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Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.

作者信息

Irving N G, Brown S D

机构信息

Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, London, United Kingdom.

出版信息

Genomics. 1991 Nov;11(3):679-86. doi: 10.1016/0888-7543(91)90075-p.

Abstract

We have utilized an oligonucleotide primer from the 3' end of the mouse L1 repeat element for amplification of mouse-specific inter-repeat PCR products from Chinese hamster/mouse somatic cell hybrids. PCR of a Chinese hamster/mouse somatic cell hybrid (96AZ2), containing only mouse chromosome 16, produced a range of mouse-specific bands. Two of the mouse-specific PCR products, of 250 and 580 bp, have been confirmed as originating from mouse chromosome 16 by somatic cell hybrid analysis. Both the 250- and 580-bp PCR products have been sequenced and demonstrate the expected sequence organization. Furthermore, both the 250- and 580-bp markers have been genetically mapped in detail to mouse chromosome 16 by direct hybridization to inter-repeat PCR products of progeny DNAs from Mus domesticus/Mus spretus interspecific backcrosses.

摘要

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引用本文的文献

1
Dispersed repetitive elements in mouse genome analysis.
Mamm Genome. 1992;2(4):207-14. doi: 10.1007/BF00355430.
2
Mouse chromosome 16.
Mamm Genome. 1992;3 Spec No:S233-40. doi: 10.1007/BF00648434.

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