Induction of indora expression in pole cells by the mesoderm is required for female germ-line development in Drosophila melanogaster

Development ◽  
1999 ◽  
Vol 126 (5) ◽  
pp. 1023-1029 ◽  
Author(s):  
M. Mukai ◽  
M. Kashikawa ◽  
S. Kobayashi
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Cells ◽  
Germ Line ◽  
Animal Groups ◽  
Novel Transcript ◽  
Expression Of Genes ◽  
Female Germ Line ◽  
Pole Cells

In many animal groups, the interaction between germ and somatic line is required for germ-line development. In Drosophila, the germ-line precursors (pole cells) formed at the posterior tip of the embryos migrate toward the mesodermal layer where they adhere to the dorsolateral mesoderm, which ensheaths the pole cells to form the embryonic gonads. These mesodermal cells may control the expression of genes that function in pole cells for their development into germ cells. However, such downstream genes have not been isolated. In this study, we identify a novel transcript, indora (idr), which is expressed only in pole cells within the gonads. Reduction of idr transcripts by an antisense idr expression caused the failure of pole cells to produce functional germ cells in females. Furthermore, we demonstrate that idr expression depends on the presence of the dorsolateral mesoderm, but it does not necessarily require its specification as the gonadal mesoderm. Our findings suggest that the induction of idr in pole cells by the mesodermal cells is required for germ-line development.

Multiple products from the shavenbaby-ovo gene region of Drosophila melanogaster: relationship to genetic complexity

1994 ◽  
Vol 14 (10) ◽  
pp. 6809-6818
Author(s):  
M D Garfinkel ◽  
J Wang ◽  
Y Liang ◽  
A P Mahowald
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Line ◽  
Gene Region ◽  
Multiple Products ◽  
Zinc Finger Motifs ◽  
Genetic Complexity ◽  
Complex Locus ◽  
Female Germ Line ◽  
Sensory Structures ◽  
Pole Cells

The Drosophila melanogaster shavenbaby (svb)-ovo gene region is a complex locus, containing two distinct but comutable genetic functions. ovo is required for survival and differentiation of female germ line cells and plays a role in germ line sex determination. In contrast, svb is required in both male and female embryos for the production of epidermal locomotor and sensory structures. Sequences required for the two genetic functions are partially overlapping. ovo corresponds to a previously described germ line-dependent 5.0-kb poly(A)+ mRNA that first appears in the germarium and accumulates in nurse cells during oogenesis. The 5.0-kb mRNA is stored in the egg, but it is rapidly lost in the embryos except for its continued presence in the germ line precursor pole cells. The ovo mRNA predicts a 1,028-amino-acid 110.6-kDa protein homologous with transcription factors. We have identified an embryonic mRNA, 7.1 kb in length, that contains exons partially overlapping those of the 5.0-kb poly(A)+ mRNA. The spatial distribution of this newly discovered transcript during midembryogenesis suggests that it corresponds to the svb function. The arrangement of exons common to the 5.0- and 7.1-kb mRNAs suggests that the Ovo and Svb proteins share DNA-binding specificity conferred by four Cys2-His2 zinc finger motifs but differ functionally in their capacity to interact with other components of the transcription machinery.

scholarly journals Multiple products from the shavenbaby-ovo gene region of Drosophila melanogaster: relationship to genetic complexity.

1994 ◽  
Vol 14 (10) ◽  
pp. 6809-6818 ◽  
Author(s):  
M D Garfinkel ◽  
J Wang ◽  
Y Liang ◽  
A P Mahowald
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Line ◽  
Gene Region ◽  
Multiple Products ◽  
Zinc Finger Motifs ◽  
Genetic Complexity ◽  
Complex Locus ◽  
Female Germ Line ◽  
Sensory Structures ◽  
Pole Cells

The Drosophila melanogaster shavenbaby (svb)-ovo gene region is a complex locus, containing two distinct but comutable genetic functions. ovo is required for survival and differentiation of female germ line cells and plays a role in germ line sex determination. In contrast, svb is required in both male and female embryos for the production of epidermal locomotor and sensory structures. Sequences required for the two genetic functions are partially overlapping. ovo corresponds to a previously described germ line-dependent 5.0-kb poly(A)+ mRNA that first appears in the germarium and accumulates in nurse cells during oogenesis. The 5.0-kb mRNA is stored in the egg, but it is rapidly lost in the embryos except for its continued presence in the germ line precursor pole cells. The ovo mRNA predicts a 1,028-amino-acid 110.6-kDa protein homologous with transcription factors. We have identified an embryonic mRNA, 7.1 kb in length, that contains exons partially overlapping those of the 5.0-kb poly(A)+ mRNA. The spatial distribution of this newly discovered transcript during midembryogenesis suggests that it corresponds to the svb function. The arrangement of exons common to the 5.0- and 7.1-kb mRNAs suggests that the Ovo and Svb proteins share DNA-binding specificity conferred by four Cys2-His2 zinc finger motifs but differ functionally in their capacity to interact with other components of the transcription machinery.

