Genetic, epigenetic and posttranscriptional mechanisms for treatment of major depression: the 5-HT1A receptor gene as a paradigm

PR Albert, B Le François, F Vahid-Ansari - Journal of psychiatry and …, 2019 - jpn.ca
Major depression and anxiety are highly prevalent and involve chronic dysregulation of
serotonin, but they remain poorly understood. Here, we review novel transcriptional (genetic …

[HTML][HTML] Aryl hydrocarbon receptor as a DNA methylation reader in the stress response pathway

W Habano, T Miura, J Terashima, S Ozawa - Toxicology, 2022 - Elsevier
The aryl hydrocarbon receptor (AhR) mediates various cellular responses upon exposure to
exogenous and endogenous stress factors. In these responses, AhR plays a dual role as a …

[HTML][HTML] Loss of MeCP2 in adult 5-HT neurons induces 5-HT1A autoreceptors, with opposite sex-dependent anxiety and depression phenotypes

TJ Philippe, F Vahid-Ansari, ZR Donaldson… - Scientific Reports, 2018 - nature.com
The 5-HT1A autoreceptor mediates feedback inhibition of serotonin (5-HT) neurons, and is
implicated in major depression. The human 5-HT1A gene (HTR1A) rs6295 risk allele …

[HTML][HTML] DNA methylation mediates BmDeaf1-regulated tissue- and stage-specific expression of BmCHSA-2b in the silkworm, Bombyx mori

G Xu, J Zhang, H Lyu, Q Song, Q Feng, H Xiang… - Epigenetics & …, 2018 - Springer
Background Accurate regulation of tissue-and stage-specific expression of genes is
prerequisite for normal development in organisms. DNA methylation plays an important role …

Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1‐associated neurodevelopmental disorder (DAND) …

L Chen, PJ Jensik, JT Alaimo, M Walkiewicz… - Human …, 2017 - Wiley Online Library
Deformed epidermal autoregulatory factor‐1 (DEAF1), a transcription factor essential for
central nervous system and early embryonic development, has recently been implicated in a …

Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders

SR McGee, S Rajamanickam, S Adhikari… - Human molecular …, 2023 - academic.oup.com
De novo deleterious and heritable biallelic mutations in the DNA binding domain (DBD) of
the transcription factor deformed epidermal autoregulatory factor 1 (DEAF1) result in a …

[HTML][HTML] On the NF-Y regulome as in ENCODE (2019)

M Ronzio, A Bernardini, G Pavesi… - PLoS Computational …, 2020 - journals.plos.org
NF-Y is a trimeric Transcription Factor-TF-which binds with high selectivity to the conserved
CCAAT element. Individual ChIP-seq analysis as well as ENCODE have progressively …

Functional Characterization of A Deformed Epidermal Autoregulatory Factor 1 Gene in Litopenaeus vannamei

QM Hong, XJ Yang, ME Zhang, Q Chen… - Developmental & …, 2024 - Elsevier
Innate immunity is crucial for invertebrate defense against pathogenic infections. Numerous
studies have indicated that the Toll–NF–κB pathway plays an important role in this process …

[HTML][HTML] Predicted protein interactions of IFITMs may shed light on mechanisms of Zika virus-induced microcephaly and host invasion

MK Ganapathiraju, KB Karunakaran… - …, 2016 - ncbi.nlm.nih.gov
After the first reported case of Zika virus (ZIKV) in Brazil, in 2015, a significant increase in the
reported cases of microcephaly was observed. Microcephaly is a neurological condition in …

[HTML][HTML] Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain

L Chen, Y Tao, F Song, X Yuan, J Wang, D Saffen - Scientific Reports, 2016 - nature.com
Abstract RAI1 (retinoic acid induced-1) is a dosage-sensitive gene that causes Smith-
Magenis syndrome (SMS) when mutated or deleted and Potocki-Lupski Syndrome (PTLS) …