NIH-funded research R01 grant

How cells build the structures that make eggs and sperm

Official title: Regulation of microtubule organizing centers during mammalian gametogenesis

Funded at Henry M. Jackson Fdn for the Adv Mil/med · NIH-11322052 · Data updated 2026-11-12

This project looks at how key cell components guide egg and sperm formation to lower chromosome errors that can cause infertility or birth defects.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionHenry M. Jackson Fdn for the Adv Mil/med
NIH-funded
Lab location1 site (Bethesda, United States)
Project startJanuary 1, 2016
Project endMarch 31, 2029
Funding year2026
Award (this year)$342,762
NIH project number5R01GM117155-12
Project IDNIH-11322052 on NIH RePORTER

Who could benefit from this research

Could help

There is no current patient enrollment; the work is lab-based but is most relevant to people affected by infertility or recurrent pregnancy loss linked to chromosome abnormalities.

Less likely to help

Patients whose infertility is caused by non-chromosomal issues such as blocked fallopian tubes or pure hormonal disorders are less likely to benefit directly from this basic-science project.

What this research studies

Researchers are comparing how sperm and eggs assemble the cellular machines called microtubule organizing centers (MTOCs) that line up chromosomes during cell division. They focus on proteins that control centriole duplication and spindle formation, including PLK4 and regulators of PP2A, using advanced imaging and molecular lab techniques. The team uses mammalian lab models and new experimental tools to track MTOC dynamics across the different steps of gamete formation. Results aim to explain why eggs and sperm use different MTOC processes and how those differences can lead to aneuploidy.

Why it matters

Potential benefit: If successful, this work could clarify causes of chromosome errors in eggs and sperm and eventually inform new diagnostics or treatments for some forms of infertility and risk of birth defects.

How similar studies have gone: Prior basic-science studies have shown PLK4 is a key regulator of centriole duplication, but applying these findings to compare sperm and egg MTOC behavior is a newer direction.

Where this research is happening

  • Henry M. Jackson Fdn for the Adv Mil/med
    Bethesda, United States
    Active

Researchers

  • Principal investigator: Jordan, Philip W — Henry M. Jackson Fdn for the Adv Mil/med
  • Study coordinator: Jordan, Philip W

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About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.