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DNA指纹图谱探针pITZ1的特征。

Features of the DNA fingerprinting probe pITZ1.

作者信息

Huebscher K J, Dolf G, Frey J, Stranzinger G, Gaillard C

机构信息

Institute of Animal Breeding, University of Berne, Switzerland.

出版信息

Anim Genet. 1995 Feb;26(1):27-30. doi: 10.1111/j.1365-2052.1995.tb02615.x.

Abstract

Stringently controlled plasmids generate DNA fingerprint patterns in mammals when used at low hybridization temperatures. In order to develop a probe for use in paternity testing in cattle we screened a bovine, partial genomic plasmid library with the PCR-amplified ori region of plasmid P1. Of eight isolated clones one generated strong band patterns at high stringency in various mammalian species (data not shown). Sequence analysis revealed an imperfect, compound dinucleotide repeat region, which was PCR-amplified and cloned into the plasmid vector pUC19. Fingerprint results generated by this probe (termed pITZ1) in cattle are compared with the results generated by VNTR-probe pV47, which itself was developed by screening a human chromosome 16 library with tandem repeats of bacteriophage M13. Probe pITZ1 is useful in conjunction with other VNTR-probes for DNA fingerprinting in cattle and donkey populations. The dinucleotide repeat region responsible for the band patterns generated with pITZ1 is close to an Alu-like sequence, which may be involved in eukaryotic replication mechanisms.

摘要

当在低杂交温度下使用时,严格控制的质粒会在哺乳动物中产生DNA指纹图谱。为了开发一种用于牛亲子鉴定的探针,我们用质粒P1的PCR扩增ori区域筛选了一个牛的部分基因组质粒文库。在八个分离的克隆中,有一个在各种哺乳动物物种中在高严谨度下产生了强条带模式(数据未显示)。序列分析揭示了一个不完美的复合二核苷酸重复区域,该区域经PCR扩增后克隆到质粒载体pUC19中。将该探针(称为pITZ1)在牛中产生的指纹结果与VNTR探针pV47产生的结果进行比较,pV47本身是通过用噬菌体M13的串联重复序列筛选人类16号染色体文库而开发的。探针pITZ1与其他VNTR探针结合可用于牛和驴群体的DNA指纹分析。负责pITZ1产生条带模式二核苷酸重复区域靠近一个类似Alu的序列,这可能参与真核生物复制机制。

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