Literature DB >> 10471713

Soma-to-germline interactions during Drosophila oogenesis are influenced by dose-sensitive interactions between cut and the genes cappuccino, ovarian tumor and agnostic.

S M Jackson1, C A Berg.   

Abstract

The cut gene of Drosophila melanogaster encodes a homeodomain protein that regulates a soma-to-germline signaling pathway required for proper morphology of germline cells during oogenesis. cut is required solely in somatic follicle cells, and when cut function is disrupted, membranes separating adjacent nurse cells break down and the structural integrity of the actin cytoskeleton is compromised. To understand the mechanism by which cut expression influences germline cell morphology, we determined whether binucleate cells form by defective cytokinesis or by fusion of adjacent cells. Egg chambers produced by cut, cappuccino, and chickadee mutants contained binucleate cells in which ring canal remnants stained with antibodies against Hu-li tai shao and Kelch, two proteins that are added to ring canals after cytokinesis is complete. In addition, defects in egg chamber morphology were observed only in middle to late stages of oogenesis, suggesting that germline cell cytokineses were normal in these mutants. cut exhibited dose-sensitive genetic interactions with cappuccino but not with chickadee or other genes that regulate cytoskeletal function, including armadillo, spaghetti squash, quail, spire, Src64B, and Tec29A. Genomic regions containing genes that cooperate with cut were identified by performing a second-site noncomplementing screen using a collection of chromosomal deficiencies. Sixteen regions that interact with cut during oogenesis and eight regions that interact during the development of other tissues were identified. Genetic interactions between cut and the ovarian tumor gene were identified as a result of the screen. In addition, the gene agnostic was found to be required during oogenesis, and genetic interactions between cut and agnostic were revealed. These results demonstrate that a signaling pathway regulating the morphology of germline cells is sensitive to genetic doses of cut and the genes cappuccino, ovarian tumor, and agnostic. Since these genes regulate cytoskeletal function and cAMP metabolism, the cut-mediated pathway functionally links these elements to preserve the cytoarchitecture of the germline cells.

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Year:  1999        PMID: 10471713      PMCID: PMC1460760     

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


  50 in total

1.  The villin-like protein encoded by the Drosophila quail gene is required for actin bundle assembly during oogenesis.

Authors:  S Mahajan-Miklos; L Cooley
Journal:  Cell       Date:  1994-07-29       Impact factor: 41.582

2.  Dictyostelium amoebae that lack G-actin-sequestering profilins show defects in F-actin content, cytokinesis, and development.

Authors:  M Haugwitz; A A Noegel; J Karakesisoglou; M Schleicher
Journal:  Cell       Date:  1994-10-21       Impact factor: 41.582

3.  Genetic investigation of cAMP-dependent protein kinase function in Drosophila development.

Authors:  M E Lane; D Kalderon
Journal:  Genes Dev       Date:  1993-07       Impact factor: 11.361

4.  Localization and functions of protein kinase A during Drosophila oogenesis.

Authors:  M E Lane; D Kalderon
Journal:  Mech Dev       Date:  1995-02       Impact factor: 1.882

5.  SRC64 regulates the localization of a Tec-family kinase required for Drosophila ring canal growth.

Authors:  D J Guarnieri; G S Dodson; M A Simon
Journal:  Mol Cell       Date:  1998-05       Impact factor: 17.970

6.  Morphogenesis of Drosophila ovarian ring canals.

Authors:  D N Robinson; K Cant; L Cooley
Journal:  Development       Date:  1994-07       Impact factor: 6.868

7.  Postembryonic patterns of expression of cut, a locus regulating sensory organ identity in Drosophila.

Authors:  K Blochlinger; L Y Jan; Y N Jan
Journal:  Development       Date:  1993-02       Impact factor: 6.868

8.  Diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene.

Authors:  D H Castrillon; S A Wasserman
Journal:  Development       Date:  1994-12       Impact factor: 6.868

9.  A role for the Drosophila segment polarity gene armadillo in cell adhesion and cytoskeletal integrity during oogenesis.

Authors:  M Peifer; S Orsulic; D Sweeton; E Wieschaus
Journal:  Development       Date:  1993-08       Impact factor: 6.868

10.  The Schizosaccharomyces pombe cdc3+ gene encodes a profilin essential for cytokinesis.

Authors:  M K Balasubramanian; B R Hirani; J D Burke; K L Gould
Journal:  J Cell Biol       Date:  1994-06       Impact factor: 10.539

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  5 in total

1.  Identification of genetic loci that interact with cut during Drosophila wing-margin development.

Authors:  Joshua J Krupp; Lauren E Yaich; Robert J Wessells; Rolf Bodmer
Journal:  Genetics       Date:  2005-06-14       Impact factor: 4.562

2.  Identification of new X-chromosomal genes required for Drosophila oogenesis and novel roles for fs(1)Yb, brainiac and dunce.

Authors:  A Swan; S Hijal; A Hilfiker; B Suter
Journal:  Genome Res       Date:  2001-01       Impact factor: 9.043

Review 3.  Subcellular Specialization and Organelle Behavior in Germ Cells.

Authors:  Yukiko M Yamashita
Journal:  Genetics       Date:  2018-01       Impact factor: 4.562

Review 4.  Formins in development: orchestrating body plan origami.

Authors:  Raymond Liu; Elena V Linardopoulou; Gregory E Osborn; Susan M Parkhurst
Journal:  Biochim Biophys Acta       Date:  2008-10-14

5.  A Drosophila homolog of the polyglutamine disease gene SCA2 is a dosage-sensitive regulator of actin filament formation.

Authors:  Terrence F Satterfield; Stephen M Jackson; Leo J Pallanck
Journal:  Genetics       Date:  2002-12       Impact factor: 4.562

  5 in total

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