Literature DB >> 1427039

The Enhancer of split complex and adjacent genes in the 96F region of Drosophila melanogaster are required for segregation of neural and epidermal progenitor cells.

H Schrons1, E Knust, J A Campos-Ortega.   

Abstract

The Enhancer of split complex [E(spl)-C] of Drosophila melanogaster is located in the 96F region of the third chromosome and comprises at least seven structurally related genes, HLH-m delta, HLH-m gamma, HLH-m beta, HLH-m3, HLH-m5, HLH-m7 and E(spl). The functions of these genes are required during early neurogenesis to give neuroectodermal cells access to the epidermal pathway of development. Another gene in the 96F region, namely groucho, is also required for this process. However, groucho is not structurally related to, and appears to act independently of, the genes of the E(spl)-C; the possibility is discussed that groucho acts upstream to the E(spl)-C genes. Indirect evidence suggests that a neighboring transcription unit (m4) may also take part in the process. Of all these genes, only gro is essential; m4 is a dispensable gene, the deletion of which does not produce detectable morphogenetic abnormalities, and the genes of the E(spl)-C are to some extent redundant and can partially substitute for each other. This redundancy is probably due to the fact that the seven genes of the E(spl)-C encode highly conserved putative DNA-binding proteins of the bHLH family. The genes of the complex are interspersed among other genes which appear to be unrelated to the neuroepidermal lineage dichotomy.

Entities:  

Mesh:

Year:  1992        PMID: 1427039      PMCID: PMC1205151     

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


  33 in total

1.  The achaete-scute gene complex of D. melanogaster: conserved domains in a subset of genes required for neurogenesis and their homology to myc.

Authors:  R Villares; C V Cabrera
Journal:  Cell       Date:  1987-07-31       Impact factor: 41.582

2.  Hybrid dysgenesis-induced revertants of insertions at the 5' end of the rudimentary gene in Drosophila melanogaster: transposon-induced control mutations.

Authors:  S Tsubota; P Schedl
Journal:  Genetics       Date:  1986-09       Impact factor: 4.562

3.  The role of easter, an apparent serine protease, in organizing the dorsal-ventral pattern of the Drosophila embryo.

Authors:  R Chasan; K V Anderson
Journal:  Cell       Date:  1989-02-10       Impact factor: 41.582

4.  The expression of three members of the achaete-scute gene complex correlates with neuroblast segregation in Drosophila.

Authors:  C V Cabrera; A Martinez-Arias; M Bate
Journal:  Cell       Date:  1987-07-31       Impact factor: 41.582

5.  A deduced gene product from the Drosophila neurogenic locus, enhancer of split, shows homology to mammalian G-protein beta subunit.

Authors:  D A Hartley; A Preiss; S Artavanis-Tsakonas
Journal:  Cell       Date:  1988-12-02       Impact factor: 41.582

6.  Molecular genetics of the achaete-scute gene complex of D. melanogaster.

Authors:  S Campuzano; L Carramolino; C V Cabrera; M Ruíz-Gómez; R Villares; A Boronat; J Modolell
Journal:  Cell       Date:  1985-02       Impact factor: 41.582

7.  The expression of neurogenic loci in imaginal epidermal cells of Drosophila melanogaster.

Authors:  U Dietrich; J A Campos-Ortega
Journal:  J Neurogenet       Date:  1984-12       Impact factor: 1.250

8.  The white gene as a marker in a new P-element vector for gene transfer in Drosophila.

Authors:  R Klemenz; U Weber; W J Gehring
Journal:  Nucleic Acids Res       Date:  1987-05-26       Impact factor: 16.971

9.  Isolation and characterization of dominant female sterile mutations of Drosophila melanogaster. I. Mutations on the third chromosome.

Authors:  M Erdélyi; J Szabad
Journal:  Genetics       Date:  1989-05       Impact factor: 4.562

10.  The achaete-scute complex is expressed in neurogenic regions of Drosophila embryos.

Authors:  S Romani; S Campuzano; J Modolell
Journal:  EMBO J       Date:  1987-07       Impact factor: 11.598

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  47 in total

1.  Notch signaling directly controls cell proliferation in the Drosophila wing disc.

Authors:  A Baonza; A Garcia-Bellido
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-14       Impact factor: 11.205

2.  Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis.

Authors:  H López-Schier; D St Johnston
Journal:  Genes Dev       Date:  2001-06-01       Impact factor: 11.361

3.  Epigenetic mechanisms of Groucho/Grg/TLE mediated transcriptional repression.

Authors:  Sanjeevkumar R Patel; Samina S Bhumbra; Raghavendra S Paknikar; Gregory R Dressler
Journal:  Mol Cell       Date:  2011-12-08       Impact factor: 17.970

4.  A deficiency screen for zygotic loci required for establishment and patterning of the epidermis in Caenorhabditis elegans.

Authors:  R M Terns; P Kroll-Conner; J Zhu; S Chung; J H Rothman
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

5.  Senseless acts as a binary switch during sensory organ precursor selection.

Authors:  Hamed Jafar-Nejad; Melih Acar; Riitta Nolo; Haluk Lacin; Hongling Pan; Susan M Parkhurst; Hugo J Bellen
Journal:  Genes Dev       Date:  2003-12-01       Impact factor: 11.361

6.  A genome-wide transgenic resource for conditional expression of Drosophila microRNAs.

Authors:  Fernando Bejarano; Diane Bortolamiol-Becet; Qi Dai; Kailiang Sun; Abil Saj; Yu-Ting Chou; David R Raleigh; Kevin Kim; Jian-Quan Ni; Hong Duan; Jr-Shiuan Yang; Tudor A Fulga; David Van Vactor; Norbert Perrimon; Eric C Lai
Journal:  Development       Date:  2012-06-28       Impact factor: 6.868

7.  A novel interaction between hedgehog and Notch promotes proliferation at the anterior-posterior organizer of the Drosophila wing.

Authors:  David J Casso; Brian Biehs; Thomas B Kornberg
Journal:  Genetics       Date:  2010-11-23       Impact factor: 4.562

Review 8.  Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases.

Authors:  Jose L Salazar; Shinya Yamamoto
Journal:  Adv Exp Med Biol       Date:  2018       Impact factor: 2.622

9.  The genetic and molecular organization of the Dopa decarboxylase gene cluster of Drosophila melanogaster.

Authors:  D G Stathakis; E S Pentz; M E Freeman; J Kullman; G R Hankins; N J Pearlson; T R Wright
Journal:  Genetics       Date:  1995-10       Impact factor: 4.562

10.  The WRPW motif of the hairy-related basic helix-loop-helix repressor proteins acts as a 4-amino-acid transcription repression and protein-protein interaction domain.

Authors:  A L Fisher; S Ohsako; M Caudy
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

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