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Molecular evolution of the homeodomain family of transcription factors

Molecular evolution of the homeodomain family of transcription factors

http://www.wikidata.org/entity/Q33941060

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The homeodomain complement of the ctenophore Mnemiopsis leidyi suggests that Ctenophora and Porifera diverged prior to the ParaHoxozoa Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype Diversity, phylogeny and expression patterns of Pou and Six homeodomain transcription factors in hydrozoan jellyfish Craspedacusta sowerbyi Analysis of homeodomain specificities allows the family-wide prediction of preferred recognition sites NOBOX homeobox mutation causes premature ovarian failure Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome The DNA-binding region of RAG 1 is not a homeodomain.The EH1 motif in metazoan transcription factors Crystal structures of engrailed homeodomain mutants: implications for stability and dynamics Structural basis for homeodomain recognition by the cell-cycle regulator Geminin Investigation of Homeodomain Membrane Translocation Properties: Insights from the Structure Determination of Engrailed-2 Homeodomain in Aqueous and Membrane-Mimetic Environments Limb malformations and the human HOX genes A contracted DNA repeat in LHX3 intron 5 is associated with aberrant splicing and pituitary dwarfism in German shepherd dogs LHX3 interacts with inhibitor of histone acetyltransferase complex subunits LANP and TAF-1β to modulate pituitary gene regulation The cnidarian-bilaterian ancestor possessed at least 56 homeoboxes: evidence from the starlet sea anemone, Nematostella vectensis Rapid evolution of mammalian X-linked testis-expressed homeobox genes Hox, ParaHox, ProtoHox: facts and guesses Classification and nomenclature of all human homeobox genes.Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.A phage display selection of engrailed homeodomain mutants and the importance of residue Q50.The early ANTP gene repertoire: insights from the placozoan genome.Are Hox genes ancestrally involved in axial patterning? Evidence from the hydrozoan Clytia hemisphaerica (Cnidaria).Construction and clarification of dynamic gene regulatory network of cancer cell cycle via microarray data.Coordinated spatial and temporal expression of Hox genes during embryogenesis in the acoel Convolutriloba longifissura.20ns molecular dynamics simulation of the antennapedia homeodomain-DNA complex: water interaction and DNA structure analysis.A non-tree-based comprehensive study of metazoan Hox and ParaHox genes prompts new insights into their origin and evolution Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E.A homeobox protein Phx1 regulates long-term survival and meiotic sporulation in Schizosaccharomyces pombe.Global expression profiling of transcription factor genes provides new insights into pathogenicity and stress responses in the rice blast fungus The RNA binding domain of Jerky consists of tandemly arranged helix-turn-helix/homeodomain-like motifs and binds specific sets of mRNAs A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency.The homeodomain transcription factors antennapedia and POU-M2 regulate the transcription of the steroidogenic enzyme gene Phantom in the silkworm.Karyopherins in nuclear transport of homeodomain proteins during development.CYP2C9 promoter region single-nucleotide polymorphisms linked to the R150H polymorphism are functional suggesting their role in CYP2C9*8-mediated effects SHOX at a glance: from gene to protein.Predicting the binding preference of transcription factors to individual DNA k-mers.PRH/Hex: an oligomeric transcription factor and multifunctional regulator of cell fate.Dynamic Local Polymorphisms in the Gbx1 Homeodomain Induced by DNA Binding.Beyond Hox: the role of ParaHox genes in normal and malignant hematopoiesis Proteins Recognizing DNA: Structural Uniqueness and Versatility of DNA-Binding Domains in Stem Cell Transcription Factors.

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P2860

Molecular evolution of the homeodomain family of transcription factors

http://www.wikidata.org/entity/Q33941060

description

2001 nî lūn-bûn

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2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2001 թվականի օգոստոսին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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Molecular evolution of the homeodomain family of transcription factors

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Molecular evolution of the homeodomain family of transcription factors

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Molecular evolution of the homeodomain family of transcription factors

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Molecular evolution of the homeodomain family of transcription factors

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prefLabel

Molecular evolution of the homeodomain family of transcription factors

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Molecular evolution of the homeodomain family of transcription factors

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Nucleic Acids Research

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Molecular evolution of the homeodomain family of transcription factors

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A D Baxevanis

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S Banerjee-Basu

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P2860

Initial sequencing and analysis of the human genome

Structure of a HoxB1-Pbx1 heterodimer bound to DNA: role of the hexapeptide and a fourth homeodomain helix in complex formation

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease

Isolation and mapping of EVX1, a human homeobox gene homologous to even-skipped, localized at the 5' end of HOX1 locus on chromosome 7

Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome

Congenital heart disease caused by mutations in the transcription factor NKX2-5

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

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10.1093/NAR/29.15.3258

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