Abstract |
Tumor-specific alteration of the TAL1 gene occurs in almost 25% of patients with T-cell acute lymphoblastic leukemia ( T-ALL). We now report the identification of TAL2, a distinct gene that was isolated on the basis of its sequence homology with TAL1. The TAL2 gene is located 33 kilobase pairs from the chromosome 9 breakpoint of t(7;9)(q34;q32), a recurring translocation specifically associated with T-ALL. As a consequence of t(7;9)(q34;q32), TAL2 is juxtaposed with sequences from the T-cell receptor beta-chain gene on chromosome 7. TAL2 sequences are actively transcribed in SUP-T3, a T-ALL cell line that harbors the t(7;9)(q34;q32). The TAL2 gene product includes a helix-loop-helix protein dimerization and DNA binding domain that is especially homologous to those encoded by the TAL1 and LYL1 protooncogenes. Hence, TAL2, TAL1, and LYL1 constitute a discrete subgroup of helix-loop-helix proteins, each of which can potentially contribute to the development of T-ALL.
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Authors | Y Xia, L Brown, C Y Yang, J T Tsan, M J Siciliano, R Espinosa 3rd, M M Le Beau, R J Baer |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 88
Issue 24
Pg. 11416-20
(Dec 15 1991)
ISSN: 0027-8424 [Print] United States |
PMID | 1763056
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Basic Helix-Loop-Helix Transcription Factors
- DNA, Neoplasm
- DNA-Binding Proteins
- Neoplasm Proteins
- Oligodeoxyribonucleotides
- TAL2 protein, human
- Tal2 protein, mouse
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Topics |
- Amino Acid Sequence
- Animals
- Base Sequence
- Basic Helix-Loop-Helix Transcription Factors
- Chromosomes, Human, Pair 7
- Chromosomes, Human, Pair 9
- DNA, Neoplasm
(genetics, isolation & purification)
- DNA-Binding Proteins
(genetics)
- Gene Expression Regulation, Neoplastic
- Genetic Linkage
- Humans
- Leukemia, T-Cell
(genetics)
- Leukemia-Lymphoma, Adult T-Cell
(genetics)
- Mice
- Molecular Sequence Data
- Neoplasm Proteins
(genetics)
- Oligodeoxyribonucleotides
- Open Reading Frames
- Polymerase Chain Reaction
(methods)
- Proto-Oncogenes
- Restriction Mapping
- Sequence Homology, Nucleic Acid
- Translocation, Genetic
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