• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2023 Fiscal Year Annual Research Report

Elucidation of mechanisms ensuring optimal double-strand break number in meiotic cells

Research Project

Project/Area Number 21H02400
Research InstitutionKyoto University

Principal Investigator

Carlton Peter  京都大学, 生命科学研究科, 准教授 (20571813)

Project Period (FY) 2021-04-01 – 2024-03-31
Keywords減数分裂 / C. elegans / 染色体
Outline of Annual Research Achievements

Building on the results published in 2022, we continued to assess the dual functions of DSB-1 in promoting and inhibiting meiotic DNA double-strand breaks.
Our live imaging experiments with EGFP-DSB-1 revealed a droplet-like localization in early prophase nuclei, shifting to a chromosome axis localization in later prophase. We were concerned that the droplet could be the result of the dimerization of EGFP. We therefore mutated EGFP in situ to the monomeric form (mEGFP), and this showed the same patterns of localization compared to non-monomeric EGFP-DSB-1. To gain further confidence, we constructed another fusion, mScarlet-DSB-1. This localization was extremely dim in early prophase, making assessment difficult; however, in later prophase, we saw the same axial localization as EGFP-DSB-1. In summary, we have good evidence for axial localization of DSB-1, but confirmation of the droplet will require further protein fusions.
Next, to assess whether the dephosphorylation of DSB-1 by PP4 requires binding of PP4 to the FXXP domains of DSB-1, we mutated the two FXXP domains closest to the key phosphoserine residue S186 (changing F and P residues to A). We hypothesized that if these sites were necessary, then PP4 would not be able to bind to and dephosphorylate DSB-1, and so would expect to see a similar effect to removing PP4; that is, a loss of double-strand breaks. However, we saw no change in break levels in these mutants. DSB-1 has 5 FXXP sites, and so our next strategy is to mutate the other 3 sites in combination.

Research Progress Status

令和5年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

令和5年度が最終年度であるため、記入しない。

  • Research Products

    (3 results)

All 2024 2023

All Presentation (3 results) (of which Int'l Joint Research: 1 results,  Invited: 2 results)

  • [Presentation] Regulation of DNA double-strand breaks in C. elegans meiotic prophase by DSB- 12024

    • Author(s)
      CARLTON, Peter
    • Organizer
      第41回染色体ワークショップ・第22回核ダイナミクス研究会
  • [Presentation] Phosphoregulation of factors promoting DNA double-strand breaks in meiosis2023

    • Author(s)
      CARLTON, Peter
    • Organizer
      第27回DNA・組換え・修復ワークショップ
    • Int'l Joint Research / Invited
  • [Presentation] Phosphoregulation of DSB-1/Rec114 mediates control of meiotic double-strand break activity in C. elegans2023

    • Author(s)
      SATO, Aya; CARLTON, Peter
    • Organizer
      第46回日本分子生物学会年会
    • Invited

URL: 

Published: 2024-12-25  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi