Bechtel Stephanie, Rosenfelder Heiko, Duda Anny, Schmidt Christian Peter, Ernst Ute, Wellenreuther Ruth, Mehrle Alexander, Schuster Claudia, Bahr Andre, Blöcker Helmut, Heubner Dagmar, Hoerlein Andreas, Michel Guenter, Wedler Holger, Köhrer Karl, Ottenwälder Birgit, Poustka Annemarie, Wiemann Stefan, Schupp Ingo
Department of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
BMC Genomics. 2007 Oct 31;8:399. doi: 10.1186/1471-2164-8-399.
With the completion of the human genome sequence the functional analysis and characterization of the encoded proteins has become the next urging challenge in the post-genome era. The lack of comprehensive ORFeome resources has thus far hampered systematic applications by protein gain-of-function analysis. Gene and ORF coverage with full-length ORF clones thus needs to be extended. In combination with a unique and versatile cloning system, these will provide the tools for genome-wide systematic functional analyses, to achieve a deeper insight into complex biological processes.
Here we describe the generation of a full-ORF clone resource of human genes applying the Gateway cloning technology (Invitrogen). A pipeline for efficient cloning and sequencing was developed and a sample tracking database was implemented to streamline the clone production process targeting more than 2,200 different ORFs. In addition, a robust cloning strategy was established, permitting the simultaneous generation of two clone variants that contain a particular ORF with as well as without a stop codon by the implementation of only one additional working step into the cloning procedure. Up to 92 % of the targeted ORFs were successfully amplified by PCR and more than 93 % of the amplicons successfully cloned.
The German cDNA Consortium ORFeome resource currently consists of more than 3,800 sequence-verified entry clones representing ORFs, cloned with and without stop codon, for about 1,700 different gene loci. 177 splice variants were cloned representing 121 of these genes. The entry clones have been used to generate over 5,000 different expression constructs, providing the basis for functional profiling applications. As a member of the recently formed international ORFeome collaboration we substantially contribute to generating and providing a whole genome human ORFeome collection in a unique cloning system that is made freely available in the community.
随着人类基因组序列的完成,对编码蛋白质的功能分析和特性鉴定已成为后基因组时代的下一个紧迫挑战。迄今为止,缺乏全面的开放阅读框组(ORFeome)资源阻碍了蛋白质功能获得性分析的系统应用。因此,需要扩展全长开放阅读框(ORF)克隆的基因和ORF覆盖范围。结合独特且通用的克隆系统,这些将为全基因组系统功能分析提供工具,以更深入地了解复杂的生物学过程。
在此,我们描述了应用Gateway克隆技术(Invitrogen)生成人类基因全ORF克隆资源的过程。开发了一个高效克隆和测序的流程,并实施了一个样本跟踪数据库,以简化针对2200多个不同ORF的克隆生产过程。此外,建立了一种稳健的克隆策略,通过在克隆过程中仅增加一个额外的操作步骤,允许同时生成包含特定ORF且带有和不带有终止密码子的两种克隆变体。高达92%的目标ORF通过聚合酶链反应(PCR)成功扩增,超过93%的扩增子成功克隆。
德国cDNA联盟ORFeome资源目前由超过3800个经过序列验证的入门克隆组成,这些克隆代表了约1700个不同基因位点的ORF,有或没有终止密码子。克隆了177个剪接变体,代表其中121个基因。入门克隆已用于生成超过5000个不同的表达构建体,为功能分析应用提供了基础。作为最近成立的国际ORFeome合作组织的成员,我们在一个独特的克隆系统中极大地推动了全基因组人类ORFeome集合的生成和提供,并在科学界免费提供。