HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.

Abstract
DYX1C1 was first identified as a candidate gene for dyslexia susceptibility, and its role in controlling neuronal migration during embryogenesis and effect on learning in rodents have been verified. In contrast, genetic association studies have been ambiguous in replicating its effects on dyslexia. To better understand the regulation of DYX1C1 and the possible functional role of genetic variation in the promoter of DYX1C1, we selected three single-nucleotide polymorphisms (SNPs) with predicted functional consequences or suggested associations to dyslexia for detailed study. Electrophoretic mobility shift assays suggested the allele-specific binding of the transcription factors TFII-I (to rs3743205) and Sp1 (to rs16787 and rs12899331) that could be verified by competition assays. In addition, we purified a complex of protein factors binding to the previously suggested dyslexia-related SNP, -3G/A (rs3743205). Three proteins, TFII-I, PARP1, and SFPQ, were unambiguously identified by mass spectrometry and protein sequencing. Two SNPs, rs16787 and rs3743205, showed significant allelic differences in luciferase assays. Our results show that TFII-I, PARP1, and SFPQ proteins, each previously implicated in gene regulation, form a complex controlling transcription of DYX1C1. Furthermore, allelic differences in the promoter or 5' untranslated region of DYX1C1 may affect factor binding and thus regulation of the gene.
AuthorsIsabel Tapia-Páez, Kristiina Tammimies, Satu Massinen, Ananda L Roy, Juha Kere
JournalFASEB journal : official publication of the Federation of American Societies for Experimental Biology (FASEB J) Vol. 22 Issue 8 Pg. 3001-9 (Aug 2008) ISSN: 1530-6860 [Electronic] United States
PMID18445785 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • 5' Untranslated Regions
  • Cytoskeletal Proteins
  • DNA Primers
  • DNAAF4 protein, human
  • GTF2I protein, human
  • Multiprotein Complexes
  • Nerve Tissue Proteins
  • Nuclear Proteins
  • PTB-Associated Splicing Factor
  • RNA-Binding Proteins
  • Recombinant Fusion Proteins
  • Transcription Factors, TFII
  • PARP1 protein, human
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases
Topics
  • 5' Untranslated Regions
  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • Cell Line
  • Cell Movement (genetics, physiology)
  • Cytoskeletal Proteins
  • DNA Primers (genetics)
  • Dyslexia (etiology, genetics, physiopathology)
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Humans
  • Molecular Sequence Data
  • Multiprotein Complexes
  • Nerve Tissue Proteins (genetics, physiology)
  • Neurons (physiology)
  • Nuclear Proteins (genetics, physiology)
  • PTB-Associated Splicing Factor
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases (chemistry, genetics, physiology)
  • Polymorphism, Single Nucleotide
  • Promoter Regions, Genetic
  • RNA-Binding Proteins (chemistry, genetics, physiology)
  • Recombinant Fusion Proteins (genetics, metabolism)
  • Transcription Factors, TFII (chemistry, genetics, physiology)
  • Transfection

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: