| Literature DB >> 34108238 |
Yutao Yang1, Yueting Li1, Bo Liu1,2, Chenchen Li1, Zijin Liu1, Jiahui Deng3, Hanjiang Luo1, Xiaoxiao Li1, Jinjin Wu1, Hui Li1, Chuan-Yue Wang4, Ming Zhao5, Haohao Wu5, Francois Lallemend5, Per Svenningsson6, Tomas G M Hökfelt7, Zhi-Qing David Xu8,2.
Abstract
Galanin receptor1 (GalR1) transcript levels are elevated in the rat ventral periaqueductal gray (vPAG) after chronic mild stress (CMS) and are related to depression-like behavior. To explore the mechanisms underlying the elevated GalR1 expression, we carried out molecular biological experiments in vitro and in animal behavioral experiments in vivo. It was found that a restricted upstream region of the GalR1 gene, from -250 to -220, harbors an E-box and plays a negative role in the GalR1 promoter activity. The transcription factor Scratch2 bound to the E-box to down-regulate GalR1 promoter activity and lower expression levels of the GalR1 gene. The expression of Scratch2 was significantly decreased in the vPAG of CMS rats. Importantly, local knockdown of Scratch2 in the vPAG caused elevated expression of GalR1 in the same region, as well as depression-like behaviors. RNAscope analysis revealed that GalR1 mRNA is expressed together with Scratch2 in both GABA and glutamate neurons. Taking these data together, our study further supports the involvement of GalR1 in mood control and suggests a role for Scratch2 as a regulator of depression-like behavior by repressing the GalR1 gene in the vPAG.Entities:
Keywords: galanin; neuropeptides; stress; transcription factor; transmitter coexistence
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Year: 2021 PMID: 34108238 PMCID: PMC8214687 DOI: 10.1073/pnas.1922586118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205