» Articles » PMID: 34884614

PIAS Factors from Rainbow Trout Control NF-κB- and STAT-Dependent Gene Expression

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Dec 10
PMID 34884614
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Four 'protein inhibitors of activated STAT' (PIAS) control STAT-dependent and NF-κB-dependent immune signalling in humans. The genome of rainbow trout () contains eight genes, which encode at least 14 different transcripts that are differentially expressed in a tissue- and cell-specific manner. was the most strongly expressed variant among the analysed genes in most tissues, while was commonly low or absent. Since the knock-out of Pias factors in salmonid CHSE cells using CRISPR/Cas9 technology failed, three structurally different Pias protein variants were selected for overexpression studies in CHSE-214 cells. All three factors quenched the basal activity of an NF-κB promoter in a dose-dependent fashion, while the activity of an Mx promoter remained unaffected. Nevertheless, all three overexpressed Pias variants from trout strongly reduced the transcript level of the antiviral Stat-dependent gene in ifnγ-expressing CHSE-214 cells. Unlike , the overexpressed Pias factors modulated the transcript levels of NF-κB-dependent immune genes (mainly , , , and ) in ifnγ-expressing CHSE-214 cells in different ways. This dissimilar modulation of expression may result from the physical cooperation of the Pias proteins from trout with differential sets of interacting factors bound to distinct nuclear structures, as reflected by the differential nuclear localisation of trout Pias factors. In conclusion, this study provides evidence for the multiplication of genes and their sub-functionalisation during salmonid evolution.

Citing Articles

The complementary roles of STAT3 and STAT1 in cancer biology: insights into tumor pathogenesis and therapeutic strategies.

Wang W, Lopez McDonald M, Kim C, Ma M, Pan Z, Kaufmann C Front Immunol. 2023; 14:1265818.

PMID: 38022653 PMC: 10663227. DOI: 10.3389/fimmu.2023.1265818.


Recent Advances in Transcription Factors Biomarkers and Targeted Therapies Focusing on Epithelial-Mesenchymal Transition.

Chuang K, Chiou S, Hsu S Cancers (Basel). 2023; 15(13).

PMID: 37444447 PMC: 10340346. DOI: 10.3390/cancers15133338.


Lost and Found: The Family of NF-κB Inhibitors Is Larger than Assumed in Salmonid Fish.

van Muilekom D, Collet B, Rebl H, Zlatina K, Sarais F, Goldammer T Int J Mol Sci. 2023; 24(12).

PMID: 37373375 PMC: 10299181. DOI: 10.3390/ijms241210229.

References
1.
Valdez B, Henning D, Perlaky L, BUSCH R, Busch H . Cloning and characterization of Gu/RH-II binding protein. Biochem Biophys Res Commun. 1997; 234(2):335-40. DOI: 10.1006/bbrc.1997.6642. View

2.
Haller O, Arnheiter H, Pavlovic J, Staeheli P . The Discovery of the Antiviral Resistance Gene Mx: A Story of Great Ideas, Great Failures, and Some Success. Annu Rev Virol. 2018; 5(1):33-51. DOI: 10.1146/annurev-virology-092917-043525. View

3.
Joazeiro C, Weissman A . RING finger proteins: mediators of ubiquitin ligase activity. Cell. 2000; 102(5):549-52. DOI: 10.1016/s0092-8674(00)00077-5. View

4.
Huerta-Cepas J, Serra F, Bork P . ETE 3: Reconstruction, Analysis, and Visualization of Phylogenomic Data. Mol Biol Evol. 2016; 33(6):1635-8. PMC: 4868116. DOI: 10.1093/molbev/msw046. View

5.
Liongue C, OSullivan L, Trengove M, Ward A . Evolution of JAK-STAT pathway components: mechanisms and role in immune system development. PLoS One. 2012; 7(3):e32777. PMC: 3296744. DOI: 10.1371/journal.pone.0032777. View