Related Experiment Video
Updated: May 24, 2026

09:16
Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
Localization and function of the Ska complex during mouse oocyte meiotic maturation
Qing-Hua Zhang1, Shu-Tao Qi, Zhen-Bo Wang
1State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Cell Cycle (Georgetown, Tex.)
|February 17, 2012
Summary
The spindle and kinetochore-associated (Ska) complex is crucial for mouse oocyte meiosis, regulating spindle movement and stability. Its function differs from mitosis, highlighting its unique role in oocyte maturation.
Area of Science:
- Cell Biology
- Developmental Biology
- Reproductive Biology
Background:
- The spindle and kinetochore-associated (Ska) complex is vital for chromosome segregation during mitosis.
- Its specific functions and localization during meiosis, particularly in oocytes, are not well understood.
Purpose of the Study:
- To investigate the localization and function of the Ska complex during mouse oocyte meiotic maturation.
- To compare the meiotic roles of the Ska complex with its known mitotic functions.
Main Methods:
- Localization studies of Ska complex proteins in mouse oocytes.
- Functional analysis using Morpholino knockdown of Ska complex members.
- Time-lapse live imaging to observe spindle dynamics and polar body extrusion.
- Exogenous Myc-Ska mRNA injection to assess rescue effects.
Main Results:
- Ska complex members localize to spindle microtubules, not kinetochores, during mouse oocyte meiosis (Pro-MI to MII stages).
- Knockdown of Ska complex components causes spindle movement defects and enlarged polar bodies.
- Depletion of the Ska complex impairs anaphase spindle stability and first polar body extrusion.
Conclusions:
- The Ska complex plays essential roles in meiotic spindle migration and anaphase spindle stability during mouse oocyte maturation.
- The localization and function of the Ska complex in meiosis differ significantly from its role in mitosis.
Related Concept Videos
Meiosis II
Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
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...
Meiosis vs. Mitosis
Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
The Spindle Assembly Checkpoint
The spindle assembly checkpoint is a molecular surveillance mechanism ensuring the fidelity of chromosome segregation during anaphase. The checkpoint monitors the completion of all the prerequisite steps before chromosome segregation to determine whether the segregation process should proceed or be delayed.
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
The Mitotic Spindle
The mitotic spindle—or spindle apparatus—is a eukaryotic, cytoskeletal structure made up of long protein fibers called microtubules. Formed during cell division, the spindle separates sister chromatids and moves them to opposite ends of a parental cell, where the now individual chromosomes are distributed to two daughter cell nuclei.
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
The bipolar configuration of the mitotic spindle facilitates chromosomal segregation, preparing the cell for division. One mechanism that ensures bipolar mitotic...
Meiosis I
Meiosis is the division of a diploid cell into haploid cells forming sperm and eggs in animals through differentiation. Meiosis I is the first stage of meiosis, where the genetic recombination of homologous chromosomes and the reduction of the ploidy level by half occurs.
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...

