Silencers regulate both constitutive and alternative splicing events in mammals

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

Constitutive and alternative splicing events are regulated, in higher eukaryotes, by the action of multiple weak cis-acting elements and trans-acting factors. In particular, several evidences have suggested that silencers might have a fundamental role in preventing pseudoexon inclusion in mature transcripts and in defining constitutive exons by suppressing nearby decoy splice sites. Moreover, silencer elements allow the recruitment of regulatory factors to alternatively spliced exons, therefore participating in the modulation of alternative splicing pathways. Here we focus on splicing repression mechanisms in mammals, with particular concern to both exonic and intronic silencer elements, secondary structure formation and role in human genetic disease. Recently, in addition to the availability of a growing number of sequence elements deriving from the analysis of individual regulated exons, approaches have been developed that allowed the systematic identification of splicing silencers. These methods and are briefly described, as well as the motifs they retrieved, and summary of silenced exons is provided.

Original languageEnglish
Pages (from-to)1579-1604
Number of pages26
JournalCellular and Molecular Life Sciences
Volume62
Issue number14
DOIs
Publication statusPublished - Jul 2005

Fingerprint

Mammals
Alternative Splicing
Exons
Transcriptional Silencer Elements
Inborn Genetic Diseases
Trans-Activators
Medical Genetics
Eukaryota
Modulation
Availability

Keywords

  • Alternative splicing
  • cis-acting elements
  • Constitutive splicing
  • Human genetic disease
  • Secondary structure
  • Splicing silencer
  • trans-acting factor

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Cell Biology

Cite this

Silencers regulate both constitutive and alternative splicing events in mammals. / Pozzoli, U.; Sironi, M.

In: Cellular and Molecular Life Sciences, Vol. 62, No. 14, 07.2005, p. 1579-1604.

Research output: Contribution to journalArticle

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