Literature DB >> 24218595

Hox5 interacts with Plzf to restrict Shh expression in the developing forelimb.

Ben Xu1, Steven M Hrycaj, Daniel C McIntyre, Nicholas C Baker, Jun K Takeuchi, Lucie Jeannotte, Zachary B Gaber, Bennett G Novitch, Deneen M Wellik.   

Abstract

To date, only the five most posterior groups of Hox genes, Hox9-Hox13, have demonstrated loss-of-function roles in limb patterning. Individual paralog groups control proximodistal patterning of the limb skeletal elements. Hox9 genes also initiate the onset of Hand2 expression in the posterior forelimb compartment, and collectively, the posterior HoxA/D genes maintain posterior Sonic Hedgehog (Shh) expression. Here we show that an anterior Hox paralog group, Hox5, is required for forelimb anterior patterning. Deletion of all three Hox5 genes (Hoxa5, Hoxb5, and Hoxc5) leads to anterior forelimb defects resulting from derepression of Shh expression. The phenotype requires the loss of all three Hox5 genes, demonstrating the high level of redundancy in this Hox paralogous group. Further analyses reveal that Hox5 interacts with promyelocytic leukemia zinc finger biochemically and genetically to restrict Shh expression. These findings, along with previous reports showing that point mutations in the Shh limb enhancer lead to similar anterior limb defects, highlight the importance of Shh repression for proper patterning of the vertebrate limb.

Entities:  

Keywords:  anteroposterior limb patterning; gene interactions; limb development; mouse developmental genetics; organogenesis

Mesh:

Substances:

Year:  2013        PMID: 24218595      PMCID: PMC3845161          DOI: 10.1073/pnas.1315075110

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  59 in total

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Authors:  P Bourgeois; A L Bolcato-Bellemin; J M Danse; A Bloch-Zupan; K Yoshiba; C Stoetzel; F Perrin-Schmitt
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Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

3.  Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.

Authors:  Q Y Li; R A Newbury-Ecob; J A Terrett; D I Wilson; A R Curtis; C H Yi; T Gebuhr; P J Bullen; S C Robson; T Strachan; D Bonnet; S Lyonnet; I D Young; J A Raeburn; A J Buckler; D J Law; J D Brook
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

4.  Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb.

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Journal:  Development       Date:  2005-02       Impact factor: 6.868

5.  Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations.

Authors:  C T Basson; T Huang; R C Lin; D R Bachinsky; S Weremowicz; A Vaglio; R Bruzzone; R Quadrelli; M Lerone; G Romeo; M Silengo; A Pereira; J Krieger; S F Mesquita; M Kamisago; C C Morton; M E Pierpont; C W Müller; J G Seidman; C E Seidman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

6.  Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.

Authors:  J Kohlhase; A Wischermann; H Reichenbach; U Froster; W Engel
Journal:  Nat Genet       Date:  1998-01       Impact factor: 38.330

7.  Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36.

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8.  Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.

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Journal:  Am J Hum Genet       Date:  2002-10-22       Impact factor: 11.025

9.  Early developmental arrest of mammalian limbs lacking HoxA/HoxD gene function.

Authors:  Marie Kmita; Basile Tarchini; Jozsef Zàkàny; Malcolm Logan; Clifford J Tabin; Denis Duboule
Journal:  Nature       Date:  2005-06-23       Impact factor: 49.962

10.  Hoxd-12 differentially affects preaxial and postaxial chondrogenic branches in the limb and regulates Sonic hedgehog in a positive feedback loop.

Authors:  V Knezevic; R De Santo; K Schughart; U Huffstadt; C Chiang; K A Mahon; S Mackem
Journal:  Development       Date:  1997-11       Impact factor: 6.868

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  18 in total

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Authors:  Kyriel M Pineault; Deneen M Wellik
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2.  Hox5 genes direct elastin network formation during alveologenesis by regulating myofibroblast adhesion.

Authors:  Steven M Hrycaj; Leilani Marty-Santos; Cristina Cebrian; Andrew J Rasky; Catherine Ptaschinski; Nicholas W Lukacs; Deneen M Wellik
Journal:  Proc Natl Acad Sci U S A       Date:  2018-10-22       Impact factor: 11.205

Review 3.  The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.

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4.  Identification of Novel EZH2 Targets Regulating Osteogenic Differentiation in Mesenchymal Stem Cells.

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6.  Pigeon foot feathering reveals conserved limb identity networks.

Authors:  Elena F Boer; Hannah F Van Hollebeke; Sungdae Park; Carlos R Infante; Douglas B Menke; Michael D Shapiro
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7.  Hox5 Genes Regulate the Wnt2/2b-Bmp4-Signaling Axis during Lung Development.

Authors:  Steven M Hrycaj; Briana R Dye; Nicholas C Baker; Brian M Larsen; Ann C Burke; Jason R Spence; Deneen M Wellik
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Review 8.  How the embryo makes a limb: determination, polarity and identity.

Authors:  Cheryll Tickle
Journal:  J Anat       Date:  2015-08-07       Impact factor: 2.610

9.  Mesenchymal Hox6 function is required for mouse pancreatic endocrine cell differentiation.

Authors:  Brian M Larsen; Steven M Hrycaj; Micaleah Newman; Ye Li; Deneen M Wellik
Journal:  Development       Date:  2015-10-08       Impact factor: 6.868

10.  HOXA5 protein expression and genetic fate mapping show lineage restriction in the developing musculoskeletal system.

Authors:  Miriam A Holzman; Jenna M Bergmann; Maya Feldman; Kim Landry-Truchon; Lucie Jeannotte; Jennifer H Mansfield
Journal:  Int J Dev Biol       Date:  2018       Impact factor: 2.203

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