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Heterogeneous nuclear ribonucleoprotein G regulates splice site selection by binding to CC(A/C)-rich regionsin pre-mRNA

  • Bettina Heinrich
  • , Zhaiyi Zhang
  • , Oleg Raitskin
  • , Michael Hiller
  • , Natalya Benderska
  • , Annette M. Hartmann
  • , Laurent Bracco
  • , David Elliott
  • , Shani Ben-Ari
  • , Hermona Soreq
  • , Joseph Sperling
  • , Ruth Sperling
  • , Stefan Stamm

Producción científica: Articlerevisión exhaustiva

89 Citas (Scopus)

Resumen

Almost every protein-coding gene undergoes pre-mRNA splicing, and the majority of these pre-mRNAs are alternatively spliced. Alternative exon usage is regulated by the transient formation of protein complexes on the pre-mRNA that typically contain heterogeneous nuclear ribonucleoproteins (hnRNPs). Here we characterize hnRNP G, a member of the hnRNP class of proteins. We show that hnRNP G is a nuclear protein that is expressed in different concentrations in various tissues and that interacts with other splicing regulatory proteins. hnRNP G is part of the supraspliceosome, where it regulates alternative splice site selection in a concentration-dependent manner. Its action on alternative exons can occur without a functional RNA-recognition motif by binding to other splicing regulatory proteins. The RNA-recognition motif of hnRNP G binds to a loose consensus sequence containing a CC(A/C) motif, and hnRNP G preferentially regulates alternative exons where this motif is clustered in close proximity. The X-chromosomally encoded hnRNP G regulates different RNAs than its Y-chromosomal paralogue RNA-binding motif protein, Y-linked (RBMY), suggesting that differences in alternative splicing, evoked by the sex-specific expression of hnRNP G and RBMY, could contribute to molecular sex differences in mammals.

Idioma originalEnglish
Páginas (desde-hasta)14303-14315
Número de páginas13
PublicaciónJournal of Biological Chemistry
Volumen284
N.º21
DOI
EstadoPublished - may 22 2009

Financiación

FinanciadoresNúmero del financiador
National Center for Research ResourcesP20RR020171

    ASJC Scopus subject areas

    • Biochemistry
    • Molecular Biology
    • Cell Biology

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