Evidence map›Paper›PMID 41423653›Full record

ArticleJournal of animal science and biotechnology2025

BDH1 acetylation at K116 modulates milk fat production in dairy goats.

Tiantian Xiong, Chong Chen, Xinglong Gong, Chengming Han, Min Tian, Jun Luo, Lu Deng, Juan J Loor, Cong Li

Abstract read
In one paragraph

Article in Journal of animal science and biotechnology, 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Tiantian Xiong *College of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Chong Chen *College of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Xinglong GongCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Chengming HanCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Min TianCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Jun LuoCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Lu DengCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China.
Juan J LoorDepartment of Animal Sciences and Division of Nutritional Sciences, University of Illinois, Urbana, IL, 61801, USA.
Cong LiCollege of Animal Science and Technology, Northwest A&F University, Yangling, 712100, China. congl@nwafu.edu.cn.ORCID http://orcid.org/0009-0007-9282-5761

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 31702098National Key Research and Development Program of China 2022YFF1000102Xi'an Agricultural Technology Research General Project 24NYGG0025
6 · The paper itself

Abstract

backgroundGoat milk is increasingly recognized for high digestibility and a distinctive compositional profile. Protein acetylation, an important post-translational modification, regulates biosynthetic and metabolic pathways. This study aimed to identify critical acetylated proteins and specific modification sites involved in milk production and component synthesis in dairy goats, thereby elucidating the molecular mechanisms of lactation. We performed a comparative TMT-based acetylomic and proteomic analysis of mammary tissues from Saanen dairy goats during peak lactation and the dry period using LC-MS/MS. A candidate acetylation site was further investigated in goat mammary epithelial cells (GMECs) through site-directed mutagenesis and lipid metabolic assays, establishing functional links between acetylation and mammary lipid metabolism and providing a foundation for molecular strategies to improve milk quality and yield.

resultsWe established a comprehensive mammary acetylome, identifying 862 significantly acetylated proteins and 2,028 modification sites across the two physiological phases. Differentially acetylated proteins were predominantly localized to the cytoplasm (39.98%). From these, 54 key acetylated proteins, including MTOR, BCAT2, QARS1, GOT1, GOT2, BDH1, ACSS1, STAT5B, FABP5, and GPAM were prioritized as candidates involved in milk protein synthesis, milk fat synthesis, lactose synthesis, and other lactation-related processes. Among them, β-hydroxybutyrate dehydrogenase 1 (BDH1) acetylation was characterized in detail. Members of the HDAC family were identified as primary regulators mediating BDH1 deacetylation. BDH1 acetylation promoted lipid droplet formation and triglyceride synthesis in GMECs. At the transcriptional level, BDH1 acetylation upregulated LXRα, ACSL1 and SCD1, whereas deacetylation downregulated SCD1, FASN, and ACSL1. Notably, BDH1 acetylation/deacetylation significantly reduced SREBP1 expression, linking this modification to coordinated control of lipogenic gene networks.

conclusionsThis study established, for the first time, the comprehensive acetylome of mammary gland tissues in dairy goats, revealing a substantial number of differentially acetylated proteins and modification sites. We demonstrate that acetylation of BDH1 regulated by HDACs promotes lipid droplet biogenesis and triglyceride synthesis in GMECs through transcriptional modulation of key lipogenic genes and suppression of SREBP1. These findings provide mechanistic insights into the post-translational regulation of mammary lipid metabolism and offer molecular targets for future genetic and nutritional strategies aimed at enhancing milk quality and yield in dairy goats.

Indexed as

AcetylomeBDH1 proteinDairy goatFat biosynthesisModification sites

Identifiers

PMID41423653
PMCPMC12720437

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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.