Evidence map›Paper›PMID 39358382›Full record

ArticleNature communications2024

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

Sanil Patel, Khatanzul Ganbold, Chung Hwan Cho, Juwairriyyah Siddiqui, Ramazan Yildiz, Njeri Sparman, Shani Sadeh, Christy M Nguyen, Jiexin Wang, Julian P Whitelegge and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Therapeutic Effect ofMicroorganisms · 2024
    Article
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

18 authors.

Sanil PatelDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0009-0002-7874-1063
Khatanzul GanboldDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Chung Hwan ChoDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0001-9666-5311
Juwairriyyah SiddiquiDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Ramazan YildizDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Njeri SparmanDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Shani SadehDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Christy M NguyenDepartment of Biological Chemistry, University of California, Irvine, CA, 92697, USA.ORCID 0000-0002-3897-6207
Jiexin WangDepartment of Pathology and Laboratory Medicine and Department of Biological Chemistry, University of California, Los Angeles, CA, 90095, USA.ORCID 0000-0003-1697-1242
Julian P WhiteleggePasarow Mass Spectrometry Laboratory, NPI-Semel Institute, University of California, Los Angeles, CA, 90095, USA.ORCID 0000-0003-2763-7733
Susan K FriedDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID 0000-0003-1101-9332
Hironori WakiDepartment of Metabolism and Endocrinology, Graduate School of Medicine, Akita University, Akita, Japan.ORCID 0000-0002-5302-9793
Claudio J VillanuevaMolecular, Cellular, and Integrative Physiology Program, and Department of Integrative Biology and Physiology, University of California, Los Angeles, CA, 90095, USA.
Marcus M SeldinDepartment of Biological Chemistry, University of California, Irvine, CA, 92697, USA.ORCID 0000-0001-8026-4759
Shinya SakaguchiMedical University of Vienna, Center for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Vienna, Austria.ORCID 0000-0002-0591-2469
Wilfried EllmeierMedical University of Vienna, Center for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Vienna, Austria.ORCID 0000-0001-8192-8481
Peter TontonozDepartment of Pathology and Laboratory Medicine and Department of Biological Chemistry, University of California, Los Angeles, CA, 90095, USA.ORCID 0000-0003-1259-0477
Prashant RajbhandariDiabetes, Obesity, and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. prashant.rajbhandari@mssm.edu.ORCID 0000-0002-8146-3861

Funding

NIDDK Network Coordinating UnitU24DK097771 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Shuibing Chen, Jeffrey S. Grethe · 2013 to 2026
$20.9M
Integrative approaches to dissection of endocrine communicationDP1DK130640 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI SELDIN, MARCUS MICHAEL · 2021 to 2025
$3.2M
Peripherally-restricted cannabinoids for cancer and chemotherapy-induced painR01CA196263 · NCI · NEW YORK UNIVERSITY · PI SCHMIDT, BRIAN L, SPIGELMAN, IGOR · 2016 to 2020
$2.6M
Decoding endocrine and paracrine communication through mammokinesDP1DK140003 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Prashant Rajbhandari · 2024 to 2026
$2.4M
Interleukin-10 mediated immune cell-adipocyte crosstalk in adipose thermogenesisR01DK136035 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Prashant Rajbhandari · 2024 to 2026
$1.9M
Immune pathways in adipose thermogenesisR01DK120851 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TONTONOZ, PETER J · 2019 to 2022
$1.8M
Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) P19930Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) P23641Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) P34407NCI NIH HHS R01 CA196263NIDDK NIH HHS DP1 DK130640NIDDK NIH HHS DP1 DK140003NIDDK NIH HHS R01 DK120851NIDDK NIH HHS R01 DK136035NIDDK NIH HHS U24 DK097771U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK120851U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK130640U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DP1DK140003U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute (National Cancer Institute Division of Cancer Epidemiology and Genetics) R01CA196263
6 · The paper itself

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.

Indexed as

AdipocytesAdipogenesisPromoter Regions, GeneticTranscription Factors3T3-L1 CellsAdipose Tissue, WhiteAnimalsCell DifferentiationFemaleGene Expression RegulationHumansKruppel-Like Transcription FactorsMaleMiceMice, Inbred C57BLNeoplasm ProteinsKruppel-Like Transcription FactorsNeoplasm ProteinsPATZ1 protein, humanRepressor ProteinsTranscription FactorsZfp278 protein, mouse

Identifiers

PMID39358382
PMCPMC11447024

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.