The Multi-zinc Finger Protein ZNF217 Contacts DNA through a Two-finger Domain

Nunez, Noelia; Clifton, Molly M.K.; Funnell, Alister P. W.; Artuz, Crisbel M.; Hallal, Samantha; Quinlan, Kate; Font, Josep; Vandevenne, Marylène; Setiyaputra, Surya; Pearson, Richard; Mackay, Joel P.; Crossley, Merlin

doi:10.1074/jbc.m111.301234

Cited by 25 publications

(32 citation statements)

References 63 publications

(41 reference statements)

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“…4). As shown previously (34), substantial chemical shift changes are observed following the addition of WT DNA, and these changes are consistent overall with the structure of the complex. Fig.…”

Section: Znf217 Recognizes Its Cognate Dna Sequence Using a Unique Insupporting

confidence: 66%

“…Our measurements indicated that a GST fusion of ZNF217_F67 recognizes the WT DNA sequence with a relatively low affinity (K d ϭ 130 nM). Even more surprisingly, the affinity was reduced by only 2.5-fold when the core recognition sequence was extensively mutated (from TGCAGAAT to CTGGAGTA) (34). A similar affinity was observed for binding to a poly(AT) sequence (supplemental Fig.…”

Section: Znf217 Recognizes Its Cognate Dna Sequence Using a Unique Insupporting

confidence: 51%

“…Mutation of either of these tyrosines to alanine reduces the affinity of ZNF217 for DNA (34). The weakly polar methyl-interaction has been the subject of debate for some time, and experimental proof of its existence has been demonstrated only very recently (43).…”

Section: Discussionmentioning

confidence: 99%

“…Subsequently, we identified an extended version of this consensus sequence to which stronger binding was observed in gel shifts: namely (T/A)(G/A)CAGAA(T/G/C) (34). Transient transfection experiments in which this sequence was incorporated into a promoter region showed that ZNF217 could act as a transcriptional repressor and that the activity was dependent on the structural integrity of the F67 unit.…”

Section: Zinc Finger (Zf)mentioning

confidence: 99%

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New Insights into DNA Recognition by Zinc Fingers Revealed by Structural Analysis of the Oncoprotein ZNF217

Vandevenne

Jacques

Artuz

et al. 2013

Journal of Biological Chemistry

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Section: Znf217 Recognizes Its Cognate Dna Sequence Using a Unique Insupporting

confidence: 66%

Section: Znf217 Recognizes Its Cognate Dna Sequence Using a Unique Insupporting

confidence: 51%

Section: Discussionmentioning

confidence: 99%

Section: Zinc Finger (Zf)mentioning

confidence: 99%

See 2 more Smart Citations

New Insights into DNA Recognition by Zinc Fingers Revealed by Structural Analysis of the Oncoprotein ZNF217

Vandevenne

Jacques

Artuz

et al. 2013

Journal of Biological Chemistry

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“…Fluorescence polarization measurements were carried out as previously described (Nunez et al, 2011, Rossi & Taylor, 2011 at 25°C on a PHERAstar© FS microplate reader (BMG). The 6-carboxyfluorescein (FAM)-labelled dsDNA probes (2nM) were incubated for 20 min with increasing amounts of protein in 50mM Tris-HCl (pH8.0), 150mM NaCl, 200mM Glutathione-reduced, 50μM ZnCl2, 5mM TCEP, 10% NP-40.…”

Section: Fluorescent Polarisationmentioning

confidence: 99%

Investigating the Molecular Pathogenesis of Inherited Childhood Anaemia

Ilsley¹

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Krüppel-like factors (KLFs) are a group of 17 transcription factors with diverse functions such as early embryo patterning, organogenesis and tissue homoeostasis. All 17 members contain highlyconserved DNA-binding domains consisting of three C-terminal C2H2-type zinc fingers. This high level of conservation allows all members of the KLF family to bind to a 9 base pair CACCC-box DNA sequence (CCM CRC CCN) which is commonly found in many tissue-specific gene promoters and enhancers. The activity of each member of the KLF family is largely determined by a more variable N-terminal domain through which they interact with co-factors such as p300 and C-terminal binding protein 2 (CtBP2).Many KLFs are often expressed in the same cells. In these situations, they can form transcriptional networks where they coordinate to control developmental programs. For example, KLF2, KLF4, and KLF5 work redundantly in embryonic stem cells where they regulate key pluripotency genes such as Nanog to maintain the 'stemness' of the cell. Multiple KLFs are expressed during erythropoiesis, the ongoing production of red blood cells, where it is likely that they form transcriptional networks to control differentiation.Krüppel-like factor 1 (KLF1) is an erythroid-specific transcription factor that is responsible for coordinating the expression of a large cohort of genes required for nearly all aspects of erythropoiesis. As the founding member of the KLF group, KLF1 contains three C-terminal C2H2-type zinc fingers that bind to DNA and an N-terminal proline-rich activation domain that interacts with co-factors to initiate transcription of target genes.This thesis investigates the molecular mechanisms of Klf1 binding specificity to DNA and how this is affected by mutations, and by competition between family members.A disease that is known as Congenital Dyserythropoietic anaemia type IV (CDAIV) is a rare autosomal-dominant inherited erythrocyte disorder characterised by ineffective erythropoiesis and haemolysis. CDAIV is caused by a point mutation in the second zinc finger of KLF1 which results in substitution of an amino acid predicted to bind to DNA.A mouse carrying a point mutation in the corresponding amino acid residue in murine Klf1 to that mutated in CDAIV patients has been previously generated in an ENU screen. This mouse displays a semi-dominant haemolytic anaemia and is named 'Nan' for 'neonatal anaemia'. The Nan mouse shares a similar phenotype to that of patients with CDAIV and hereditary spherocytosis.Incredibly, both the 'Nan' and CDAIV mutations cause disease which is far more severe than that of commonly occurring Klf1 haploinsufficiency.ii ChIP-seq analysis in cell lines developed to model Klf1 mutations identified aberrant DNAbinding events genome-wide for both the mouse 'Nan' mutation and the human CDAIV mutation.Next-generation sequencing of newly-synthesised RNA (4sU-RNA-seq) reveals ectopic transcriptional consequences of this aberrant binding. Novel sequence specificity of the mutant protein was confirmed by performi...

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