Restricted leucine zipper dimerization and specificity of DNA recognition of the melanocyte master regulator MITF
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Restricted leucine zipper dimerization and specificity of DNA recognition of the melanocyte master regulator MITF. / Pogenberg, Vivian; Ogmundsdóttir, Margrét H; Bergsteinsdóttir, Kristín; Schepsky, Alexander; Phung, Bengt; Deineko, Viktor; Milewski, Morlin; Steingrímsson, Eiríkur; Wilmanns, Matthias.
in: GENE DEV, Jahrgang 26, Nr. 23, 01.12.2012, S. 2647-58.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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T1 - Restricted leucine zipper dimerization and specificity of DNA recognition of the melanocyte master regulator MITF
AU - Pogenberg, Vivian
AU - Ogmundsdóttir, Margrét H
AU - Bergsteinsdóttir, Kristín
AU - Schepsky, Alexander
AU - Phung, Bengt
AU - Deineko, Viktor
AU - Milewski, Morlin
AU - Steingrímsson, Eiríkur
AU - Wilmanns, Matthias
PY - 2012/12/1
Y1 - 2012/12/1
N2 - Microphthalmia-associated transcription factor (MITF) is a master regulator of melanocyte development and an important oncogene in melanoma. MITF heterodimeric assembly with related basic helix-loop-helix leucine zipper transcription factors is highly restricted, and its binding profile to cognate DNA sequences is distinct. Here, we determined the crystal structure of MITF in its apo conformation and in the presence of two related DNA response elements, the E-box and M-box. In addition, we investigated mouse and human Mitf mutations to dissect the functional significance of structural features. Owing to an unusual three-residue shift in the leucine zipper register, the MITF homodimer shows a marked kink in one of the two zipper helices to allow an out-of-register assembly. Removal of this insertion relieves restricted heterodimerization by MITF and permits assembly with the transcription factor MAX. Binding of MITF to the M-box motif is mediated by an unusual nonpolar interaction by Ile212, a residue that is mutated in mice and humans with Waardenburg syndrome. As several related transcription factors have low affinity for the M-box sequence, our analysis unravels how these proteins discriminate between similar target sequences. Our data provide a rational basis for targeting MITF in the treatment of important hereditary diseases and cancer.
AB - Microphthalmia-associated transcription factor (MITF) is a master regulator of melanocyte development and an important oncogene in melanoma. MITF heterodimeric assembly with related basic helix-loop-helix leucine zipper transcription factors is highly restricted, and its binding profile to cognate DNA sequences is distinct. Here, we determined the crystal structure of MITF in its apo conformation and in the presence of two related DNA response elements, the E-box and M-box. In addition, we investigated mouse and human Mitf mutations to dissect the functional significance of structural features. Owing to an unusual three-residue shift in the leucine zipper register, the MITF homodimer shows a marked kink in one of the two zipper helices to allow an out-of-register assembly. Removal of this insertion relieves restricted heterodimerization by MITF and permits assembly with the transcription factor MAX. Binding of MITF to the M-box motif is mediated by an unusual nonpolar interaction by Ile212, a residue that is mutated in mice and humans with Waardenburg syndrome. As several related transcription factors have low affinity for the M-box sequence, our analysis unravels how these proteins discriminate between similar target sequences. Our data provide a rational basis for targeting MITF in the treatment of important hereditary diseases and cancer.
KW - Amino Acid Sequence
KW - Animals
KW - DNA-Binding Proteins/chemistry
KW - Dimerization
KW - Enhancer Elements, Genetic/genetics
KW - Humans
KW - Leucine Zippers/genetics
KW - Mice
KW - Microphthalmia-Associated Transcription Factor/chemistry
KW - Models, Molecular
KW - Molecular Sequence Data
KW - Mutation
KW - Protein Binding
KW - Protein Structure, Tertiary
KW - Sequence Alignment
KW - Waardenburg Syndrome/genetics
U2 - 10.1101/gad.198192.112
DO - 10.1101/gad.198192.112
M3 - SCORING: Journal article
C2 - 23207919
VL - 26
SP - 2647
EP - 2658
JO - GENE DEV
JF - GENE DEV
SN - 0890-9369
IS - 23
ER -