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The Spindle Assembly Checkpoint02:19

The Spindle Assembly Checkpoint

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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...
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Nuclear Stability03:18

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Protons and neutrons, collectively called nucleons, are packed together tightly in a nucleus. With a radius of about 10−15 meters, a nucleus is quite small compared to the radius of the entire atom, which is about 10−10 meters. Nuclei are extremely dense compared to bulk matter, averaging 1.8 × 1014 grams per cubic centimeter. If the earth’s density were equal to the average nuclear density, the earth’s radius would be only about 200 meters.
To hold positively charged protons together...
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Nuclear Fusion02:45

Nuclear Fusion

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The process of converting very light nuclei into heavier nuclei is also accompanied by the conversion of mass into large amounts of energy, a process called fusion. The principal source of energy in the sun is a net fusion reaction in which four hydrogen nuclei fuse and ultimately produce one helium nucleus and two positrons.
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Non-nuclear Inheritance01:29

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Most DNA resides in the nucleus of a cell. However, some organelles in the cell cytoplasm⁠—such as chloroplasts and mitochondria⁠—also have their own DNA. These organelles replicate their DNA independently of the nuclear DNA of the cell in which they reside. Non-nuclear inheritance describes the inheritance of genes from structures other than the nucleus.
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Nuclear Export of mRNA02:31

Nuclear Export of mRNA

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Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
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Adult Stem Cells01:33

Adult Stem Cells

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Stem cells are undifferentiated cells that divide and produce more stem cells or progenitor cells that differentiate into mature, specialized cell types. All the cells in the body are generated from stem cells in the early embryo, but small populations of stem cells are also present in many adult tissues including the bone marrow, brain, skin, and gut. These adult stem cells typically produce the various cell types found in that tissue—to replace cells that are damaged or to continuously...
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Related Experiment Video

Updated: Feb 4, 2026

Extended Live Imaging of Female Drosophila melanogaster Germline Stem Cell Niches
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Extended Live Imaging of Female Drosophila melanogaster Germline Stem Cell Niches

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Nuclear lamina dysfunction triggers a germline stem cell checkpoint.

Lacy J Barton1,2, Tingting Duan1, Wenfan Ke1,3

  • 1Department of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.

Nature Communications
|September 29, 2018
PubMed
Summary

Nuclear lamina protein Otefin loss in Drosophila causes germline stem cell defects. Inactivating DNA damage response kinases ATR and Chk2 rescues stem cells but reveals a novel checkpoint maintaining gamete quality.

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Study of the DNA Damage Checkpoint using Xenopus Egg Extracts
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Study of the DNA Damage Checkpoint using Xenopus Egg Extracts
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Area of Science:

  • Cell Biology
  • Developmental Biology
  • Genetics

Background:

  • Nuclear lamina (NL) proteins, including LEM domain (LEM-D) proteins, are crucial for stem cell maintenance via poorly understood mechanisms.
  • Otefin (Ote), the Drosophila emerin homolog, is essential for germline stem cell (GSC) maintenance and gametogenesis.

Purpose of the Study:

  • Investigate the role of Otefin in nuclear architecture and GSC maintenance.
  • Elucidate the mechanisms underlying GSC loss and gametogenesis defects in ote mutants.
  • Identify pathways involved in regulating GSC fate and gamete quality.

Main Methods:

  • Analysis of nuclear architecture in ote mutant Drosophila germ cells.
  • Genetic inactivation of DNA damage response (DDR) kinases ATR and Chk2.
  • Assessment of GSC survival and gametogenesis rescue.
  • Cytological and genetic characterization of the GSC checkpoint.

Main Results:

  • Otefin loss leads to germ cell-specific nuclear architecture changes and GSC loss.
  • Inactivation of ATR and Chk2 rescues GSC death and gametogenesis.
  • The GSC checkpoint, though utilizing DDR components, exhibits distinct features from canonical pathways.
  • Nuclear lamina structural deformation correlates with checkpoint activation.

Conclusions:

  • Otefin-dependent nuclear lamina integrity is critical for GSC maintenance.
  • A GSC-specific checkpoint, triggered by NL dysfunction, is activated upon Otefin loss.
  • This checkpoint, involving ATR and Chk2, contributes to maintaining gamete quality, preventing the development of defective embryos.