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Identification of Tbr‐1/CASK complex target genes in neurons

Tbr‐1, a neuron‐specific T‐box transcription factor, plays a critical role in brain development. Here, we performed a computational search using the non‐palindromic T‐box binding sequence, namely the non‐palindromic T‐element, to determine the putative downstream target genes of Tbr‐1. More than 20...

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Published in:Journal of neurochemistry 2004-12, Vol.91 (6), p.1483-1492
Main Authors: Wang, Ting‐Fang, Ding, Chia‐Nung, Wang, Guey‐Shin, Luo, Shih‐Chi, Lin, Yi‐Ling, Ruan, Youlin, Hevner, Robert, Rubenstein, John L. R., Hsueh, Yi‐Ping
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cited_by cdi_FETCH-LOGICAL-c4635-8abbb91c3373c0c5af7d9d43df00e46eae205b05104f7c4ccbb986510416901e3
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container_issue 6
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container_title Journal of neurochemistry
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creator Wang, Ting‐Fang
Ding, Chia‐Nung
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Rubenstein, John L. R.
Hsueh, Yi‐Ping
description Tbr‐1, a neuron‐specific T‐box transcription factor, plays a critical role in brain development. Here, we performed a computational search using the non‐palindromic T‐box binding sequence, namely the non‐palindromic T‐element, to determine the putative downstream target genes of Tbr‐1. More than 20 identified genes containing the non‐palindromic T‐element in the 5′ regulatory region were found expressed in brain. Luciferase reporter assays using cultured hippocampal neurons showed that overexpression of Tbr‐1 and CASK‐enhanced promoter activities of some of these putative target genes, including NMDAR subunit 2b (NR2b), glycine transporter, interleukin 7 receptor (IL‐7R) and OX‐2. Among these genes, NR2b promoter responded strongest to overexpression of Tbr‐1 and CASK. Deletion of the non‐palindromic T‐elements from NR2b promoter impaired the induction by Tbr‐1 and CASK. We also examined expression of these target genes in Tbr‐1 knockout mice, it was found that NR2b expression was consistently downregulated. Similarly, both RNA and protein expression levels of NMDAR subunit 1 (NR1), which also contains the non‐palindromic T‐elements in its 5′ regulatory region, were reduced in Tbr‐1 knockout mice. We suggest that Tbr‐1/CASK protein complex regulates expression of these downstream target genes and thus modulates neuronal activity and function.
doi_str_mv 10.1111/j.1471-4159.2004.02845.x
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Among these genes, NR2b promoter responded strongest to overexpression of Tbr‐1 and CASK. Deletion of the non‐palindromic T‐elements from NR2b promoter impaired the induction by Tbr‐1 and CASK. We also examined expression of these target genes in Tbr‐1 knockout mice, it was found that NR2b expression was consistently downregulated. Similarly, both RNA and protein expression levels of NMDAR subunit 1 (NR1), which also contains the non‐palindromic T‐elements in its 5′ regulatory region, were reduced in Tbr‐1 knockout mice. 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R.</au><au>Hsueh, Yi‐Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Tbr‐1/CASK complex target genes in neurons</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2004-12</date><risdate>2004</risdate><volume>91</volume><issue>6</issue><spage>1483</spage><epage>1492</epage><pages>1483-1492</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>Tbr‐1, a neuron‐specific T‐box transcription factor, plays a critical role in brain development. Here, we performed a computational search using the non‐palindromic T‐box binding sequence, namely the non‐palindromic T‐element, to determine the putative downstream target genes of Tbr‐1. More than 20 identified genes containing the non‐palindromic T‐element in the 5′ regulatory region were found expressed in brain. Luciferase reporter assays using cultured hippocampal neurons showed that overexpression of Tbr‐1 and CASK‐enhanced promoter activities of some of these putative target genes, including NMDAR subunit 2b (NR2b), glycine transporter, interleukin 7 receptor (IL‐7R) and OX‐2. Among these genes, NR2b promoter responded strongest to overexpression of Tbr‐1 and CASK. Deletion of the non‐palindromic T‐elements from NR2b promoter impaired the induction by Tbr‐1 and CASK. We also examined expression of these target genes in Tbr‐1 knockout mice, it was found that NR2b expression was consistently downregulated. Similarly, both RNA and protein expression levels of NMDAR subunit 1 (NR1), which also contains the non‐palindromic T‐elements in its 5′ regulatory region, were reduced in Tbr‐1 knockout mice. We suggest that Tbr‐1/CASK protein complex regulates expression of these downstream target genes and thus modulates neuronal activity and function.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15584924</pmid><doi>10.1111/j.1471-4159.2004.02845.x</doi><tpages>10</tpages></addata></record>
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source Wiley-Blackwell Read & Publish Collection; Free Full-Text Journals in Chemistry
subjects Amino Acid Transport Systems, Neutral - genetics
Animals
Antigens, CD
Antigens, Surface - genetics
Base Sequence
Biological and medical sciences
Calcium-Calmodulin-Dependent Protein Kinases - physiology
Cells, Cultured
Cercopithecus aethiops
COS Cells
development
Development. Senescence. Regeneration. Transplantation
DNA-Binding Proteins - physiology
Embryo, Mammalian
forebrain
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation
Glycine Plasma Membrane Transport Proteins
Guanylate Kinases
Hippocampus - cytology
Humans
membrane associated guanylate kinase
Mice
Mice, Knockout
Molecular Sequence Data
neurite
Neurons - metabolism
N‐methyl‐D‐aspartate
Promoter Regions, Genetic - physiology
Rats
Receptors, Interleukin-7 - genetics
Receptors, N-Methyl-D-Aspartate - genetics
transcription
Vertebrates: nervous system and sense organs
title Identification of Tbr‐1/CASK complex target genes in neurons
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