金属硫蛋白。这些Cys-Xaa-Cys特征结构表明大蒜MT Like基因编码的蛋白可以结合二价金属离子。重金属胁迫下大蒜根中MT Like基因在转录水平的表达检测表明,MT Like基因的表达受重金属离子Cu2+、Cd2+的诱导,暗示MT Like基因在大蒜对重金属的抗性中有重要作用。此外,用能谱电镜技术研究大蒜中重金属的积累与分布,以及用组织原位杂交技术分析MT Like基因的表达定位与重金属的积累、转运的关系已在进行之中。 植物络合素也是富含巯基的多肽化合物,在重金属抗性中起重要作用。由植物络合素结构中存在的Y一酰胺键或β-Ala可知PCs不是基因表达的直接产物,而是以GSH为前体的酶促反应产物。目前已知y一谷氨酰半胱氨酸二肽转肽酶(简称为PCs合酶,phytochelatin synthase,PCS)是PCs合成途径的关键酶,编码这一关键酶的基因目前已在小麦、拟南芥菜和裂殖酵母中克隆。由于这一基因在不同物种中的保守性较低,其克隆较困难。本研究通过设计植物络合素台酶基因简并引物,从大蒜中扩增得到了345bp的cDNA序列。序列分析和推测的氨基酸序列同源性比较表明,此序列的翻译产物与已知的植物络合素合酶同源性最高,此cDNA序列应为大蒜植物络合素合酶基因的部分cDNA序列(GenBank Accession No.AF384110)。目前大蒜植物络台素合酶基因的全长序列的扩增,以及这两种与重金属抗性有关的基因(MT Like,PCS)的表达模式仍在研究中。 本文还尝试了利用酵母重金属敏感突变株M379/8功能互补的方法从重金属抗性植物绊根革中分离新的重金属抗性相关基因。构建了用于转化的酵母质粒表达文库,探索了酵母转化体系建立的条件。曾尝试多种转化方法,并对其中的条件进行了优化改进。下一步的工作将集中在合适的酵母突变体的筛选或穿梭表达载体的选择标记基因替换上