Literature DB >> 6432608

Gene expression during Drosophila melanogaster oogenesis: analysis by in situ hybridization to tissue sections.

L Ambrosio, P Schedl.   

Abstract

The pattern of gene expression for specific genes during oogenesis has been examined by in situ hybridization to RNA in sectioned ovarian preparations. The accumulation (1) of RNA complementary to heat-shock genes, both before and after heat shock; (2) of RNA complementary to three lambda phage recombinants which contain sequences expressed during oogenesis; and (3) of RNA complementary to the rudimentary gene have been analyzed. Gene expression in the ovaries is found to be dependent on both the cell type and the developmental stage of the ovarian chamber. In the nurse cells, the onset of vitellogenesis (stages 8-11) appears to be accompanied by a substantial activation of many different genes and there is a pronounced increase in the level of accumulation of complementary RNAs. Moreover, much of the RNA synthesized in nurse cells during vitellogenesis is ultimately transported into the growing oocyte where it accumulates. It is likely that this accumulation of RNA provides a source of gene products, either as message or proteins, for embryogenesis.

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Year:  1984        PMID: 6432608     DOI: 10.1016/0012-1606(84)90263-x

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  15 in total

1.  Stage-specific localization of the small heat shock protein Hsp27 during oogenesis in Drosophila melanogaster.

Authors:  R Marin; R M Tanguay
Journal:  Chromosoma       Date:  1996-09       Impact factor: 4.316

2.  Polytene chromosomes from ovarian pseudonurse cells of the Drosophila melanogaster otu mutant. I. Photographic map of chromosome 3.

Authors:  T I Heino
Journal:  Chromosoma       Date:  1989-03       Impact factor: 4.316

3.  Multiple functions of Drosophila heat shock transcription factor in vivo.

Authors:  P Jedlicka; M A Mortin; C Wu
Journal:  EMBO J       Date:  1997-05-01       Impact factor: 11.598

4.  Cloning and analysis of fs(1) Ya, a maternal effect gene required for the initiation of Drosophila embryogenesis.

Authors:  H Lin; M F Wolfner
Journal:  Mol Gen Genet       Date:  1989-01

5.  Modifier of rudimentary p1, mod(r)p1, a trans-acting regulatory mutation of rudimentary.

Authors:  D Begley; A M Murphy; C Hiu; S I Tsubota
Journal:  Mol Gen Genet       Date:  1995-07-22

6.  Multiple cis-acting targeting sequences are required for orb mRNA localization during Drosophila oogenesis.

Authors:  V Lantz; P Schedl
Journal:  Mol Cell Biol       Date:  1994-04       Impact factor: 4.272

7.  Organization of transcription units around the Drosophila melanogaster rudimentary locus and temporal pattern of expression.

Authors:  J M Rawls; J N Freund; B P Jarry; C Louis; W A Segraves; P Schedl
Journal:  Mol Gen Genet       Date:  1986-03

8.  A second maternally expressed Drosophila gene encodes a putative RNA helicase of the "DEAD box" family.

Authors:  T de Valoir; M A Tucker; E J Belikoff; L A Camp; C Bolduc; K Beckingham
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-15       Impact factor: 11.205

9.  Enhancer of rudimentaryp1, e(r)p1, a highly conserved enhancer of the rudimentary gene.

Authors:  E Wojcik; A M Murphy; H Fares; K Dang-Vu; S I Tsubota
Journal:  Genetics       Date:  1994-12       Impact factor: 4.562

10.  Molecular cloning and transcript mapping of the dihydroorotate dehydrogenase dhod locus of Drosophila melanogaster.

Authors:  W K Jones; R Kirkpatrick; J M Rawls
Journal:  Mol Gen Genet       Date:  1989-11
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