Literature DB >> 18694563

Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.

Xin Geng1, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver.   

Abstract

Holoprosencephaly (HPE), the most common forebrain malformation, is characterized by an incomplete separation of the cerebral hemispheres. Mutations in the homeobox gene SIX3 account for 1.3% of all cases of human HPE. Using zebrafish-based assays, we have now determined that HPE-associated Six3 mutant proteins function as hypomorphs. Haploinsufficiency of Six3 caused by deletion of one allele of Six3 or by replacement of wild-type Six3 with HPE-associated Six3 mutant alleles was sufficient to recapitulate in mouse models most of the phenotypic features of human HPE. We demonstrate that Shh is a direct target of Six3 in the rostral diencephalon ventral midline (RDVM). Reduced amounts of functional Six3 protein fail to activate Shh expression in the mutant RDVM and ultimately lead to HPE. These results identify Six3 as a direct regulator of Shh expression and reveal a crossregulatory loop between Shh and Six3 in the ventral forebrain.

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Year:  2008        PMID: 18694563      PMCID: PMC2597207          DOI: 10.1016/j.devcel.2008.07.003

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  45 in total

1.  First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations.

Authors:  L Pasquier; C Dubourg; M Gonzales; L Lazaro; V David; S Odent; F Encha-Razavi
Journal:  J Med Genet       Date:  2005-01       Impact factor: 6.318

2.  Emx2 and Pax6 function in cooperation with Otx2 and Otx1 to develop caudal forebrain primordium that includes future archipallium.

Authors:  Jun Kimura; Yoko Suda; Daisuke Kurokawa; Zakir M Hossain; Miwa Nakamura; Maiko Takahashi; Akemi Hara; Shinichi Aizawa
Journal:  J Neurosci       Date:  2005-05-25       Impact factor: 6.167

3.  Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.

Authors:  D E Wallis; E Roessler; U Hehr; L Nanni; T Wiltshire; A Richieri-Costa; G Gillessen-Kaesbach; E H Zackai; J Rommens; M Muenke
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

4.  Molecular interactions coordinating the development of the forebrain and face.

Authors:  Ralph S Marcucio; Dwight R Cordero; Diane Hu; Jill A Helms
Journal:  Dev Biol       Date:  2005-08-01       Impact factor: 3.582

5.  Expression of murine Lhx5 suggests a role in specifying the forebrain.

Authors:  H Z Sheng; S Bertuzzi; C Chiang; W Shawlot; M Taira; I Dawid; H Westphal
Journal:  Dev Dyn       Date:  1997-02       Impact factor: 3.780

6.  Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.

Authors:  C Chiang; Y Litingtung; E Lee; K E Young; J L Corden; H Westphal; P A Beachy
Journal:  Nature       Date:  1996-10-03       Impact factor: 49.962

7.  Six3 functions in anterior neural plate specification by promoting cell proliferation and inhibiting Bmp4 expression.

Authors:  Gaia Gestri; Matthias Carl; Irene Appolloni; Stephen W Wilson; Giuseppina Barsacchi; Massimiliano Andreazzoli
Journal:  Development       Date:  2005-04-20       Impact factor: 6.868

8.  Loss of Nkx2.1 homeobox gene function results in a ventral to dorsal molecular respecification within the basal telencephalon: evidence for a transformation of the pallidum into the striatum.

Authors:  L Sussel; O Marin; S Kimura; J L Rubenstein
Journal:  Development       Date:  1999-08       Impact factor: 6.868

9.  Inductive interactions direct early regionalization of the mouse forebrain.

Authors:  K Shimamura; J L Rubenstein
Journal:  Development       Date:  1997-07       Impact factor: 6.868

10.  Overexpression of the forebrain-specific homeobox gene six3 induces rostral forebrain enlargement in zebrafish.

Authors:  M Kobayashi; R Toyama; H Takeda; I B Dawid; K Kawakami
Journal:  Development       Date:  1998-08       Impact factor: 6.868

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  81 in total

1.  Six3 is required for ependymal cell maturation.

Authors:  Alfonso Lavado; Guillermo Oliver
Journal:  Development       Date:  2011-11-09       Impact factor: 6.868

2.  The nuclear hormone receptor Coup-TFII is required for the initiation and early maintenance of Prox1 expression in lymphatic endothelial cells.

Authors:  R Sathish Srinivasan; Xin Geng; Ying Yang; Yingdi Wang; Suraj Mukatira; Michèle Studer; Marianna P R Porto; Oleg Lagutin; Guillermo Oliver
Journal:  Genes Dev       Date:  2010-04-01       Impact factor: 11.361

Review 3.  POMC Neurons: From Birth to Death.

Authors:  Chitoku Toda; Anna Santoro; Jung Dae Kim; Sabrina Diano
Journal:  Annu Rev Physiol       Date:  2017-02-10       Impact factor: 19.318

Review 4.  Cis-regulatory mutations in human disease.

Authors:  Douglas J Epstein
Journal:  Brief Funct Genomic Proteomic       Date:  2009-07-29

5.  Simple and efficient CRISPR/Cas9-mediated targeted mutagenesis in Xenopus tropicalis.

Authors:  Takuya Nakayama; Margaret B Fish; Marilyn Fisher; Jamina Oomen-Hajagos; Gerald H Thomsen; Robert M Grainger
Journal:  Genesis       Date:  2013-12       Impact factor: 2.487

6.  New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Authors:  Sandra Mercier; Christèle Dubourg; Nicolas Garcelon; Boris Campillo-Gimenez; Isabelle Gicquel; Marion Belleguic; Leslie Ratié; Laurent Pasquier; Philippe Loget; Claude Bendavid; Sylvie Jaillard; Lucie Rochard; Chloé Quélin; Valérie Dupé; Véronique David; Sylvie Odent
Journal:  J Med Genet       Date:  2011-09-22       Impact factor: 6.318

7.  The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.

Authors:  Erich Roessler; Kenia B El-Jaick; Christèle Dubourg; Jorge I Vélez; Benjamin D Solomon; Daniel E Pineda-Alvarez; Felicitas Lacbawan; Nan Zhou; Maia Ouspenskaia; Aimée Paulussen; Hubert J Smeets; Ute Hehr; Claude Bendavid; Sherri Bale; Sylvie Odent; Véronique David; Maximilian Muenke
Journal:  Hum Mutat       Date:  2009-10       Impact factor: 4.878

8.  Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.

Authors:  Wei Zhang; Mingi Hong; Gyu-un Bae; Jong-Sun Kang; Robert S Krauss
Journal:  Dis Model Mech       Date:  2010-12-23       Impact factor: 5.758

Review 9.  Eye development and retinogenesis.

Authors:  Whitney Heavner; Larysa Pevny
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-12-01       Impact factor: 10.005

10.  A novel SIX3 mutation segregates with holoprosencephaly in a large family.

Authors:  Benjamin D Solomon; Felicitas Lacbawan; Mahim Jain; Sabina Domené; Erich Roessler; Cynthia Moore; William B Dobyns; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2009-05       Impact factor: 2.802

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