Abstrakti
The neuron-specific K-Cl cotransporter (KCC2) maintains a low intracellular Cl- concentration in neurons and is necessary for fast hyperpolarizing responses to GABA and glycine. The mammalian KCC2 gene (alias Slc12a5) generates two neuron-specific isoforms by using alternative promoters and first exons. Expression of the major isoform, KCC2b, is strongly upregulated during neuronal maturation, and is modulated by neuronal activity, trauma, and neurotrophic factors. in the present study, we have focused on the regulatory influence of the upstream stimulating factors USF1 and USF2 via an E-box control element in the KCC2b promoter (E-box(KCC2b)). Electrophoretic mobility shift assay in cell lines and chromatin immunoprecipitation in neurons demonstrated binding of endogenous USF1 and USF2 to the E-box(KCC2b) element. Mutation of the E-box(KCC2b) site resulted in reduced KCC2b promoter activity in cell lines and cortical neurons. Overexpression of a dominant-negative form of USF confirmed the involvement of endogenous USF proteins in the regulation of the KCC2b gene. The results suggest that binding of USF proteins to the E-box(KCC2b) may contribute to the upregulation of KCC2b gene expression in developing brain. (C) 2008 Elsevier B.V. All rights reserved.
Alkuperäiskieli | englanti |
---|---|
Lehti | Brain Research |
Vuosikerta | 1236 |
Sivut | 8-15 |
Sivumäärä | 8 |
ISSN | 0006-8993 |
DOI - pysyväislinkit | |
Tila | Julkaistu - 2008 |
OKM-julkaisutyyppi | A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu |
Tieteenalat
- 311 Peruslääketieteet
- 118 Biotieteet
- 515 Psykologia