Expression of Rbp9 during mid-oogenesis induces apoptosis in egg chambers

Kyoungsuk Jeong1, Jeongsil Kim-Ha

  • 1Department of Molecular Biology, School of Natural Sciences, Sejong University, Seoul 143-747, Korea.

Molecules and Cells
|January 28, 2004
PubMed

Insights

Over-expressing the Drosophila RNA binding protein RBP9 causes developmental defects, including apoptosis in egg chambers. Tight control of RBP9 transcription is critical for proper Drosophila development.

Area of Science:

  • Developmental Biology
  • Molecular Biology
  • Genetics

Background:

  • The Drosophila RNA binding protein RBP9 (Rbp9) is expressed in ovarian germline and neuronal cells, specifically in postmitotic cells.
  • Rbp9 is hypothesized to regulate genes involved in cell proliferation and differentiation.

Purpose of the Study:

  • To investigate the effects of ectopic RBP9 expression in Drosophila germline and somatic cells.
  • To understand the role of RBP9 in developmental processes.

Main Methods:

  • Utilized the Gal4 system for ectopic gene expression in Drosophila.
  • Examined developmental defects resulting from RBP9 over-expression in various tissues, particularly during mid-oogenesis.

Main Results:

  • Ectopic RBP9 expression led to severe developmental abnormalities across different tissues.
  • Over-expression during mid-oogenesis induced apoptosis in stage 10 egg chambers, a phenotype similar to Dcp-1 caspase over-expression.
  • The observed phenotype suggests a critical role for RBP9 in regulating cell death pathways during oogenesis.

Conclusions:

  • Tight transcriptional control of RBP9 is essential for normal Drosophila development.
  • RBP9 may function in pathways that prevent inappropriate apoptosis during oogenesis.

Related Concept Videos

Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
Meiosis II01:57

Meiosis II

Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each containing...
Oogenesis02:07

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size reduction of the tissue.
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
Oogenesis01:22

Oogenesis

Oogenesis,  the process of developing egg cells (female gametes), occurs within the ovaries and is fundamental to female fertility. This sequence begins during fetal development when diploid oogonia in the developing ovaries undergo mitotic divisions to produce primary oocytes. By birth, these primary oocytes enter prophase I of meiosis but become arrested in this stage, remaining suspended until puberty.
Each primary oocyte is surrounded by a layer of pre-granulosa cells, forming what is known...