Evidence map›Paper›PMID 41354937›Full record

ReviewEpigenetics & chromatin2025

Dynamic architecture of mammalian paternal chromatin: histone-to-protamine exchange and post-fertilization reprogramming.

Amir Masoud Firouzabadi, Farzaneh Fesahat, Seyed Morteza Seifati

Abstract readReview
In one paragraph

Review in Epigenetics & chromatin, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Exit from totipotency in mammals: an epigenetic perspective.Frontiers in cell and developmental biology · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Amir Masoud FirouzabadiDepartment of Biology, Ashk.C., Islamic Azad University, Ashkezar, Iran. firouzabadi.amirmasoud@gmail.com.ORCID http://orcid.org/0000-0002-1189-9037
Farzaneh FesahatReproductive Immunology Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.ORCID http://orcid.org/0000-0002-3743-4449
Seyed Morteza SeifatiDepartment of Biology, Ashk.C., Islamic Azad University, Ashkezar, Iran. seifati@iau.ac.ir.ORCID http://orcid.org/0000-0002-8505-5267

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromatin remodeling in male germ cells and after fertilization plays a pivotal role in genetic transmission and early embryonic development. During spermatogenesis, histone-based chromatin undergoes progressive reorganization: canonical histones are gradually replaced by testis-specific variants, then by transition proteins, and ultimately by highly basic protamines (PRM1 and PRM2). This hierarchical replacement, modulated by histone post-translational modifications-including hyperacetylation, ubiquitination, and dynamic methylation-and supported by molecular chaperones and chromatin remodelers, ensures the efficient compaction of paternal DNA required for sperm function and genome stability. Upon fertilization, paternal chromatin undergoes rapid decondensation as protamine disulfide bonds are reduced, allowing maternal histone incorporation. In parallel, the paternal genome experiences extensive but regulated epigenetic reprogramming, including DNA demethylation and histone modification changes, which together establish a transcriptionally permissive state for zygotic genome activation and maternal-paternal chromatin integration. This review aims to provide an overview of chromatin remodeling from the male germline to post-fertilization stages in mammals, integrating recent findings on the molecular machinery involved in histone-to-protamine replacement and its reversal during early embryogenesis. It outlines the major processes involved in histone-to-protamine exchange, protamine removal, and chromatin reorganization after fertilization, defining the scope of the review for readers. Where available, comparative data from vertebrate and invertebrate models are discussed to provide an initial perspective on the possible evolutionary conservation of these mechanisms. Clarifying these processes offers valuable insight into male fertility, early embryonic regulation, and potential epigenetic inheritance, with implications for both fundamental and applied reproductive biology.

Indexed as

ChromatinChromatin Assembly and DisassemblyHistonesProtaminesAnimalsCellular ReprogrammingEpigenesis, GeneticFertilizationHumansMaleSpermatogenesisSpermatozoaChromatinHistonesProtaminesChromatinDNA packagingEpigenetic reprogrammingHistoneProtamineSperm

Identifiers

PMID41354937
PMCPMC12751476

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.