Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-30T19:14:39.742Z Has data issue: false hasContentIssue false

Genomic-scale quantitative analysis of yeast pre-mRNA splicing: Implications for splice-site recognition

Published online by Cambridge University Press:  01 September 1999

PASCAL J. LOPEZ
Affiliation:
European Molecular Biology Laboratory, D-69117, Heidelberg, Germany
BERTRAND SÉRAPHIN
Affiliation:
European Molecular Biology Laboratory, D-69117, Heidelberg, Germany

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The availability of the complete sequence of the genome of Saccharomyces cerevisiae (Goffeau et al., 1996) and other organisms has provided a substantial amount of information on their chromosomal organization. We need now to understand the coordinated expression of the many genes present in a given genome and the function of the various encoded proteins. Microarrays (DNA chips) offer the opportunity to analyze nucleic acids at the genomic scale and have been used to perform global gene expression studies (Lander, 1999). However, these techniques also have the potential to give us a new perspective on posttranscriptional processes involved in the regulation of gene expression. We provide here a striking example through the investigation of yeast pre-mRNA splicing. Our analysis demonstrates that pre-mRNA splicing is quantitatively a much more important process in this species than previously thought and shows that splicing-signal conservation is correlated with transcription efficiency.

Type
LETTERS TO THE EDITOR
Information
RNA , Volume 5 , Issue 9 , September 1999 , pp. 1135 - 1137
Copyright
© 1999 RNA Society