Genetic control of sex determination in the germ line and soma of the housefly, Musca domestica

Development ◽  
1994 ◽  
Vol 120 (9) ◽  
pp. 2531-2538 ◽  
Author(s):  
D. Hilfiker-Kleiner ◽  
A. Dubendorfer ◽  
A. Hilfiker ◽  
R. Nothiger
Keyword(s):  
Sex Determination ◽  
Musca Domestica ◽  
Germ Cells ◽  
Maternal Effect ◽  
Germ Line ◽  
M Cells ◽  
Female Genotype ◽  
Female Germ Line ◽  
Pole Cells

In Musca domestica, sex in the soma is cell autonomously determined by the male-determiner M, or by the female-determiner FD. Transplanted pole cells (precursors of the germ line) show that sex determination of germ cells is non-autonomous genotypically male pole cells form functional eggs in female hosts, and genotypically female pole cells form functional sperm in male hosts. When M/+ cells undergo oogenesis, a male-determining maternal effect predetermines offspring without M, i.e. of female genotype, to develop as fertile males. FD is epistatic to M in the female germ line, as it is in the soma, overruling the masculinizing effect of M. The results suggest that maternal F product is needed for activation of the zygotic F gene.

Sex determination in the germ line of Drosophila melanogaster: activation of the gene Sex-lethal

Development ◽  
1993 ◽  
Vol 118 (3) ◽  
pp. 813-816 ◽  
Author(s):  
B. Granadino ◽  
P. Santamaria ◽  
L. Sanchez
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Cells ◽  
Germ Line ◽  
Wild Type ◽  
Female Development ◽  
Pole Cell ◽  
Somatic Tissues ◽  
Wild Type Female ◽  
Sex Lethal ◽  
Pole Cell Transplantation

The germ line exhibits sexual dimorphism as do the somatic tissues. Cells with the 2X;2A chromosome constitution will follow the oogenic pathway and X;2A cells will develop into sperm. In both somatic and germ-line tissues, the sexual pathway chosen by the cells depends on the gene Sex-lethal (Sxl), whose function is continuously needed for female development. In the soma, the sex of the cells is autonomously determined by the X:A signal while, in the germ line, the sex is determined by cell autonomous (the X:A signal) and somatic inductive signals. Three X-linked genes have been identified, scute (sc), sisterless-a (sis-a) and runt (run), that determine the initial functional state of Sxl in the soma. Using pole cell transplantation, we have tested whether these genes are also needed to activate Sxl in the germ line. We found that germ cells simultaneously heterozygous for sc, sis-a, run and a deficiency for Sxl transplanted into wild-type female hosts develop into functional oocytes. We conclude that the genes sc, sis-a and run needed to activate Sxl in the soma seem not to be required to activate this gene in the germ line; therefore, the X:A signal would be made up by different genes in somatic and germ-line tissues. The Sxlf7M1/Sxlfc females do not have developed ovaries. We have shown that germ cells of this genotype transplanted into wild-type female hosts produce functional oocytes. We conclude that the somatic component of the gonads in Sxlf7M1/Sxlfc females is affected, and consequently germ cells do not develop.(ABSTRACT TRUNCATED AT 250 WORDS)

Identification of genes expressed in human primordial germ cells at the time of entry of the female germ line into meiosis

1999 ◽  
Vol 5 (9) ◽  
pp. 851-860 ◽  
Author(s):  
Tetsuya Goto ◽  
James Adjaye ◽  
Charles H. Rodeck ◽  
Marilyn Monk
Keyword(s):  
Germ Cells ◽  
Germ Line ◽  
Primordial Germ Cells ◽  
Female Germ Line

scholarly journals Mitochondrial functionality in female reproduction

2017 ◽  
Vol 71 (1) ◽  
pp. 0-0
Author(s):  
Łukasz Gąsior ◽  
Regina Daszkiewicz ◽  
Mateusz Ogórek ◽  
Zbigniew Polański
Keyword(s):  
Mitochondrial Genome ◽  
Germ Cells ◽  
Germ Line ◽  
Whole Body ◽  
Female Reproduction ◽  
Normal Number ◽  
Female Germ Line ◽  
And Function ◽  
Role And Function

In most animal species female germ cells are the source of mitochondrial genome for the whole body of individuals. As a source of mitochondrial DNA for future generations the mitochondria in the female germ line undergo dynamic quantitative and qualitative changes. In addition to maintaining the intact template of mitochondrial genome from one generation to another, mitochondrial role in oocytes is much more complex and pleiotropic. The quality of mitochondria determines the ability of meiotic divisions, fertilization ability, and activation after fertilization or sustaining development of a new embryo. The presence of normal number of functional mitochondria is also crucial for proper implantation and pregnancy maintaining. This article addresses issues of mitochondrial role and function in mammalian oocyte and presents new approaches in studies of mitochondrial function in female germ cells.

Sign in / Sign up

Export Citation Format

Share Document