Literature DB >> 15726414

Homeodomain revisited: a lesson from disease-causing mutations.

Young-In Chi1.   

Abstract

The homeodomain is a highly conserved DNA-binding motif that is found in numerous transcription factors throughout a large variety of species from yeast to humans. These gene-specific transcription factors play critical roles in development and adult homeostasis, and therefore, any germline mutations associated with these proteins can lead to a number of congenital abnormalities. Although much has been revealed concerning the molecular architecture and the mechanism of homeodomain-DNA interactions, the study of disease-causing mutations can further provide us with instructive information as to the role of particular residues in a conserved mode of action. In this paper, I have compiled the homeodomain missense mutations found in various human diseases and re-examined the functional role of the mutational "hot spot" residues in light of the structures obtained from crystallography. These findings should be useful in understanding the essential components of the homeodomain and in attempts to design agonist or antagonists to modulate their activity and to reverse the effects caused by the mutations.

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Year:  2005        PMID: 15726414      PMCID: PMC1579204          DOI: 10.1007/s00439-004-1252-1

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  61 in total

1.  High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA.

Authors:  D S Wilson; B Guenther; C Desplan; J Kuriyan
Journal:  Cell       Date:  1995-09-08       Impact factor: 41.582

2.  Site-directed mutations in the vnd/NK-2 homeodomain. Basis of variations in structure and sequence-specific DNA binding.

Authors:  S Weiler; J M Gruschus; D H Tsao; L Yu; L H Wang; M Nirenberg; J A Ferretti
Journal:  J Biol Chem       Date:  1998-05-01       Impact factor: 5.157

Review 3.  Homeodomain interactions.

Authors:  C Wolberger
Journal:  Curr Opin Struct Biol       Date:  1996-02       Impact factor: 6.809

Review 4.  POU domain family values: flexibility, partnerships, and developmental codes.

Authors:  A K Ryan; M G Rosenfeld
Journal:  Genes Dev       Date:  1997-05-15       Impact factor: 11.361

5.  Structure of Pit-1 POU domain bound to DNA as a dimer: unexpected arrangement and flexibility.

Authors:  E M Jacobson; P Li; A Leon-del-Rio; M G Rosenfeld; A K Aggarwal
Journal:  Genes Dev       Date:  1997-01-15       Impact factor: 11.361

6.  Mutations in PROP1 cause familial combined pituitary hormone deficiency.

Authors:  W Wu; J D Cogan; R W Pfäffle; J S Dasen; H Frisch; S M O'Connell; S E Flynn; M R Brown; P E Mullis; J S Parks; J A Phillips; M G Rosenfeld
Journal:  Nat Genet       Date:  1998-02       Impact factor: 38.330

7.  Engrailed (Gln50-->Lys) homeodomain-DNA complex at 1.9 A resolution: structural basis for enhanced affinity and altered specificity.

Authors:  L Tucker-Kellogg; M A Rould; K A Chambers; S E Ades; R T Sauer; C O Pabo
Journal:  Structure       Date:  1997-08-15       Impact factor: 5.006

8.  Homeodomain determinants of major groove recognition.

Authors:  J L Pomerantz; P A Sharp
Journal:  Biochemistry       Date:  1994-09-13       Impact factor: 3.162

9.  Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.

Authors:  M T Dattani; J P Martinez-Barbera; P Q Thomas; J M Brickman; R Gupta; I L Mårtensson; H Toresson; M Fox; J K Wales; P C Hindmarsh; S Krauss; R S Beddington; I C Robinson
Journal:  Nat Genet       Date:  1998-06       Impact factor: 38.330

Review 10.  Transcription factors in disease.

Authors:  D Engelkamp; V van Heyningen
Journal:  Curr Opin Genet Dev       Date:  1996-06       Impact factor: 5.578

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  28 in total

1.  Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.

Authors:  Elif Uz; Yasemin Alanay; Dilek Aktas; Ibrahim Vargel; Safak Gucer; Gokhan Tuncbilek; Ferdinand von Eggeling; Engin Yilmaz; Ozgur Deren; Nicole Posorski; Hilal Ozdag; Thomas Liehr; Sevim Balci; Mehmet Alikasifoglu; Bernd Wollnik; Nurten A Akarsu
Journal:  Am J Hum Genet       Date:  2010-05-06       Impact factor: 11.025

2.  HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

Authors:  Bryn D Webb; Sherin Shaaban; Harald Gaspar; Luis F Cunha; Christian R Schubert; Ke Hao; Caroline D Robson; Wai-Man Chan; Caroline Andrews; Sarah MacKinnon; Darren T Oystreck; David G Hunter; Anthony J Iacovelli; Xiaoqian Ye; Anne Camminady; Elizabeth C Engle; Ethylin Wang Jabs
Journal:  Am J Hum Genet       Date:  2012-07-05       Impact factor: 11.025

3.  Dynamic Local Polymorphisms in the Gbx1 Homeodomain Induced by DNA Binding.

Authors:  Andrew Proudfoot; Michael Geralt; Marc-Andre Elsliger; Ian A Wilson; Kurt Wüthrich; Pedro Serrano
Journal:  Structure       Date:  2016-07-07       Impact factor: 5.006

4.  Crystallization of hepatocyte nuclear factor 1beta in complex with DNA.

Authors:  Peng Lu; Yun Li; Amanda Gorman; Young-In Chi
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2006-05-05

5.  Role of conserved salt bridges in homeodomain stability and DNA binding.

Authors:  Mario Torrado; Julia Revuelta; Carlos Gonzalez; Francisco Corzana; Agatha Bastida; Juan Luis Asensio
Journal:  J Biol Chem       Date:  2009-06-26       Impact factor: 5.157

6.  A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

Authors:  Adrianna Mostowska; Barbara Biedziak; Wiesław H Trzeciak
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

7.  Human gene-centered transcription factor networks for enhancers and disease variants.

Authors:  Juan I Fuxman Bass; Nidhi Sahni; Shaleen Shrestha; Aurian Garcia-Gonzalez; Akihiro Mori; Numana Bhat; Song Yi; David E Hill; Marc Vidal; Albertha J M Walhout
Journal:  Cell       Date:  2015-04-23       Impact factor: 41.582

8.  The Homeodomain Resource: a comprehensive collection of sequence, structure, interaction, genomic and functional information on the homeodomain protein family.

Authors:  R Travis Moreland; Joseph F Ryan; Christopher Pan; Andreas D Baxevanis
Journal:  Database (Oxford)       Date:  2009-04-17       Impact factor: 3.451

9.  Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.

Authors:  Cheryl Shoubridge; May Huey Tan; Tod Fullston; Desiree Cloosterman; David Coman; George McGillivray; Grazia M Mancini; Tjitske Kleefstra; Jozef Gécz
Journal:  Pathogenetics       Date:  2010-01-05

10.  Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.

Authors:  Stephen R F Twigg; Sarah L Versnel; Gudrun Nürnberg; Melissa M Lees; Meenakshi Bhat; Peter Hammond; Raoul C M Hennekam; A Jeannette M Hoogeboom; Jane A Hurst; David Johnson; Alexis A Robinson; Peter J Scambler; Dianne Gerrelli; Peter Nürnberg; Irene M J Mathijssen; Andrew O M Wilkie
Journal:  Am J Hum Genet       Date:  2009-04-30       Impact factor: 11.025

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