GSBS Student Publications

Title

YRA1 autoregulation requires nuclear export and cytoplasmic Edc3p-mediated degradation of its pre-mRNA

GSBS Program

Biochemistry & Molecular Pharmacology

UMMS Affiliation

Graduate School of Biomedical Sciences; Department of Molecular Genetics and Microbiology

Date

2-24-2007

Document Type

Article

Medical Subject Headings

Active Transport, Cell Nucleus; Catalysis; Cell Nucleus; Exons; *Feedback, Biochemical; Gene Deletion; Gene Expression Regulation, Fungal; Karyopherins; Nuclear Proteins; Nucleocytoplasmic Transport Proteins; RNA Caps; RNA Precursors; RNA Splicing; *RNA Stability; RNA Transport; RNA, Fungal; RNA, Messenger; RNA-Binding Proteins; Receptors, Cytoplasmic and Nuclear; Regulatory Sequences, Nucleic Acid; Ribonucleoproteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Autoregulatory loops often provide precise control of the level of expression of specific genes that encode key regulatory proteins. Here we have defined a pathway by which Yra1p, a yeast mRNA export factor, controls its own expression. We show that YRA1 exon 1 sequences in cis and Yra1p in trans inhibit YRA1 pre-mRNA splicing and commit the pre-mRNA to nuclear export. Mex67p and Crm1p jointly promote YRA1 pre-mRNA export, and once in the cytoplasm, the pre-mRNA is degraded by a 5' to 3' decay mechanism that is dependent on the decapping activator Edc3p and on specific sequences in the YRA1 intron. These results illustrate how common steps in the nuclear processing, export, and degradation of a transcript can be uniquely combined to control the expression of a specific gene and suggest that Edc3p-mediated decay may have additional regulatory functions in eukaryotic cells.

Rights and Permissions

Citation: Mol Cell. 2007 Feb 23;25(4):559-73. Link to article on publisher's site

Related Resources

Link to article in PubMed

Journal Title

Molecular cell

PubMed ID

17317628