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转录因子PATZ1通过控制脂肪生成因子的启动子调控位点来促进脂肪生成。

Transcription factor PATZ1 promotes adipogenesis by controlling promoter regulatory loci of adipogenic factors.

作者信息

Patel Sanil, Ganbold Khatanzul, Cho Chung Hwan, Siddiqui Juwairriyyah, Yildiz Ramazan, Sparman Njeri, Sadeh Shani, Nguyen Christy M, Wang Jiexin, Whitelegge Julian P, Fried Susan K, Waki Hironori, Villanueva Claudio J, Seldin Marcus M, Sakaguchi Shinya, Ellmeier Wilfried, Tontonoz Peter, Rajbhandari Prashant

机构信息

Diabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.

Department of Biological Chemistry, University of California, Irvine, CA, 92697, USA.

出版信息

Nat Commun. 2024 Oct 2;15(1):8533. doi: 10.1038/s41467-024-52917-y.

Abstract

White adipose tissue (WAT) is essential for lipid storage and systemic energy homeostasis. Understanding adipocyte formation and stability is key to developing therapies for obesity and metabolic disorders. Through a high-throughput cDNA screen, we identified PATZ1, a POZ/BTB and AT-Hook Containing Zinc Finger 1 protein, as an important adipogenic transcription factor. PATZ1 is expressed in human and mouse adipocyte precursor cells (APCs) and adipocytes. In cellular models, PATZ1 promotes adipogenesis via protein-protein interactions and DNA binding. PATZ1 ablation in mouse adipocytes and APCs leads to a reduced APC pool, decreased fat mass, and hypertrophied adipocytes. ChIP-Seq and RNA-seq analyses show that PATZ1 supports adipogenesis by interacting with transcriptional machinery at the promoter regions of key early adipogenic factors. Mass-spec results show that PATZ1 associates with GTF2I, with GTF2I modulating PATZ1's function during differentiation. These findings underscore PATZ1's regulatory role in adipocyte differentiation and adiposity, offering insights into adipose tissue development.

摘要

白色脂肪组织(WAT)对于脂质储存和全身能量稳态至关重要。了解脂肪细胞的形成和稳定性是开发肥胖症和代谢紊乱治疗方法的关键。通过高通量cDNA筛选,我们鉴定出PATZ1,一种含有POZ/BTB和AT钩的锌指蛋白1,作为一种重要的脂肪生成转录因子。PATZ1在人和小鼠脂肪细胞前体细胞(APC)以及脂肪细胞中表达。在细胞模型中,PATZ1通过蛋白质-蛋白质相互作用和DNA结合促进脂肪生成。小鼠脂肪细胞和APC中PATZ1的缺失导致APC池减少、脂肪量减少以及脂肪细胞肥大。ChIP-Seq和RNA-Seq分析表明,PATZ1通过与关键早期脂肪生成因子启动子区域的转录机制相互作用来支持脂肪生成。质谱结果表明,PATZ1与GTF2I相关联,GTF2I在分化过程中调节PATZ1的功能。这些发现强调了PATZ1在脂肪细胞分化和肥胖中的调节作用,为脂肪组织发育提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8e2/11447024/4ebca4abacdc/41467_2024_52917_Fig1_HTML.jpg

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