Literature DB >> 15207846

The role of Zic genes in neural development.

Jun Aruga1.   

Abstract

The Zic family of zinc-finger proteins plays a crucial role in neural development. Zic genes are vertebrate homologs of odd-paired, the Drosophila pair-rule gene. Their gene products have zinc-finger domains similar to those of Gli proteins, which act as transcriptional regulators in hedgehog signaling. Recent studies of human, mouse, frog, fish and ascidian Zic homologs have provided evidence that Zic genes are involved in a variety of developmental processes, including neurogenesis, myogenesis, skeletal patterning, and left-right axis establishment. Zic genes appear to have multiple roles in neural development. They control the initial phase during which ectoderm differentiates into neuroectoderm, and they may act as bridges between secreted neural tissue induction signals and the basic-helix-loop-helix class of neurogenesis-inducing transcriptional regulatory factors. Studies of loss-of-function mutations with differing Zic gene subtypes show that the Zic family of genes controls the process of neurulation. Mutations result in neural tube defects, which are seen at different rostrocaudal levels depending on which Zic gene subtype has been affected. Development of holoprosencephaly, forebrain anomalies, and cerebellar dysgenesis indicate that region-specific morphogenesis of the CNS is also controlled by Zic genes. The underlying molecular actions of Zic gene products, which allow them to control development, remain a mystery. Recent molecular characterization has shown that Zic proteins are able to bind Gli-binding DNA sequences in a sequence-specific manner, but with lower affinity than Gli proteins. Zic proteins also can activate transcription from several promoters. Furthermore, Zic and Gli proteins interact physically via their zinc-finger domains, raising the possibility that Zic proteins can act as transcriptional cofactors and modulate the hedgehog-signaling pathway. Clarification of the specific cooperating factors is therefore required in each case. Other evidence also suggests that Zic proteins can inhibit neuronal differentiation by activating Notch signals. This association might be is a clue toward understanding of the multifunctional property of Zic proteins because Notch signaling also is implicated in the control of several developmental processes. Copyright 2004 Elsevier Inc.

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Year:  2004        PMID: 15207846     DOI: 10.1016/j.mcn.2004.01.004

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  91 in total

1.  CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592.

Authors:  Elsa Nicolas; Yannick Poitelon; Eliane Chouery; Nabiha Salem; Nicolas Levy; André Mégarbané; Valérie Delague
Journal:  Eur J Hum Genet       Date:  2010-06-09       Impact factor: 4.246

2.  An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis.

Authors:  Ashley E Cast; Chunlei Gao; Jeffrey D Amack; Stephanie M Ware
Journal:  Dev Biol       Date:  2012-01-21       Impact factor: 3.582

3.  Zic3 is required for maintenance of pluripotency in embryonic stem cells.

Authors:  Linda Shushan Lim; Yuin-Han Loh; Weiwei Zhang; Yixun Li; Xi Chen; Yinan Wang; Manjiri Bakre; Huck-Hui Ng; Lawrence W Stanton
Journal:  Mol Biol Cell       Date:  2007-01-31       Impact factor: 4.138

4.  Differentiation of ES cells into cerebellar neurons.

Authors:  Enrique Salero; Mary E Hatten
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-09       Impact factor: 11.205

Review 5.  SHH pathway and cerebellar development.

Authors:  Catherine Vaillant; Denis Monard
Journal:  Cerebellum       Date:  2009-02-18       Impact factor: 3.847

6.  Zic2 regulates retinal ganglion cell axon avoidance of ephrinB2 through inducing expression of the guidance receptor EphB1.

Authors:  Ramee Lee; Timothy J Petros; Carol A Mason
Journal:  J Neurosci       Date:  2008-06-04       Impact factor: 6.167

7.  Presenilin-based genetic screens in Drosophila melanogaster identify novel notch pathway modifiers.

Authors:  Matt B Mahoney; Annette L Parks; David A Ruddy; Stanley Y K Tiong; Hanife Esengil; Alexander C Phan; Panos Philandrinos; Christopher G Winter; Runa Chatterjee; Kari Huppert; William W Fisher; Lynn L'Archeveque; Felipa A Mapa; Wendy Woo; Michael C Ellis; Daniel Curtis
Journal:  Genetics       Date:  2006-01-16       Impact factor: 4.562

8.  The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.

Authors:  Erich Roessler; Felicitas Lacbawan; Christèle Dubourg; Aimee Paulussen; Jos Herbergs; Ute Hehr; Claude Bendavid; Nan Zhou; Maia Ouspenskaia; Sherri Bale; Sylvie Odent; Vèronique David; Maximilian Muenke
Journal:  Hum Mutat       Date:  2009-04       Impact factor: 4.878

9.  Expression pattern of annelid Zic in embryonic development of the oligochaete Tubifex tubifex.

Authors:  Hirokazu Takahashi; Takashi Shimizu; Jun Aruga
Journal:  Dev Genes Evol       Date:  2008-09-23       Impact factor: 0.900

10.  Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort.

Authors:  Lucilene A Ribeiro; Erich Roessler; Ping Hu; Daniel E Pineda-Alvarez; Nan Zhou; Marypat Jones; Settara Chandrasekharappa; Antonio Richieri-Costa; Maximilian Muenke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-07-27
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