Page last updated: 2024-10-24

establishment of meiotic spindle localization

Definition

Target type: biologicalprocess

The cell cycle process in which the directed movement of the meiotic spindle to a specific location in the cell occurs. [GOC:ai]

The meiotic spindle, a specialized microtubule structure essential for accurate chromosome segregation during meiosis, undergoes a precise and intricate process of localization. This process is crucial for ensuring proper chromosome alignment and segregation, ultimately leading to the formation of haploid gametes. Here's a detailed breakdown of the biological events involved in establishing meiotic spindle localization:

**1. Nuclear Envelope Breakdown (NEBD):**
- The nuclear envelope, which encloses the genetic material, breaks down during prophase I, allowing the spindle microtubules access to the chromosomes.
- This event is triggered by phosphorylation of lamins, proteins that form the nuclear lamina, by cyclin-dependent kinases (CDKs).

**2. Microtubule Nucleation and Polymerization:**
- Microtubule organizing centers (MTOCs), specifically the centrosomes in most organisms, initiate the assembly of microtubules.
- MTOCs contain γ-tubulin ring complexes (γTuRCs), which serve as nucleation sites for microtubule polymerization.
- The microtubules elongate by the addition of tubulin subunits, forming a network within the cytoplasm.

**3. Spindle Pole Formation:**
- MTOCs, positioned at opposite poles of the cell, become the spindle poles.
- As microtubules emanate from the poles, they interact with each other and with the chromosomes, leading to the formation of the bipolar spindle structure.

**4. Chromosome Attachment:**
- The kinetochores, protein complexes assembled at centromeres of chromosomes, serve as attachment sites for spindle microtubules.
- Kinetochore microtubules (K-fibers) attach to kinetochores, creating a physical link between chromosomes and the spindle poles.
- The attachment is highly regulated, ensuring that each chromosome is attached to microtubules emanating from opposite poles.

**5. Spindle Pole Positioning:**
- Spindle poles are not stationary; they undergo movements to achieve proper spindle orientation and localization.
- Factors influencing spindle pole positioning include:
- **Cortical cues:** Proteins embedded in the cell cortex (the outer layer of the cytoplasm) can guide spindle pole movements.
- **Astral microtubules:** Microtubules extending from the spindle poles interact with the cell cortex, influencing pole positioning.
- **Microtubule motors:** Motor proteins, such as dynein and kinesin, contribute to spindle pole movements by interacting with microtubules and the cell cortex.

**6. Spindle Assembly Checkpoint (SAC):**
- The SAC ensures that all chromosomes are correctly attached to the spindle before proceeding to anaphase.
- It monitors kinetochore-microtubule attachments and delays anaphase onset until all chromosomes are properly aligned.

**7. Spindle Elongation and Anaphase Separation:**
- Once all chromosomes are properly attached and aligned, the SAC is satisfied, and the cell progresses to anaphase.
- During anaphase, the spindle elongates, and the sister chromatids of each chromosome are pulled apart toward opposite poles by the shortening of kinetochore microtubules.
- This separation ensures that each daughter cell receives a complete set of chromosomes.

**8. Cytokinesis:**
- Following chromosome segregation, cytokinesis, the division of the cytoplasm, occurs.
- This process forms two daughter cells, each with a complete set of chromosomes and its own nucleus.

The establishment of meiotic spindle localization is a dynamic process that involves a complex interplay of molecular events and structural components. It is crucial for ensuring accurate chromosome segregation during meiosis, thereby contributing to genetic diversity and the production of functional gametes.'
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Proteins (1)

ProteinDefinitionTaxonomy
Myosin-9A myosin-9 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P35579]Homo sapiens (human)

Compounds (1)

CompoundDefinitionClassesRoles
blisterblebbistatin : A pyrroloquinoline that is 1,2,3,3a-tetrahydro-H-pyrrolo[2,3-b]quinolin-4-one substituted by a hydroxy group at position 3a, a methyl group at position 6 and a phenyl group at position 1. It acts as an inhibitor of ATPase activity of non-muscle myosin II.

blebbistatin: structure in first source
cyclic ketone;
pyrroloquinoline;
tertiary alcohol;
tertiary alpha-hydroxy ketone
inhibitor