Proteolytic cleavage of MLL generates a complex of N- and C-terminal fragments that confers protein stability and subnuclear localization Journal Article
| Authors: | Hsieh, J. J. D.; Ernst, P.; Erdjument-Bromage, H.; Tempst, P.; Korsmeyer, S. J. |
| Article Title: | Proteolytic cleavage of MLL generates a complex of N- and C-terminal fragments that confers protein stability and subnuclear localization |
| Abstract: | The mixed-lineage leukemia gene (MLL, ALL1, HRX) encodes a 3,969-amino-acid nuclear protein homologous to Drosophila trithorax and is required to maintain proper Hox gene expression. Chromosome translocations in human leukemia disrupt MLL (11q23), generating chimeric proteins between the N terminus of MLL and multiple translocation partners. Here we report that MLL is normally cleaved at two conserved sites (D/GADD and D/GVDD) and that mutation of these sites abolishes the proteolysis. MLL cleavage generates N-terminal p320 (N320) and C-terminal p180 (C180) fragments, which form a stable complex that localizes to a subnuclear compartment. The FYRN domain of N320 directly interacts with the FYRC and SET domains of C180. Disrupting the interaction between N320 and C180 leads to a marked decrease in the level of N320 and a redistribution of C180 to a diffuse nuclear pattern. These data suggest a model in which a dynamic post-cleavage association confers stability to N320 and correct nuclear sublocalization of the complex, to control the availability of N320 for target genes. This predicts that MLL fusion proteins of leukemia which would lose the ability to complex with C180 have their stability conferred instead by the fusion partners, thus providing one mechanism for altered target gene expression. |
| Keywords: | human cell; mutation; dna-binding proteins; nonhuman; protein domain; protein localization; cells, cultured; complex formation; gene expression; carboxy terminal sequence; protein degradation; protein protein interaction; protein stability; drosophila; transcription factors; amino acid sequence; conserved sequence; amino terminal sequence; peptide fragments; recombinant proteins; chromosome translocation; amino acid; protein structure, tertiary; sequence homology; chromosome 11q; amino acid motifs; proto-oncogenes; mixed lineage leukemia protein; myeloid-lymphoid leukemia protein; hox gene; cell nucleus structures; humans; human; priority journal; article; drosophila trithorax |
| Journal Title: | Molecular and Cellular Biology |
| Volume: | 23 |
| Issue: | 1 |
| ISSN: | 0270-7306 |
| Publisher: | American Society for Microbiology |
| Date Published: | 2003-01-01 |
| Start Page: | 186 |
| End Page: | 194 |
| Language: | English |
| DOI: | 10.1128/mcb.23.1.186-194.2003 |
| PUBMED: | 12482972 |
| PROVIDER: | scopus |
| PMCID: | PMC140678 |
| DOI/URL: | |
| Notes: | Export Date: 12 September 2014 -- Source: Scopus |
