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Purification and characterization of polyhomeotic associated proteins from Drosophila Kc1 cells Wang, Yong-Jun
Abstract
The Polycomb group (PcG) genes encode repressors of homeotic and other genes, that are required to maintain silencing of target loci. Tethered P cG proteins repress reporter genes in cell lines and in Drosophila embryos, showing that P cG proteins are repressors. PcG genes are required for the maintenance but not the initiation of homeotic gene repression, because in P cG mutants, initiation of homeotic gene expression is normal, and then breaks down after a lag of several hours. Coimmunoprecipitation and cofractionation of P cG proteins, colocalization of P cG proteins on polytene chromosomes, and synergistic mutant phenotypes in double heterozygous mutants of PcG genes suggest that P cG proteins act through multimeric protein complexes. However, the mechanisms of PcG-mediated homeotic gene silencing are not known. One approach to this problem is to identify proteins that associate with PcG proteins in vivo in an effort to generate testable hypotheses about PcG-mediated silencing. Using epitope tagging followed by immunopurification, I purified Polyhomeotic (PH) proximal and its associated proteins from Drosophila K c l cell nuclear extracts. I subsequently identified the PH-associated proteins using mass spectrometry sequencing and western blotting analysis. I showed that molecular chaperones are associated with P H and that a mutation in chaperone Hsc70.4 enhances the extra sex combs phenotype of ph and Pc. These results suggest that chaperones may participate in the formation of PH-containing complexes, or may be required for silencing. I demonstrated that the histone deacetylase Rpd3 and histone binding protein p55 are associated with PH, and that the Rpd3 mutation enhances the extra sex combs phenotype of ph and Pc. Surprisingly, histone deacetylase activity was not detected in immunopurified PH. I showed using western blotting analysis that the TATA-binding protein (TBP) and its associating proteins TAFn 4 2 and TAFn85 are also associated with PH. PH and PC were coimmunoprecipitated by anti- TBP antibody. In addition, Tbp mutants enhance the extra sex combs phenotype of ph but not Pc. Together, these findings suggest that P cG proteins use different means to silence gene expression including modifying histones and targeting the basal transcriptional machinery.
Item Metadata
Title |
Purification and characterization of polyhomeotic associated proteins from Drosophila Kc1 cells
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Creator | |
Publisher |
University of British Columbia
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Date Issued |
2003
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Description |
The Polycomb group (PcG) genes encode repressors of homeotic and other genes,
that are required to maintain silencing of target loci. Tethered P cG proteins repress
reporter genes in cell lines and in Drosophila embryos, showing that P cG proteins are
repressors. PcG genes are required for the maintenance but not the initiation of homeotic
gene repression, because in P cG mutants, initiation of homeotic gene expression is
normal, and then breaks down after a lag of several hours. Coimmunoprecipitation and
cofractionation of P cG proteins, colocalization of P cG proteins on polytene
chromosomes, and synergistic mutant phenotypes in double heterozygous mutants of PcG
genes suggest that P cG proteins act through multimeric protein complexes. However, the
mechanisms of PcG-mediated homeotic gene silencing are not known. One approach to
this problem is to identify proteins that associate with PcG proteins in vivo in an effort to
generate testable hypotheses about PcG-mediated silencing. Using epitope tagging
followed by immunopurification, I purified Polyhomeotic (PH) proximal and its
associated proteins from Drosophila K c l cell nuclear extracts. I subsequently identified
the PH-associated proteins using mass spectrometry sequencing and western blotting
analysis. I showed that molecular chaperones are associated with P H and that a mutation
in chaperone Hsc70.4 enhances the extra sex combs phenotype of ph and Pc. These
results suggest that chaperones may participate in the formation of PH-containing
complexes, or may be required for silencing. I demonstrated that the histone deacetylase
Rpd3 and histone binding protein p55 are associated with PH, and that the Rpd3 mutation
enhances the extra sex combs phenotype of ph and Pc. Surprisingly, histone deacetylase
activity was not detected in immunopurified PH. I showed using western blotting
analysis that the TATA-binding protein (TBP) and its associating proteins TAFn 4 2 and
TAFn85 are also associated with PH. PH and PC were coimmunoprecipitated by anti-
TBP antibody. In addition, Tbp mutants enhance the extra sex combs phenotype of ph
but not Pc. Together, these findings suggest that P cG proteins use different means to
silence gene expression including modifying histones and targeting the basal
transcriptional machinery.
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Extent |
16175660 bytes
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Genre | |
Type | |
File Format |
application/pdf
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Language |
eng
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Date Available |
2009-09-26
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Provider |
Vancouver : University of British Columbia Library
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Rights |
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
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DOI |
10.14288/1.0090643
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URI | |
Degree | |
Program | |
Affiliation | |
Degree Grantor |
University of British Columbia
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Graduation Date |
2002-05
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Campus | |
Scholarly Level |
Graduate
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Aggregated Source Repository |
DSpace
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Rights
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.