» Articles » PMID: 28154937

Spatiotemporal Expression of Foxo4, Foxo6a, and Foxo6b in the Developing Brain and Retina Are Transcriptionally Regulated by PI3K Signaling in Zebrafish

Overview
Journal Dev Genes Evol
Specialty Biology
Date 2017 Feb 4
PMID 28154937
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The forkhead box subclass O (FoxO) family of proteins is a group of highly evolutionary conserved transcription factors that regulate various cellular processes and embryonic development. Dysregulated expressions of FOXO genes have been identified in numerous tumors and genetic disorders. The expression of FOXO/Foxo, particularly FOXO4/Foxo4 and FOXO6/Foxo6, in the developing nervous system has not been fully characterized. Here, we identified zebrafish foxo4, foxo6a, and foxo6b homologs and demonstrated that all three genes were expressed in the developing nervous system. foxo4, foxo6a, and foxo6b displayed ubiquitous expression in the brain and later in distinct brain tissues. In addition, these three genes were expressed in different retinal layers in a time-dependent manner. Furthermore, the mRNA expression of all three genes was significantly downregulated after treatment with a selective PI3-kinase (PI3K) inhibitor, LY294002. Our results suggest that foxo4, foxo6a, and foxo6b play important roles in the developing brain and retina and that the transcriptional levels of these genes are regulated by PI3-kinase signaling.

Citing Articles

Identification and Functional Analysis of Genes in Chinese Tongue Sole ().

Zhang T, Zhang M, Sun Y, Li L, Cheng P, Li X Int J Mol Sci. 2023; 24(8).

PMID: 37108789 PMC: 10142177. DOI: 10.3390/ijms24087625.


Identification of key miRNAs and genes for mouse retinal development using a linear model.

Wang Y, Wang X, Jiang Y, Liu R, Cao D, Pan J Mol Med Rep. 2020; 22(1):494-506.

PMID: 32319662 PMC: 7248464. DOI: 10.3892/mmr.2020.11082.


LncRNA-SULT1C2A regulates Foxo4 in congenital scoliosis by targeting rno-miR-466c-5p through PI3K-ATK signalling.

Chen C, Tan H, Bi J, Li L, Rong T, Lin Y J Cell Mol Med. 2019; 23(7):4582-4591.

PMID: 31044535 PMC: 6584475. DOI: 10.1111/jcmm.14355.

References
1.
Essaghir A, Dif N, Marbehant C, Coffer P, Demoulin J . The transcription of FOXO genes is stimulated by FOXO3 and repressed by growth factors. J Biol Chem. 2009; 284(16):10334-42. PMC: 2667720. DOI: 10.1074/jbc.M808848200. View

2.
Xie X, Liu J, Hu B, Xiao W . Zebrafish foxo3b negatively regulates canonical Wnt signaling to affect early embryogenesis. PLoS One. 2011; 6(9):e24469. PMC: 3168510. DOI: 10.1371/journal.pone.0024469. View

3.
Knight Z . Small molecule inhibitors of the PI3-kinase family. Curr Top Microbiol Immunol. 2010; 347:263-78. DOI: 10.1007/82_2010_44. View

4.
Hosaka T, Biggs 3rd W, Tieu D, Boyer A, Varki N, Cavenee W . Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification. Proc Natl Acad Sci U S A. 2004; 101(9):2975-80. PMC: 365730. DOI: 10.1073/pnas.0400093101. View

5.
Katoh M, Igarashi M, Fukuda H, Nakagama H, Katoh M . Cancer genetics and genomics of human FOX family genes. Cancer Lett. 2012; 328(2):198-206. DOI: 10.1016/j.canlet.2012.09.017. View