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Related Concept Videos

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...
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DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
DNA Damage Can Stall the Cell Cycle02:36

DNA Damage Can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
The DNA Replication Fork01:02

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An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
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Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart, a...
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S-Cdk Initiates DNA Replication

The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.

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Updated: Jul 10, 2026

Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using BrdU-ChIP-Slot-Western Technique
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ATZ-1 promotes DNA replication efficiency to maintain normal meiotic function.

Taylin E Gourley1, Luke W Molesworth1, Nethma H Waduge2

  • 1Federation University, Institute of Innovation, Science and Sustainability, Australia.

FEBS Open Bio
|July 9, 2026
PubMed
Summary

The Abnormal Transition Zone 1 (ATZ-1) protein is crucial for germline genome stability. Its absence impairs DNA replication and meiotic progression, leading to developmental defects in C. elegans.

Keywords:
DNA replicationcell cyclegerm cellsmeiosismitosisoogenesis

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Area of Science:

  • Cell Biology
  • Genetics
  • Developmental Biology

Background:

  • Precise coordination of DNA replication and meiosis is vital for germline genome stability.
  • The molecular mechanisms governing this interplay are not fully understood.

Purpose of the Study:

  • To investigate the role of Abnormal Transition Zone 1 (ATZ-1) in germline genome integrity and meiotic progression in Caenorhabditis elegans.
  • To elucidate the relationship between ATZ-1, DNA replication, and cell cycle checkpoints.

Main Methods:

  • Utilized Caenorhabditis elegans as a model organism.
  • Generated and analyzed atz-1 mutant strains.
  • Assessed germline architecture, oocyte development, S-phase DNA replication, and sensitivity to checkpoint kinase depletion (chk-1, chk-2).

Main Results:

  • Absence of ATZ-1 led to abnormal germline architecture and oocyte development.
  • atz-1 mutants exhibited depleted S-phase DNA replication.
  • Mutants showed acute sensitivity to checkpoint kinase 1 (chk-1) depletion, but not chk-2.
  • ATZ-1 appears to promote replication efficiency and suppress replication stress during premeiotic S-phase.

Conclusions:

  • ATZ-1 is essential for maintaining germline genome integrity by influencing cell cycle processes.
  • Disruption of ATZ-1 function results in significant downstream germline defects, including impaired replication and meiosis.
  • ATZ-1 plays a critical role in ensuring timely meiotic progression through efficient DNA replication.