The C-terminal SET domains of ALL-1 and TRITHORAX interact with the INI1 and SNR1 proteins, components of the SWI/SNF complex

Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4152-7. doi: 10.1073/pnas.95.8.4152.

Abstract

The ALL-1 gene was discovered by virtue of its involvement in human acute leukemia. Its Drosophila homolog trithorax (trx) is a member of the trx-Polycomb gene family, which maintains correct spatial expression of the Antennapedia and bithorax complexes during embryogenesis. The C-terminal SET domain of ALL-1 and TRITHORAX (TRX) is a 150-aa motif, highly conserved during evolution. We performed yeast two hybrid screening of Drosophila cDNA library and detected interaction between a TRX polypeptide spanning SET and the SNR1 protein. SNR1 is a product of snr1, which is classified as a trx group gene. We found parallel interaction in yeast between the SET domain of ALL-1 and the human homolog of SNR1, INI1 (hSNF5). These results were confirmed by in vitro binding studies and by demonstrating coimmunoprecipitation of the proteins from cultured cells and/or transgenic flies. Epitope-tagged SNR1 was detected at discrete sites on larval salivary gland polytene chromosomes, and these sites colocalized with around one-half of TRX binding sites. Because SNR1 and INI1 are constituents of the SWI/SNF complex, which acts to remodel chromatin and consequently to activate transcription, the interactions we observed suggest a mechanism by which the SWI/SNF complex is recruited to ALL-1/trx targets through physical interactions between the C-terminal domains of ALL-1 and TRX and INI1/SNR1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Biological Evolution
  • Cell Line
  • Chromosomal Proteins, Non-Histone
  • Cloning, Molecular
  • Conserved Sequence
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Drosophila Proteins*
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Leukemia
  • Myeloid-Lymphoid Leukemia Protein
  • Proto-Oncogenes*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • SMARCB1 Protein
  • Transcription Factors / metabolism*
  • Transfection
  • Tumor Cells, Cultured
  • Zinc Fingers

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Drosophila Proteins
  • KMT2A protein, human
  • Recombinant Proteins
  • SMARCB1 Protein
  • SMARCB1 protein, human
  • Snr1 protein, Drosophila
  • Transcription Factors
  • Trl protein, Drosophila
  • Myeloid-Lymphoid Leukemia Protein
  • Histone-Lysine N-Methyltransferase