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Updated: May 7, 2026

In Vitro Biochemical Assays using Biotin Labels to Study Protein-Nucleic Acid Interactions
Published on: July 17, 2019
MEIOB targets single-strand DNA and is necessary for meiotic recombination
Benoit Souquet1, Emilie Abby, Roxane Hervé
1Univ. Paris Diderot, Sorbonne Paris Cité, Laboratory of Development of the Gonads, Unit of Stem Cells and Radiation, UMR 967, Fontenay aux Roses, France ; CEA, DSV, iRCM, SCSR, LDG, Fontenay aux Roses, France ; INSERM, Unité 967, Fontenay aux Roses, France ; Univ. Paris-Sud, UMR 967, Fontenay aux Roses, France.
Abstract:
Meiotic recombination is a mandatory process for sexual reproduction. We identified a protein specifically implicated in meiotic homologous recombination that we named: meiosis specific with OB domain (MEIOB). This protein is conserved among metazoan species and contains single-strand DNA binding sites similar to those of RPA1. Our studies in vitro revealed that both recombinant and endogenous MEIOB can be retained on single-strand DNA. Those in vivo demonstrated the specific expression of Meiob in early meiotic germ cells and the co-localization of MEIOB protein with RPA on chromosome axes. MEIOB localization in Dmc1 (-/-) spermatocytes indicated that it accumulates on resected DNA. Homologous Meiob deletion in mice caused infertility in both sexes, due to a meiotic arrest at a zygotene/pachytene-like stage. DNA double strand break repair and homologous chromosome synapsis were impaired in Meiob (-/-) meiocytes. Interestingly MEIOB appeared to be dispensable for the initial loading of recombinases but was required to maintain a proper number of RAD51 and DMC1 foci beyond the zygotene stage. In light of these findings, we propose that RPA and this new single-strand DNA binding protein MEIOB, are essential to ensure the proper stabilization of recombinases which is required for successful homology search and meiotic recombination.
Insights
A newly discovered protein, meiosis specific with OB domain (MEIOB), is crucial for successful meiotic recombination and fertility in mice. MEIOB stabilizes key proteins, ensuring proper DNA repair and homologous chromosome pairing during meiosis.
Area of Science:
- Molecular Biology
- Genetics
- Reproductive Biology
Background:
- Meiotic recombination is essential for sexual reproduction.
- The precise molecular mechanisms ensuring homologous recombination fidelity are not fully understood.
Purpose of the Study:
- To identify and characterize novel proteins involved in meiotic homologous recombination.
- To elucidate the function of the identified protein, MEIOB, in meiotic processes.
Main Methods:
- In vitro biochemical assays to assess DNA binding properties of MEIOB.
- In vivo studies including expression analysis, protein localization, and homologous gene deletion in mice.
- Analysis of meiotic progression, DNA double-strand break repair, and recombinase focus dynamics in mutant mice.
Main Results:
- MEIOB is a conserved, single-strand DNA-binding protein specifically expressed in early meiotic germ cells.
- MEIOB co-localizes with RPA on chromosome axes and accumulates on resected DNA in Dmc1-deficient spermatocytes.
- Homologous deletion of Meiob in mice leads to infertility due to meiotic arrest, impaired DNA repair, and failed homologous synapsis.
- MEIOB is required for maintaining RAD51 and DMC1 foci stability beyond the zygotene stage, though not for initial recombinase loading.
Conclusions:
- MEIOB is a novel, essential protein for successful meiotic recombination and fertility.
- MEIOB, along with RPA, plays a critical role in stabilizing recombinases for homology search and DNA repair.
- These findings provide new insights into the molecular regulation of meiotic homologous recombination.
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