Identification of HTRA4 as a Transcriptional Target of p63 in Trophoblast.
Humans
Trophoblasts
/ metabolism
Female
Pregnancy
Transcription Factors
/ metabolism
Serine Endopeptidases
/ metabolism
Cell Differentiation
/ genetics
Cell Line, Tumor
Tumor Suppressor Proteins
/ metabolism
Placenta
/ metabolism
Serine Proteases
/ metabolism
Promoter Regions, Genetic
/ genetics
Pre-Eclampsia
/ genetics
Transcription, Genetic
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
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
1162-1170Informations 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.