Literature DB >> 28305688

Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : III. Commitment and proliferative capabilities of pole cells and midgut progenitors.

Gerhard M Technau1, Jose A Campos-Ortega1.   

Abstract

In this paper experiments concerning some aspects of the development of pole cells and midgut progenitors in Drosophila are reported. Cells were labelled by injecting horseradish-peroxidase (HRP) in embryos before pole bud formation and transplanted at different stages into unlabelled embryos, where the transplanted cells developed together with the unlabelled cells of the host. The hosts were then fixed and stained at different ages in order to demonstrate the presence of HRP in the progenies of transplanted cells. The main conlusions of the study are as follows. The gonads are the only organ to the formation of which pole cells normally contribute; those pole cells which do not participate in the formation of the gonads are finally eliminated or degenerate. Since the number of primordial germ cells in the gonads is the same irrespective of the number of pole cells present in the embryo, an (unknown) mechanism must exist regulating the final number of pole cells in each of the gonads. After their formation and before reaching the gonads, pole cells have been found to divide only up to two times. With respect to the midgut progenitors, the cells of both anlagen have been found to be committed to develop into midgut, although they behave as equivalent in that they do not apparently distinguish between the anterior and posterior anlage. Midgut progenitors have been found to divide a maximum of three times and to produce two different types of cells, epithelial cells of the midgut wall and spindle-like cells located internally in the gut.

Entities:  

Keywords:  Cell lineages; Drosophila; Embryogenesis; Pole cells and midgut progenitors

Year:  1986        PMID: 28305688     DOI: 10.1007/BF00375889

Source DB:  PubMed          Journal:  Rouxs Arch Dev Biol        ISSN: 0930-035X


  12 in total

1.  Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : II. Commitment and proliferative capabilities of neural and epidermal cell progenitors.

Authors:  Gerhard M Technau; Jose A Campos-Ortega
Journal:  Rouxs Arch Dev Biol       Date:  1986-09

2.  The peripheral nervous system of mutants of early neurogenesis inDrosophila melanogaster.

Authors:  Volker Hartenstein; Jose A Campos-Ortega
Journal:  Rouxs Arch Dev Biol       Date:  1986-05

3.  The potentialities of transplanted early gastrula nuclei ofDrosophila melanogaster. Production of their imago descendants by germ-line transplantation.

Authors:  Karl Illmensee
Journal:  Wilhelm Roux Arch Entwickl Mech Org       Date:  1973-12

Review 4.  Drosophila chimeras and the problem of determination.

Authors:  K Illmensee
Journal:  Results Probl Cell Differ       Date:  1978

Review 5.  The role of cell lineage in development.

Authors:  G S Stent
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1985-12-17       Impact factor: 6.237

6.  The autonomous function of germ plasm in a somatic region of the Drosophila egg.

Authors:  K Illmensee; A P Mahowald
Journal:  Exp Cell Res       Date:  1976-01       Impact factor: 3.905

7.  Developmental fate of pole cells in Drosophila melanogaster.

Authors:  E M Underwood; J H Caulton; C D Allis; A P Mahowald
Journal:  Dev Biol       Date:  1980-06-15       Impact factor: 3.582

8.  Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : I. The method.

Authors:  Gerhard Martin Technau
Journal:  Rouxs Arch Dev Biol       Date:  1986-08

9.  Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis.

Authors:  V E Foe; B M Alberts
Journal:  J Cell Sci       Date:  1983-05       Impact factor: 5.285

10.  Interspecific transplantation of polar plasm between Drosophila embryos.

Authors:  A P Mahowald; K Illmensee; F R Turner
Journal:  J Cell Biol       Date:  1976-08       Impact factor: 10.539

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  9 in total

1.  Nanos suppresses somatic cell fate in Drosophila germ line.

Authors:  Yoshiki Hayashi; Makoto Hayashi; Satoru Kobayashi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-06       Impact factor: 11.205

2.  Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : IV. Commitment and proliferative capabilities of mesodermal cells.

Authors:  Justinus Beer; Gerhard M Technau; Jose A Campos-Ortega
Journal:  Rouxs Arch Dev Biol       Date:  1987-04

3.  Genes controlling posterior gut development in theDrosophila embryo.

Authors:  Ruth Harbecke; Judith A Lengyel
Journal:  Rouxs Arch Dev Biol       Date:  1995-05

4.  Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : II. Commitment and proliferative capabilities of neural and epidermal cell progenitors.

Authors:  Gerhard M Technau; Jose A Campos-Ortega
Journal:  Rouxs Arch Dev Biol       Date:  1986-09

5.  Apvasa marks germ-cell migration in the parthenogenetic pea aphid Acyrthosiphon pisum (Hemiptera: Aphidoidea).

Authors:  Chun-Che Chang; Gee-Way Lin; Charles E Cook; Shwu-Bin Horng; How-Jin Lee; Ting-Yu Huang
Journal:  Dev Genes Evol       Date:  2007-02-27       Impact factor: 0.900

6.  Reversible commitment of neural and epidermal progenitor cells during embryogenesis of Drosophila melanogaster.

Authors:  Gerhard M Technau; Thomas Becker; Jose A Campos-Ortega
Journal:  Rouxs Arch Dev Biol       Date:  1988-12

7.  aproctous, a locus that is necessary for the development of the proctodeum in Drosophila embryos, encodes a homolog of the vertebrate Brachyury gene.

Authors:  Ryutaro Murakami; Ayako Shigenaga; Morikazu Kawakita; Koichi Takimoto; Ikuo Yamaoka; Koji Akasaka; Hiraku Shimada
Journal:  Rouxs Arch Dev Biol       Date:  1995-09

8.  Lineage analysis of transplanted individual cells in embryos of Drosophila melanogaster : I. The method.

Authors:  Gerhard Martin Technau
Journal:  Rouxs Arch Dev Biol       Date:  1986-08

9.  A C. elegans LSD1 demethylase contributes to germline immortality by reprogramming epigenetic memory.

Authors:  David J Katz; T Matthew Edwards; Valerie Reinke; William G Kelly
Journal:  Cell       Date:  2009-04-17       Impact factor: 41.582

  9 in total

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