Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.

Chromosomal translocations are crucial events in the aetiology of many leukaemias, lymphomas and sarcomas, resulting in enforced oncogene expression or the creation of novel fusion genes. The study of the biological outcome of such events ideally requires recapitulation of the tissue specificity and...

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Main Authors: Collins, E, Pannell, R, Simpson, E, Forster, A, Rabbitts, T
Format: Journal article
Language:English
Published: 2000
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author Collins, E
Pannell, R
Simpson, E
Forster, A
Rabbitts, T
author_facet Collins, E
Pannell, R
Simpson, E
Forster, A
Rabbitts, T
author_sort Collins, E
collection OXFORD
description Chromosomal translocations are crucial events in the aetiology of many leukaemias, lymphomas and sarcomas, resulting in enforced oncogene expression or the creation of novel fusion genes. The study of the biological outcome of such events ideally requires recapitulation of the tissue specificity and timing of the chromosomal translocation itself. We have used the Cre-loxP system of phage P1 to induce de novo Mll-Af9 chromosomal recombination during mouse development. loxP sites were introduced into the Mll and Af9 genes on chromosomes 9 and 4, respectively, and mice carrying these alleles were crossed with mice expressing Cre recombinase. A resulting Mll-Af9 fusion gene was detected whose transcription and splicing were verified. Thus, programmed interchromosomal recombination can be achieved in mice. This approach should allow the design of mouse models of tumorigenesis with greater biological relevance than those available at present.
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spelling oxford-uuid:1703cf65-6024-4dcd-abf6-d211ba09695f2022-03-26T10:34:40ZInter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:1703cf65-6024-4dcd-abf6-d211ba09695fEnglishSymplectic Elements at Oxford2000Collins, EPannell, RSimpson, EForster, ARabbitts, TChromosomal translocations are crucial events in the aetiology of many leukaemias, lymphomas and sarcomas, resulting in enforced oncogene expression or the creation of novel fusion genes. The study of the biological outcome of such events ideally requires recapitulation of the tissue specificity and timing of the chromosomal translocation itself. We have used the Cre-loxP system of phage P1 to induce de novo Mll-Af9 chromosomal recombination during mouse development. loxP sites were introduced into the Mll and Af9 genes on chromosomes 9 and 4, respectively, and mice carrying these alleles were crossed with mice expressing Cre recombinase. A resulting Mll-Af9 fusion gene was detected whose transcription and splicing were verified. Thus, programmed interchromosomal recombination can be achieved in mice. This approach should allow the design of mouse models of tumorigenesis with greater biological relevance than those available at present.
spellingShingle Collins, E
Pannell, R
Simpson, E
Forster, A
Rabbitts, T
Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title_full Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title_fullStr Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title_full_unstemmed Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title_short Inter-chromosomal recombination of Mll and Af9 genes mediated by cre-loxP in mouse development.
title_sort inter chromosomal recombination of mll and af9 genes mediated by cre loxp in mouse development
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