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

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 1...

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Main Authors: Irving, N, Brown, S
Formato: Journal article
Idioma:English
Publicado: 1991
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author Irving, N
Brown, S
author_facet Irving, N
Brown, S
author_sort Irving, N
collection OXFORD
description 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.
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spelling oxford-uuid:c34ceac0-f673-4a08-9f5e-18bfe00774db2022-03-27T06:15:24ZMouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c34ceac0-f673-4a08-9f5e-18bfe00774dbEnglishSymplectic Elements at Oxford1991Irving, NBrown, SWe 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.
spellingShingle Irving, N
Brown, S
Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title_full Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title_fullStr Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title_full_unstemmed Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title_short Mouse chromosome-specific markers generated by PCR and their mapping through interspecific backcrosses.
title_sort mouse chromosome specific markers generated by pcr and their mapping through interspecific backcrosses
work_keys_str_mv AT irvingn mousechromosomespecificmarkersgeneratedbypcrandtheirmappingthroughinterspecificbackcrosses
AT browns mousechromosomespecificmarkersgeneratedbypcrandtheirmappingthroughinterspecificbackcrosses