Molecular analysis of the interaction between the hematopoietic master transcription factors GATA-1 and PU.1.

Chu Wai Liew; Kasper Dyrberg Rand; Raina J Y Simpson; Wendy W Yung; Robyn E Mansfield; Merlin Crossley; Mette Proetorius-Ibba; Claus Nerlov; Flemming M Poulsen; Joel P Mackay

doi:10.1074/jbc.M602830200

Molecular analysis of the interaction between the hematopoietic master transcription factors GATA-1 and PU.1.

Chu Wai Liew, Kasper Dyrberg Rand, Raina J Y Simpson, Wendy W Yung, Robyn E Mansfield, Merlin Crossley, Mette Proetorius-Ibba, Claus Nerlov, Flemming M Poulsen, Joel P Mackay

Biomolecular Sciences

43 Citations (Scopus)

Abstract

GATA-1 and PU.1 are transcription factors that control erythroid and myeloid development, respectively. The two proteins have been shown to function in an antagonistic fashion, with GATA-1 repressing PU.1 activity during erythropoiesis and PU.1 repressing GATA-1 function during myelopoiesis. It has also become clear that this functional antagonism involves direct interactions between the two proteins. However, the molecular basis for these interactions is not known, and a number of inconsistencies exist in the literature. We have used a range of biophysical methods to define the molecular details of the GATA-1-PU.1 interaction. A combination of NMR titration data and extensive mutagenesis revealed that the PU.1-Ets domain and the GATA-1 C-terminal zinc finger (CF) form a low affinity interaction in which specific regions of each protein are implicated. Surprisingly, the interaction cannot be disrupted by single alanine substitution mutations, suggesting that binding is distributed over an extended interface. The C-terminal basic tail region of CF appears to be sufficient to mediate an interaction with PU.1-Ets, and neither acetylation nor phosphorylation of a peptide corresponding to this region disrupts binding, indicating that the interaction is not dominated by electrostatic interactions. The CF basic tail shares significant sequence homology with the PU.1 interacting motif from c-Jun, suggesting that GATA-1 and c-Jun might compete to bind PU.1. Taken together, our data provide a molecular perspective on the GATA-1-PU.1 interaction, resolving several issues in the existing data and providing insight into the mechanisms through which these two proteins combine to regulate blood development.
Udgivelsesdato: 2006-Sep-22

Original language	English
Journal	Journal of Biological Chemistry
Volume	281
Issue number	38
Pages (from-to)	28296-306
Number of pages	10
ISSN	0021-9258
DOIs	https://doi.org/10.1074/jbc.M602830200
Publication status	Published - 2006

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Cite this

@article{5582b540e9c911dcbee902004c4f4f50,

title = "Molecular analysis of the interaction between the hematopoietic master transcription factors GATA-1 and PU.1.",

abstract = "GATA-1 and PU.1 are transcription factors that control erythroid and myeloid development, respectively. The two proteins have been shown to function in an antagonistic fashion, with GATA-1 repressing PU.1 activity during erythropoiesis and PU.1 repressing GATA-1 function during myelopoiesis. It has also become clear that this functional antagonism involves direct interactions between the two proteins. However, the molecular basis for these interactions is not known, and a number of inconsistencies exist in the literature. We have used a range of biophysical methods to define the molecular details of the GATA-1-PU.1 interaction. A combination of NMR titration data and extensive mutagenesis revealed that the PU.1-Ets domain and the GATA-1 C-terminal zinc finger (CF) form a low affinity interaction in which specific regions of each protein are implicated. Surprisingly, the interaction cannot be disrupted by single alanine substitution mutations, suggesting that binding is distributed over an extended interface. The C-terminal basic tail region of CF appears to be sufficient to mediate an interaction with PU.1-Ets, and neither acetylation nor phosphorylation of a peptide corresponding to this region disrupts binding, indicating that the interaction is not dominated by electrostatic interactions. The CF basic tail shares significant sequence homology with the PU.1 interacting motif from c-Jun, suggesting that GATA-1 and c-Jun might compete to bind PU.1. Taken together, our data provide a molecular perspective on the GATA-1-PU.1 interaction, resolving several issues in the existing data and providing insight into the mechanisms through which these two proteins combine to regulate blood development. Udgivelsesdato: 2006-Sep-22",

author = "Liew, {Chu Wai} and Rand, {Kasper Dyrberg} and Simpson, {Raina J Y} and Yung, {Wendy W} and Mansfield, {Robyn E} and Merlin Crossley and Mette Proetorius-Ibba and Claus Nerlov and Poulsen, {Flemming M} and Mackay, {Joel P}",

note = "Keywords: Acetylation; Amino Acid Motifs; Amino Acid Sequence; Animals; Binding Sites; DNA; GATA1 Transcription Factor; Hematopoiesis; Humans; Mice; Molecular Sequence Data; Phosphorylation; Proto-Oncogene Proteins; Trans-Activators; Zinc Fingers",

year = "2006",

doi = "10.1074/jbc.M602830200",

language = "English",

volume = "281",

pages = "28296--306",

journal = "Journal of Biological Chemistry",

issn = "0021-9258",

publisher = "American Society for Biochemistry and Molecular Biology, Inc.",

number = "38",

}

TY - JOUR

T1 - Molecular analysis of the interaction between the hematopoietic master transcription factors GATA-1 and PU.1.

