The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3

FEBS Letters ◽  
1998 ◽  
Vol 438 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Norbert Tinel ◽  
Inger Lauritzen ◽  
Christophe Chouabe ◽  
Michel Lazdunski ◽  
Marc Borsotto
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Kamoltip Laohakieat ◽  
Siriwan Isasawin ◽  
Sujinda Thanaphum

Abstract Sex determination in tephritid fruit flies involves a signaling cascade of alternatively spliced genes. The Transformer (TRA) and Transformer-2 (TRA-2) complex establishes an autoregulatory loop switching sex-specific splicing of tra pre-mRNA in females. The TRA/TRA-2 complex also regulates the sex-specific splicing of downstream effector genes, doublesex (dsx) and fruitless (fru). In Ceratitis capitata, a Maleness-on the-Y (MoY) gene modulates sex-specifically spliced Cctra pre-mRNA and results in the breakdown of the Cctra autoregulatory loop in males. In this study, the tra-2 and fru genes were characterised in two key pests, Bactrocera dorsalis and B. correcta. The tra-2 genes showed high degrees of conservation among tephritids. The complex gene organisation for each of Bdfru and Bcfru were identified. There are sex-specific and non sex-specific transcripts generated by alternative promoters as found in Drosophila melanogaster and other insects. RNAi knockdown of Bdtra transcripts showed that BdTRA controls the sex-specific splicing of Bddsx and Bdfru pre-mRNAs. Developmental expression analysis shows that multiple splice variants of Bdtra and Bctra RNAs are present before and during cellular blastoderm formation and that the mature sex-specific variants become fixed later in embryogenesis. Furthermore, the BddsxM splice variants are found in early embryos at the beginning of gastulation, but BdfruM does not appear until the larval stage. We proposed that the zygotic tra loop is initiated in both female and male embryos before becoming automatised or abolished by MoY, respectively.


2001 ◽  
Vol 17 (3) ◽  
pp. 514-520 ◽  
Author(s):  
Nikolaj Klöcker ◽  
Dominik Oliver ◽  
J.Peter Ruppersberg ◽  
Hans-Günther Knaus ◽  
Bernd Fakler

2005 ◽  
Vol 45 (8) ◽  
pp. 879 ◽  
Author(s):  
T. Vuocolo ◽  
N. E. Cockett ◽  
R. L. Tellam

The callipyge mutation in sheep results in postnatal hypertrophy and leanness of skeletal muscles in the pelvic limbs and loins. Associated changes also occur in the expression of a number of imprinted genes flanking the site of the mutation, which lies at the telomeric end of ovine chromosome 18. The transcripts from several of these genes are either spliced or undergo substantial RNA processing, sometimes in a very complex manner. The current investigation examined the effects of the callipyge mutation on the relative expression of some of these splice variants in samples taken: at birth, when the muscle hypertrophy phenotype is not expressed; and at 12 weeks of age, when the phenotype is fully apparent. It was concluded that changes in the postnatal developmental expression pattern of Dlk-1 are closely associated with the expression of the phenotype and that the callipyge mutation may promote a fetal-like gene expression program for some genes during postnatal life.


2010 ◽  
pp. NA-NA
Author(s):  
Jung-Min Kim ◽  
Ryan Beyer ◽  
Marti Morales ◽  
Stephanie Chen ◽  
Li Qian Liu ◽  
...  

2003 ◽  
Vol 45 (1) ◽  
pp. 59-70 ◽  
Author(s):  
Koichi Nakajo ◽  
You Katsuyama ◽  
Fumihito Ono ◽  
Yukio Ohtsuka ◽  
Yasushi Okamura

2002 ◽  
Vol 539 (3) ◽  
pp. 657-668 ◽  
Author(s):  
Wenli Gu ◽  
Günter Schlichthörl ◽  
Jochen R. Hirsch ◽  
Hartmut Engels ◽  
Christine Karschin ◽  
...  

2019 ◽  
Vol 19 (1S) ◽  
pp. 109-111
Author(s):  
A P Schwarz ◽  
A N Trofimov ◽  
A M Ischenko ◽  
O E Zubareva ◽  
V M Klimenko

Various detrimental factors during early life may affect CNS development and increase risk of neuropsychiatric symptoms in later life. Disruption in brain dopaminergic system maturation is believed to be one of the mechanism of different neurodevelopmental disordrers. In this article we review behavioral peculiarities and changes of prefrontal D2 dopamine receptor splice variants (D2S and D2L) expression in rats after chronic experimental increase of proinflammatory cytokine interleukin(IL)-1β during 3rd week of life. Early life IL-1β treatment produce long lasting working memory deficit originating in juvenile adult animals. Elevation of IL-1β during 3rd week of life also affect developmental expression of D2 dopamine receptor mRNAs leading to increased D2S/D2L ratio in the medial prefrontal cortex of adolescent but not adult rats. Early life IL-1β treatment cancelled the learning-induced D2L mRNA downregulation during active avoidance conditioning in adult rats. Thus, dysregulation of expression of distinct D2 dopamine receptor splice variants within medial prefrontal cortex is supposed to be implicated in cognitive decline caused by early life immune challenge.


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