Investigating the Molecular Pathogenesis of Inherited Childhood Anaemia
Author(s) -
Melissa Ilsley
Publication year - 2017
Publication title -
queensland's institutional digital repository (the university of queensland)
Language(s) - English
Resource type - Dissertations/theses
DOI - 10.14264/uql.2017.898
Subject(s) - transcription factor , zinc finger , gata1 , biology , gata4 , gata2 , erythropoiesis , enhancer , dna binding domain , genetics , promoter , gene , homeobox protein nanog , microbiology and biotechnology , induced pluripotent stem cell , embryonic stem cell , gene expression , medicine , anemia
The rules of engagement between zinc finger transcription factors and DNA have been partly defined by in vitro DNA-binding and structural studies, but less is known about how these rules apply in vivo. Here we demonstrate how a missense mutation in the second zinc finger of Krüppel-like factor-1 (KLF1) leads to degenerate DNA-binding specificity in vivo, resulting in ectopic transcription and anaemia in the Nan mouse model. We employed ChIP-seq and 4sU-RNA-seq to identify aberrant DNA-binding events genome wide and ectopic transcriptional consequences of this binding. We confirmed novel sequence specificity of the mutant recombinant zinc finger domain by performing biophysical measurements of in vitro DNA-binding affinity. Together, these results shed new light on the mechanisms by which missense mutations in DNA-binding domains of transcription factors can lead to autosomal dominant diseases. Chapter 3: Mutations in the DNA-binding domain of KLF1
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