<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE306nnn/GSE306673/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE306673</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Akkermansia muciniphila contributes to fasting-mediated radioprotection by inducing epigenetic and transcriptional changes in small intestinal epithelial cells</name><description>Fasting protects the small intestine epithelial cells from high-dose radiation injury, yet the mechanisms linking fasting to epithelial regeneration remain incompletely understood. Akkermansia muciniphila (AKK) is both necessary and sufficient for fasting-induced radioprotection. Selective depletion of AKK abolishes fasting-mediated preservation of SI stem cells, while recolonization restores epithelial integrity and survival. AKK produces the short-chain fatty acid propionate, which, together with host-derived β-hydroxybutyrate (β-OHB), induces histone H3 acetylation (H3K27ac, H3K9ac) and β-hydroxybutyrylation (H3K9bhb) in crypt epithelial cells, remodeling enhancer–promoter landscapes. CUT&amp;Tag and single-cell ATAC-seq analyses show that fasting, in an AKK-dependent manner, expands a Clu⁺Olfm4⁺ “revival” stem cell (persister cells) population enriched for HNF, FOXA, GATA and KLF transcription factor motifs, establishing a pro-regenerative chromatin state that persists through injury-repair phases. CTCF and BORIS activities persist, suggesting a role in maintaining epigenetic memory for intestinal regeneration after radiation. This microbiota–metabolite–chromatin axis primes persister cells for rapid regeneration after damage and offers a strategy to protect normal tissues during radiation therapy.</description><dates><publication>2026/06/08</publication></dates><accession>GSE306673</accession><cross_references><GSM>GSM9205769</GSM><GSM>GSM9205768</GSM><GSM>GSM9205789</GSM><GSM>GSM9205767</GSM><GSM>GSM9205788</GSM><GSM>GSM9205766</GSM><GSM>GSM9205783</GSM><GSM>GSM9205761</GSM><GSM>GSM9205782</GSM><GSM>GSM9205781</GSM><GSM>GSM9205780</GSM><GSM>GSM9205765</GSM><GSM>GSM9205787</GSM><GSM>GSM9205786</GSM><GSM>GSM9205764</GSM><GSM>GSM9205785</GSM><GSM>GSM9205763</GSM><GSM>GSM9205762</GSM><GSM>GSM9205784</GSM><GSM>GSM9205779</GSM><GSM>GSM9205778</GSM><GSM>GSM9205777</GSM><GSM>GSM9205772</GSM><GSM>GSM9205771</GSM><GSM>GSM9205770</GSM><GSM>GSM9205792</GSM><GSM>GSM9205791</GSM><GSM>GSM9205776</GSM><GSM>GSM9205775</GSM><GSM>GSM9205774</GSM><GSM>GSM9205773</GSM><GSM>GSM9205790</GSM><GPL>24247</GPL><GSE>306673</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>