Analysis of the Murine All-1 Gene Reveals Conserved Domains with Human ALL-1 and Identifies a Motif Shared with DNA Methyltransferases

A series of translocation break points found in a subset of human acute leukemias have one of the breaks on human chromosome 11q23. This region has recently been cloned and a large gene, ALL-1, with homology to the Drosophila trithorax gene has been identified. This paper describes the cloning, sequ...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 90; no. 13; pp. 6350 - 6354
Main Authors Ma, Qing, Alder, Hansjuerg, Nelson, Kelly K., Chatterjee, Devjani, Gu, Yansong, Nakamura, Tatsuya, Canaani, Eli, Croce, Carlo M., Siracusa, Linda D., Buchberg, Arthur M.
Format Journal Article
LanguageEnglish
Published Washington, DC National Academy of Sciences of the United States of America 01.07.1993
National Acad Sciences
National Academy of Sciences
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Summary:A series of translocation break points found in a subset of human acute leukemias have one of the breaks on human chromosome 11q23. This region has recently been cloned and a large gene, ALL-1, with homology to the Drosophila trithorax gene has been identified. This paper describes the cloning, sequencing, and mapping of the mouse homolog of ALL-1. We have found a motif present in All-1 that shows homology to the zinc-binding domain of DNA (cytosine-5) methyltransferases (EC 2.1.1.63). Sequence analysis of the murine All-1 gene has identified distinct regions of homology with the human ALL-1 gene; these highly conserved domains may define regions of functional significance in mammals. In addition, we have identified alternatively spliced forms of All-1 within one of the zinc-finger domains, suggesting that there may be different targets and/or functions for All-1 proteins. Finally, we report that All-1 resides in the proximal portion of mouse chromosome 9 and is a candidate for a mutation that results in skeletal transformations during embryonic development.
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ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.90.13.6350