Identification of HTRA4 as a Transcriptional Target of p63 in Trophoblast.


Journal

The American journal of pathology
ISSN: 1525-2191
Titre abrégé: Am J Pathol
Pays: United States
ID NLM: 0370502

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 08 01 2024
revised: 12 03 2024
accepted: 27 03 2024
medline: 17 6 2024
pubmed: 17 6 2024
entrez: 16 6 2024
Statut: ppublish

Résumé

The placenta plays a crucial role in pregnancy success. ΔNp63α (p63), a transcription factor from the TP53 family, is highly expressed in villous cytotrophoblasts (CTBs), the epithelial stem cells of the human placenta, and is involved in CTB maintenance and differentiation. We examined the mechanisms of action of p63 by identifying its downstream targets. Gene expression changes were evaluated following overexpression and knockdown of p63 in the JEG3 choriocarcinoma cell line, using microarray-based RNA profiling. High-temperature requirement A4 (HTRA4), a placenta-specific serine protease involved in trophoblast differentiation and altered in preeclampsia, was identified as a gene reciprocally regulated by p63, and its expression was characterized in primary human placental tissues by RNA-sequencing and in situ hybridization. Potential p63 DNA-binding motifs were identified in the HTRA4 promoter, and p63 occupancy at some of these sites was confirmed using chromatin immunoprecipitation, followed by quantitative PCR in both JEG3 and trophoblast stem cells. These data begin to identify members of the transcriptional network downstream of p63, thus laying the groundwork for probing mechanisms by which this important transcription factor regulates trophoblast stemness and differentiation.

Identifiants

pubmed: 38880601
pii: S0002-9440(24)00159-7
doi: 10.1016/j.ajpath.2024.03.011
pii:
doi:

Substances chimiques

HtrA4 protein, human EC 3.4.-
TP63 protein, human 0
Transcription Factors 0
Serine Endopeptidases EC 3.4.21.-
Tumor Suppressor Proteins 0
Serine Proteases EC 3.4.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1162-1170

Informations de copyright

Copyright © 2024 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure Statement None declared.

Auteurs

Mary E Donohoe (ME)

Department of Pathology, University of California San Diego, La Jolla, California; Sanford Consortium for Regenerative Medicine, University of California San Diego, La Jolla, California.

Robert Morey (R)

Department of Pathology, University of California San Diego, La Jolla, California; Sanford Consortium for Regenerative Medicine, University of California San Diego, La Jolla, California.

Yingchun Li (Y)

Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado.

Donald Pizzo (D)

Department of Pathology, University of California San Diego, La Jolla, California.

Sampada Kallol (S)

Department of Pathology, University of California San Diego, La Jolla, California; Sanford Consortium for Regenerative Medicine, University of California San Diego, La Jolla, California.

Hee-Young Cho (HY)

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Republic of Korea.

Francesca Soncin (F)

Department of Pathology, University of California San Diego, La Jolla, California; Sanford Consortium for Regenerative Medicine, University of California San Diego, La Jolla, California.

Mana M Parast (MM)

Department of Pathology, University of California San Diego, La Jolla, California; Sanford Consortium for Regenerative Medicine, University of California San Diego, La Jolla, California. Electronic address: mparast@health.ucsd.edu.

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Classifications MeSH