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Method of isolating exonic gene segments of eukaryotic genes, exon trapping vectors for use therein

机译:分离真核基因的外显子基因片段的方法,用于其中的外显子捕获载体

摘要

Method of isolating exonic gene segments of a eukaryotic gene by preparing a loaded exon trapping vector, bringing the loaded exon trapping vector in an environment in which transcription of DNA to RNA and RNA processing can occur, isolating processed RNA which includes exonic gene segments of the eukaryotic gene and, optionally, preparing a DNA copy of the isolated processed RNA. The loaded exon trapping vector comprises a large-insert DNA vector containing a segmented donor gene construct and, inserted in or close to said segmented donor gene construct, a target DNA fragment of at least 10 kb of eukaryotic genomic DNA. Use of vectors containing large genomic inserts allows to isolate exonic gene segments present in the correct transcriptional orientation as a complete set, without need for reordering individually isolated exons and verifying their continuity from isolated cDNAs. The number of false positives is much reduced, negatives (empty products) can easily be removed, and the system allows isolation of all types of exonic gene fragments, i.e. 5'-first internal and 3'-terminal exons.
机译:通过制备负载的外显子捕获载体,将负载的外显子捕获载体置于可能发生DNA转录成RNA和RNA加工的环境中,分离真核基因的外显子基因片段的方法,分离包括RNA的外显子基因片段的经加工的RNA。真核基因,并任选制备分离的加工RNA的DNA副本。加载的外显子捕获载体包括大插入DNA载体,其包含分段的供体基因构建体,以及插入或靠近所述分段的供体基因构建体的是至少10kb的真核基因组DNA的靶DNA片段。使用包含大基因组插入片段的载体可将以正确的转录方向完整存在的外显子基因片段作为一个完整的序列进行分离,而无需重新排列各个分离的外显子并从分离的cDNA验证其连续性。假阳性的数量大大减少,阴性(空产物)可以很容易地去除,并且该系统允许分离所有类型的外显子基因片段,即5'-第一内部外显子和3'-末端外显子。

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