Literature DB >> 10835393

Molecular analysis of Drosophila eyes absent mutants reveals features of the conserved Eya domain.

Q T Bui1, J E Zimmerman, H Liu, N M Bonini.   

Abstract

The eyes absent (eya) gene is critical to eye formation in Drosophila; upon loss of eya function, eye progenitor cells die by programmed cell death. Moreover, ectopic eya expression directs eye formation, and eya functionally synergizes in vivo and physically interacts in vitro with two other genes of eye development, sine oculis and dachshund. The Eya protein sequence, while highly conserved to vertebrates, is novel. To define amino acids critical to the function of the Eya protein, we have sequenced eya alleles. These mutations have revealed that loss of the entire Eya Domain is null for eya activity, but that alleles with truncations within the Eya Domain display partial function. We then extended the molecular genetic analysis to interactions within the Eya Domain. This analysis has revealed regions of special importance to interaction with Sine Oculis or Dachshund. Select eya missense mutations within the Eya Domain diminished the interactions with Sine Oculis or Dachshund. Taken together, these data suggest that the conserved Eya Domain is critical for eya activity and may have functional subregions within it.

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Year:  2000        PMID: 10835393      PMCID: PMC1461105     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  30 in total

1.  Cloning and characterization of two vertebrate homologs of the Drosophila eyes absent gene.

Authors:  J E Zimmerman; Q T Bui; E Steingrímsson; D L Nagle; W Fu; A Genin; N B Spinner; N G Copeland; N A Jenkins; M Bucan; N M Bonini
Journal:  Genome Res       Date:  1997-02       Impact factor: 9.043

2.  Eyes absent: a gene family found in several metazoan phyla.

Authors:  M K Duncan; L Kos; N A Jenkins; D J Gilbert; N G Copeland; S I Tomarev
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

3.  sine oculis is a homeobox gene required for Drosophila visual system development.

Authors:  M A Serikaku; J E O'Tousa
Journal:  Genetics       Date:  1994-12       Impact factor: 4.562

4.  Six class homeobox genes in drosophila belong to three distinct families and are involved in head development.

Authors:  H C Seo; J Curtiss; M Mlodzik; A Fjose
Journal:  Mech Dev       Date:  1999-05       Impact factor: 1.882

5.  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

Review 6.  A fly's eye view of biology.

Authors:  B J Thomas; D A Wassarman
Journal:  Trends Genet       Date:  1999-05       Impact factor: 11.639

7.  Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.

Authors:  P X Xu; J Adams; H Peters; M C Brown; S Heaney; R Maas
Journal:  Nat Genet       Date:  1999-09       Impact factor: 38.330

8.  Ectopic eye development in Drosophila induced by directed dachshund expression.

Authors:  W Shen; G Mardon
Journal:  Development       Date:  1997-01       Impact factor: 6.868

9.  Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode.

Authors:  P X Xu; I Woo; H Her; D R Beier; R L Maas
Journal:  Development       Date:  1997-01       Impact factor: 6.868

10.  Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development.

Authors:  G Oliver; A Mailhos; R Wehr; N G Copeland; N A Jenkins; P Gruss
Journal:  Development       Date:  1995-12       Impact factor: 6.868

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  23 in total

1.  Functional dissection of eyes absent reveals new modes of regulation within the retinal determination gene network.

Authors:  Serena J Silver; Erin L Davies; Laura Doyon; Ilaria Rebay
Journal:  Mol Cell Biol       Date:  2003-09       Impact factor: 4.272

Review 2.  The Eyes Absent proteins in development and disease.

Authors:  Emmanuel Tadjuidje; Rashmi S Hegde
Journal:  Cell Mol Life Sci       Date:  2012-09-13       Impact factor: 9.261

3.  Pleiotropy in Drosophila organogenesis: Mechanistic insights from Combgap and the retinal determination gene network.

Authors:  Trevor L Davis; Ilaria Rebay
Journal:  Fly (Austin)       Date:  2017-12-12       Impact factor: 2.160

4.  Using Drosophila to decipher how mutations associated with human branchio-oto-renal syndrome and optical defects compromise the protein tyrosine phosphatase and transcriptional functions of eyes absent.

Authors:  Mousumi Mutsuddi; Benjamin Chaffee; Justin Cassidy; Serena J Silver; Tina L Tootle; Ilaria Rebay
Journal:  Genetics       Date:  2005-03-31       Impact factor: 4.562

5.  The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear.

Authors:  Olivier Bricaud; Andres Collazo
Journal:  J Neurosci       Date:  2006-10-11       Impact factor: 6.167

6.  Identification of transcriptional targets of the dual-function transcription factor/phosphatase eyes absent.

Authors:  Jennifer Jemc; Ilaria Rebay
Journal:  Dev Biol       Date:  2007-07-27       Impact factor: 3.582

7.  The retinal determination gene eyes absent is regulated by the EGF receptor pathway throughout development in Drosophila.

Authors:  Claire L Salzer; Yair Elias; Justin P Kumar
Journal:  Genetics       Date:  2009-11-02       Impact factor: 4.562

8.  Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations.

Authors:  Aaron N Patrick; Barbara J Schiemann; Kui Yang; Rui Zhao; Heide L Ford
Journal:  J Biol Chem       Date:  2009-06-04       Impact factor: 5.157

9.  Drosophila mutants show NMD pathway activity is reduced, but not eliminated, in the absence of Smg6.

Authors:  Kimberly A Frizzell; Shawn G Rynearson; Mark M Metzstein
Journal:  RNA       Date:  2012-06-27       Impact factor: 4.942

10.  EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis.

Authors:  Youe Li; Jose M Manaligod; Daniel L Weeks
Journal:  Biol Cell       Date:  2010-02-17       Impact factor: 4.458

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