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使用参考文库和杂交指纹图谱的关系基因组分析。

Relational genome analysis using reference libraries and hybridisation fingerprinting.

作者信息

Hoheisel J D, Ross M T, Zehetner G, Lehrach H

机构信息

German Cancer Research Centre, Heidelberg.

出版信息

J Biotechnol. 1994 Jun 30;35(2-3):121-34. doi: 10.1016/0168-1656(94)90031-0.

Abstract

The genomes of eukaryotic organisms are studied by an integrated approach based on hybridisation techniques. For this purpose, a reference library system has been set up, with a wide range of clone libraries made accessible to probe hybridisation as high density filter grids. Many different library types made from a variety of organisms can thus be analysed in a highly parallel process; hence, the amount of work per individual clone is minimised. In addition, information produced on one analysis level instantly assists in the characterisation process on another level. Genetic, physical and transcriptional mapping information and partial sequencing data are obtained for the individual library clones and are cross-referenced toward a comprehensive molecular understanding of genome structure and organisation, of encoded functions and their regulation. The order of genomic clones is established by hybridisation fingerprinting procedures. On these physical maps, the location of transcripts is determined. Complementary, partial sequence information is produced from corresponding cDNAs by hybridising short oligonucleotides, which will lead to the identification of regions of sequence conservation and the constitution of a gene inventory. The hybridisation analysis of the cDNA clones, and the genomic clones as well, could potentially be expanded toward a determination of (nearly) the complete sequence. The accumulated data set will provide the means to direct large-scale sequencing of the DNA, or might even make the sequence analysis of large genomic regions a redundant undertaking due to the already collected information.

摘要

真核生物的基因组通过基于杂交技术的综合方法进行研究。为此,已建立了一个参考文库系统,其中有各种各样的克隆文库可作为高密度滤膜网格用于探针杂交。因此,许多来自不同生物体的不同文库类型可以在一个高度并行的过程中进行分析;从而,每个单独克隆的工作量被最小化。此外,在一个分析层面产生的信息能立即辅助另一个层面的特征化过程。针对各个文库克隆获得遗传、物理和转录图谱信息以及部分测序数据,并进行交叉参考,以全面分子理解基因组结构和组织、编码功能及其调控。基因组克隆的顺序通过杂交指纹图谱程序确定。在这些物理图谱上,确定转录本的位置。通过短寡核苷酸杂交从相应的cDNA产生互补的部分序列信息,这将导致序列保守区域的鉴定和基因清单的构建。cDNA克隆以及基因组克隆的杂交分析有可能扩展到(近乎)完整序列的测定。积累的数据集将为指导DNA的大规模测序提供手段,或者甚至可能由于已经收集到的信息而使大基因组区域的序列分析成为多余的工作。

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