AU - Liew, Chu Wai

AU - Rand, Kasper Dyrberg

AU - Simpson, Raina J Y

AU - Yung, Wendy W

AU - Mansfield, Robyn E

AU - Crossley, Merlin

AU - Proetorius-Ibba, Mette

AU - Nerlov, Claus

AU - Poulsen, Flemming M

AU - Mackay, Joel P

N1 - Keywords: Acetylation; Amino Acid Motifs; Amino Acid Sequence; Animals; Binding Sites; DNA; GATA1 Transcription Factor; Hematopoiesis; Humans; Mice; Molecular Sequence Data; Phosphorylation; Proto-Oncogene Proteins; Trans-Activators; Zinc Fingers

PY - 2006

Y1 - 2006

N2 - GATA-1 and PU.1 are transcription factors that control erythroid and myeloid development, respectively. The two proteins have been shown to function in an antagonistic fashion, with GATA-1 repressing PU.1 activity during erythropoiesis and PU.1 repressing GATA-1 function during myelopoiesis. It has also become clear that this functional antagonism involves direct interactions between the two proteins. However, the molecular basis for these interactions is not known, and a number of inconsistencies exist in the literature. We have used a range of biophysical methods to define the molecular details of the GATA-1-PU.1 interaction. A combination of NMR titration data and extensive mutagenesis revealed that the PU.1-Ets domain and the GATA-1 C-terminal zinc finger (CF) form a low affinity interaction in which specific regions of each protein are implicated. Surprisingly, the interaction cannot be disrupted by single alanine substitution mutations, suggesting that binding is distributed over an extended interface. The C-terminal basic tail region of CF appears to be sufficient to mediate an interaction with PU.1-Ets, and neither acetylation nor phosphorylation of a peptide corresponding to this region disrupts binding, indicating that the interaction is not dominated by electrostatic interactions. The CF basic tail shares significant sequence homology with the PU.1 interacting motif from c-Jun, suggesting that GATA-1 and c-Jun might compete to bind PU.1. Taken together, our data provide a molecular perspective on the GATA-1-PU.1 interaction, resolving several issues in the existing data and providing insight into the mechanisms through which these two proteins combine to regulate blood development. Udgivelsesdato: 2006-Sep-22

AB - GATA-1 and PU.1 are transcription factors that control erythroid and myeloid development, respectively. The two proteins have been shown to function in an antagonistic fashion, with GATA-1 repressing PU.1 activity during erythropoiesis and PU.1 repressing GATA-1 function during myelopoiesis. It has also become clear that this functional antagonism involves direct interactions between the two proteins. However, the molecular basis for these interactions is not known, and a number of inconsistencies exist in the literature. We have used a range of biophysical methods to define the molecular details of the GATA-1-PU.1 interaction. A combination of NMR titration data and extensive mutagenesis revealed that the PU.1-Ets domain and the GATA-1 C-terminal zinc finger (CF) form a low affinity interaction in which specific regions of each protein are implicated. Surprisingly, the interaction cannot be disrupted by single alanine substitution mutations, suggesting that binding is distributed over an extended interface. The C-terminal basic tail region of CF appears to be sufficient to mediate an interaction with PU.1-Ets, and neither acetylation nor phosphorylation of a peptide corresponding to this region disrupts binding, indicating that the interaction is not dominated by electrostatic interactions. The CF basic tail shares significant sequence homology with the PU.1 interacting motif from c-Jun, suggesting that GATA-1 and c-Jun might compete to bind PU.1. Taken together, our data provide a molecular perspective on the GATA-1-PU.1 interaction, resolving several issues in the existing data and providing insight into the mechanisms through which these two proteins combine to regulate blood development. Udgivelsesdato: 2006-Sep-22

U2 - 10.1074/jbc.M602830200

DO - 10.1074/jbc.M602830200

M3 - Journal article

C2 - 16861236

SN - 0021-9258

VL - 281

SP - 28296

EP - 28306

JO - Journal of Biological Chemistry

JF - Journal of Biological Chemistry

IS - 38

ER -