Literature DB >> 1328219

A comparative structural characterization of the human NSCL-1 and NSCL-2 genes. Two basic helix-loop-helix genes expressed in the developing nervous system.

S Lipkowitz1, V Göbel, M L Varterasian, K Nakahara, K Tchorz, I R Kirsch.   

Abstract

Human cDNA clones for NSCL-1 and NSCL-2, two basic domain helix-loop-helix (bHLH) genes expressed predominantly in the developing nervous system, were obtained from a fetal brain cDNA library. The full-length transcripts and the genomic structures were determined. The cDNAs for the two genes encode predicted proteins of similar size (133 and 135 amino acids for NSCL-1 and NSCL-2, respectively) and structure. The carboxyl-terminal 75 amino acids of the two proteins contain the bHLH motif and differ from each other by only three conservative amino acid changes, while the amino-terminal portions are markedly divergent from each other. In addition to the similar protein structure, the genes have a similar genomic organization, suggesting a close evolutionary relationship. The 5'-regulatory regions of the two genes share some features (i.e. potential TATA, CCAAT, and GATA binding sites) but also differ significantly in their G+C content. NSCL-1 is relatively G+C-rich (63%) in the sequences upstream of transcription initiation and has multiple potential binding sites for transcription factors that bind to G+C-rich sequences (e.g. AP-2). NSCL-2 is relatively A+T-rich (63%) in this region and has a potential binding site for AP1. Studies of expression in normal tissues demonstrated expression of NSCL-1 and NSCL-2 in the developing central and peripheral nervous system, most likely in developing neurons. Additional Northern analysis studies in cell lines revealed expression of these genes in some cell lines derived from tumors with neural or neuroendocrine features such as neuroblastoma, PNET, and small cell lung cancer. NSCL-1 is expressed in a larger number of these cell lines. The differences in expression may parallel differences in developmental regulation.

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Year:  1992        PMID: 1328219

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  18 in total

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Journal:  Dev Dyn       Date:  1999-07       Impact factor: 3.780

2.  The neuronal basic helix-loop-helix transcription factor NSCL-1 is dispensable for normal neuronal development.

Authors:  Markus Krüger; Thomas Braun
Journal:  Mol Cell Biol       Date:  2002-02       Impact factor: 4.272

3.  Decoding hematopoietic specificity in the helix-loop-helix domain of the transcription factor SCL/Tal-1.

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Authors:  Marcus Krüger; Karen Ruschke; Thomas Braun
Journal:  EMBO J       Date:  2004-10-07       Impact factor: 11.598

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6.  Atrophy of Müller glia and photoreceptor cells in chick retina misexpressing cNSCL2.

Authors:  C M Li; R T Yan; S Z Wang
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7.  An upstream stimulatory factor (USF) binding motif is critical for rat preprotachykinin-A promoter activity in PC12 cells.

Authors:  J M Paterson; C F Morrison; S C Mendelson; J McAllister; J P Quinn
Journal:  Biochem J       Date:  1995-09-01       Impact factor: 3.857

8.  NHLH2: at the intersection of obesity and fertility.

Authors:  Deborah J Good; Thomas Braun
Journal:  Trends Endocrinol Metab       Date:  2013-05-17       Impact factor: 12.015

9.  Predisposition to arrhythmia and autonomic dysfunction in Nhlh1-deficient mice.

Authors:  Tiziana Cogliati; Deborah J Good; Mark Haigney; Petra Delgado-Romero; Michael A Eckhaus; Walter J Koch; Ilan R Kirsch
Journal:  Mol Cell Biol       Date:  2002-07       Impact factor: 4.272

10.  Microarray-based cancer prediction using soft computing approach.

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Journal:  Cancer Inform       Date:  2009-05-26
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