Evidence map›Paper›PMID 38992327›Full record

ArticleCellular and molecular life sciences : CMLS2024

Lactate modulates zygotic genome activation through H3K18 lactylation rather than H3K27 acetylation.

Yanhua Zhao, Meiting Zhang, Xingwei Huang, Jiqiang Liu, Yuchen Sun, Fan Zhang, Na Zhang, Lei Lei

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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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

8 authors.

Yanhua Zhao *Department of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Meiting Zhang *Department of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Xingwei Huang *Department of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Jiqiang LiuDepartment of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Yuchen SunDepartment of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Fan ZhangDepartment of Histology and Embryology, Harbin Medical University, Harbin, 150081, China.
Na ZhangState Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China. zhangna9902@pku.edu.cn.
Lei LeiDepartment of Histology and Embryology, Harbin Medical University, Harbin, 150081, China. lei086@ems.hrbmu.edu.cn.ORCID http://orcid.org/0000-0001-5372-8749

Funding

Heilongjiang Natural Science Foundation ZD2021C005
6 · The paper itself

Abstract

In spite of its essential role in culture media, the precise influence of lactate on early mouse embryonic development remains elusive. Previous studies have implicated lactate accumulation in medium affecting histone acetylation. Recent research has underscored lactate-derived histone lactylation as a novel epigenetic modification in diverse cellular processes and diseases. Our investigation demonstrated that the absence of sodium lactate in the medium resulted in a pronounced 2-cell arrest at the late G2 phase in embryos. RNA-seq analysis revealed that the absence of sodium lactate significantly impaired the maternal-to-zygotic transition (MZT), particularly in zygotic gene activation (ZGA). Investigations were conducted employing Cut&Tag assays targeting the well-studied histone acetylation and lactylation sites, H3K18la and H3K27ac, respectively. The findings revealed a noticeable reduction in H3K18la modification under lactate deficiency, and this alteration showed a significant correlation with changes in gene expression. In contrast, H3K27ac exhibited minimal correlation. These results suggest that lactate may preferentially influence early embryonic development through H3K18la rather than H3K27ac modifications.

Indexed as

HistonesLactic AcidZygoteAcetylationAnimalsEmbryonic DevelopmentEpigenesis, GeneticFemaleGene Expression Regulation, DevelopmentalGenomeMiceProtein Processing, Post-TranslationalHistonesLactic AcidEmbryo culture mediumHistone acetylationHistone lactylationLactateZygotic genome activation (ZGA)

Identifiers

PMID38992327
PMCPMC11335220

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Registered trials

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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.