This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility: Researchers from Kyushu University have found that H3mm15, a histone H3.3 subvariant, contributes to normal sperm development in mice by helping regulate gene expression during spermatogenesis. The findings show that H3mm15 cannot be interchanged with conventional H3.3; although the proteins differ at only three amino acids, they behave differently in chromatin, the DNA-protein structure that packages genetic material.
Histones act like molecular spools around which DNA is wrapped, helping organize the genome and regulate gene activity. H3.3, a histone H3 variant, is incorporated into chromatin independently of DNA replication and is associated with active genomic regions. The researchers previously identified several closely related H3.3 subvariants in mice.
Among them, H3mm15 differs from conventional H3.3 at just three amino acids, and RNA analyses showed that the gene encoding H3mm15 is predominantly expressed in the testis. These observations raised a broader question: Can such small differences in histone amino acid sequence lead to distinct biological functions? In the present study, a research team led by professor Akihito Harada of the Faculty of Medical Sciences, in collaboration with Qianmei Wu, distinguished professor Yasuyuki Ohkawa of Kyushu University's Medical Institute of Bioregulation, and professor Tatsuya Takemoto of Tokushima University, investigated the function of H3mm15.
They generated H3mm15-deficient mice and assessed their testis structure, sperm motility and gene expression. The study was published online in the journal Nucleic Acids Research on Nov. 9, 2026. The team found that mice lacking H3mm15 showed disorganized seminiferous tubules—the structures in which sperm develop—as well as reduced sperm motility.
In addition, there was altered expression of spermatogenesis-related genes, particularly those associated with transition into meiosis. In cultured cells, H3mm15 was incorporated into chromatin less efficiently than H3.3 but showed relative enrichment near promoters, where gene transcription begins. Analysis of transgenic mouse testes also detected H3mm15-EGFP enrichment around transcription start sites.
Structural and biochemical analyses revealed that H3mm15 forms less stable nucleosomes, the basic units of chromatin, than H3.3. Live-cell measurements showed more dynamic chromatin association, with glutamine at position 100 contributing strongly to this behavior. However, H3mm15-containing nucleosomes did not enhance RNA polymerase II transcription in vitro under the conditions tested, suggesting that reduced nucleosome stability alone does not explain its effects on gene regulation.
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