PU.1 is a hematopoietic transcription factor belonging to the Ets family of proteins. It regulates transcription of genes specific to lymphoid cells, ultimately leading to cellular differentiation.[1] This transcription factor binds DNA with its helix-turn-helix motif, a common motif in transcription factors and DNA repair proteins.[2]
Function
Within the nucleus, PU.1 activates transcription of lymphoid genes by binding DNA during hematopoiesis. The name PU.1 comes from the protein's binding interactions with a purine-rich DNA sequence.
Activation
A post-translational modification of PU.1 occurs at serine residues, specifically, residues 140 and 146.[3] An experimental study also identified phosphorylation of serine 41 as a modification that induces activity. This phosphorylation is performed by protein kinase B (AKT).[4]
Binding Domain
Ets binding domain is conserved across the Ets family of proteins which consist of about 35 proteins with similar functions.
Binding domain is positively charged. Residues most closely interacting with DNA include Arginine and Lysine. These are highly conserved- the two Arginines on the central helix within the major groove of the DNA and two Lysines on the outer turns.[5]
Disease
PU.1 has been identified as an oncogene. Mutations have been identified in patients with leukemias and lymphomas. Interestingly, the mutations are not always identified within the binding site.
PEST domain
The PEST domain is adjacent to the binding domain and has been found mutated in leukemia patients.[6] It is highly polar due to the abundance of proline, glutamate, serine, and threonine. Proteins with a PEST region typically have a short half-life of under 2 hours. It is hypothesized that the PEST region is a tag for fast degradation of the protein.
Hydration Is Essential to PU.1/DNA Interaction
Water mediates the binding of PU.1 to DNA. As betaine was titrated into a solution of PU.1 and DNA, binding significantly decreased.
References
- ↑ UniProt ConsortiumEuropean Bioinformatics InstituteProtein Information ResourceSIB Swiss Institute of Bioinformatics. (2021, April 7). Transcription factor PU.1. UniProt ConsortiumEuropean Bioinformatics InstituteProtein Information ResourceSIB Swiss Institute of Bioinformatics. https://www.uniprot.org/uniprot/P17947.
- ↑ ARAVIND, L., ANANTHARAMAN, V., BALAJI, S., BABU, M., & IYER, L. (2005). The many faces of the helix-turn-helix domain: Transcription regulation and beyond. FEMS Microbiology Reviews, 29(2), 231–262. https://doi.org/10.1016/j.femsre.2004.12.008
- ↑ UniProt ConsortiumEuropean Bioinformatics InstituteProtein Information ResourceSIB Swiss Institute of Bioinformatics. (2021, April 7). Transcription factor PU.1. UniProt ConsortiumEuropean Bioinformatics InstituteProtein Information ResourceSIB Swiss Institute of Bioinformatics. https://www.uniprot.org/uniprot/P17947.
- ↑ Rieske, P., & Pongubala, J. M. R. (2001). AKT Induces Transcriptional Activity of PU.1 through Phosphorylation-mediated Modifications within Its Transactivation Domain. Journal of Biological Chemistry, 276(11), 8460–8468. https://doi.org/10.1074/jbc.m007482200
- ↑ Kodandapani, R., Pio, F., Ni, CZ. et al. A new pattern for helix–turn–helix recognition revealed by the PU.l ETS–domain–DNA complex. Nature 380, 456–460 (1996). https://doi.org/10.1038/380456a0
- ↑ Mueller, B. U. Heterozygous PU.1 Mutations Are Associated with Acute
Myeloid Leukemia. Blood. 2003, 101(5), 2074–2074.
