The mechanisms of MTOCs maturation in human and mouse oocytes

Hao Gu1, Ling Wu2, Mingru Yin2

  • 1Institute of Pediatrics, Children's Hospital of Fudan University, State Key Laboratory of Genetic Engineering, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.

Science Bulletin
|September 3, 2025
PubMed

Insights

Microtubule organizing centers (MTOCs) in oocytes mature through activation and migration, a conserved process involving CKAP5 and TACC3. Impaired maturation links to aging and spindle failure.

Area of Science:

  • Cell Biology
  • Reproductive Biology
  • Oocyte Development

Background:

  • Microtubule organizing centers (MTOCs) are crucial for meiotic spindle assembly and chromosome segregation in oocytes.
  • Previous research primarily examined MTOCs in metaphase I, leaving dynamics in germinal vesicle (GV) oocytes understudied.

Purpose of the Study:

  • To investigate the dynamic changes and underlying mechanisms of MTOC maturation in human and mouse GV oocytes.
  • To elucidate the roles of specific proteins in MTOC maturation and its implications for oocyte quality.

Main Methods:

  • Exploration of MTOC dynamics in human and mouse GV oocytes.
  • Investigation of the involvement of cytoskeleton-associated protein 5 (CKAP5) and transforming acidic coiled-coil containing protein 3 (TACC3).
  • Analysis of the roles of dynein/dynactin in MTOC migration.

Main Results:

  • MTOC maturation is a conserved process in GV oocytes, involving activation and migration.
  • CKAP5 and TACC3 are key players in oocyte MTOC maturation.
  • MTOC activation precedes migration, which is facilitated by dynein/dynactin.
  • Disruption of MTOC maturation leads to spindle assembly failure.
  • Impaired MTOC maturation is associated with oocyte aging.

Conclusions:

  • MTOC maturation in GV oocytes is a conserved, two-step process essential for reproductive success.
  • CKAP5, TACC3, and dynein/dynactin are critical for MTOC dynamics and oocyte quality.
  • Understanding MTOC maturation provides insights into oocyte aging and potential fertility issues.

Related Concept Videos

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...
64.3K
Meiosis II02:02

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,...
46.3K
Meiosis vs. Mitosis02:57

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...
58.1K
Folliculogenesis01:20

Folliculogenesis

Folliculogenesis is the development of ovarian follicles, the specialized structures within the ovarian cortex where oogenesis, or egg development, occurs. This process is essential for female reproductive health and begins during fetal development when primordial follicles are formed. Each primordial follicle comprises a primary oocyte in the center, surrounded by a single layer of squamous pre-granulosa cells. These follicles remain dormant in late prophase I of meiosis until triggered by...
1.1K
M-Cdk Drives Transition Into Mitosis02:15

M-Cdk Drives Transition Into Mitosis

Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
5.7K
Microtubule Formation01:23

Microtubule Formation

Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation...
5.9K