CU Molecular, Cellular, and Developmental Biology
MCDB Home > faculty > FacultyPublications > Lykke-AndersenJPublications > Human Upf proteins target an mRNA for no ... wnstream of a termination codon
Document Actions

Human Upf proteins target an mRNA for no ... wnstream of a termination codon


Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon.

25

Nonsense-mediated decay (NMD) rids eukaryotic cells of aberrant mRNAs containing premature termination codons. These are discriminated from true termination codons by downstream cis-elements, such as exon-exon junctions. We describe three novel human proteins involved in NMD, hUpf2, hUpf3a, and hUpf3b. While in HeLa cell extracts these proteins are complexed with hUpf1, in intact cells hUpf3a and hUpf3b are nucleocytoplasmic shuttling proteins, hUpf2 is perinuclear, and hUpf1 cytoplasmic. hUpf3a and hUpf3b associate selectively with spliced beta-globin mRNA in vivo, and tethering of any hUpf protein to the 3'UTR of beta-globin mRNA elicits NMD. These data suggest that assembly of a dynamic hUpf complex initiates in the nucleus at mRNA exon-exon junctions and triggers NMD in the cytoplasm when recognized downstream of a translation termination site.


Lykke-Andersen J, Shu MD, Steitz JA

Cell

2000-12-22 00:00

103

7

1121-31

3' Untranslated Regions,Codon, Nonsense,Fungal Proteins,Globins,Hela Cells,Humans,Molecular Sequence Data,RNA Splicing,RNA, Messenger,RNA-Binding Proteins,Saccharomyces cerevisiae Proteins,Trans-Activators,Transfection,Yeasts,3' Untranslated Regions,Codon, Nonsense,Fungal Proteins,NMD2 protein, S cerevisiae,RNA, Messenger,RNA-Binding Proteins,Saccharomyces cerevisiae Proteins,Trans-Activators,UPF3 protein, S cerevisiae,Globins

Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, 295 Congress Avenue, New Haven, CT 06536, USA

Cell

NCI CA 16038

0092-8674


S0092-8674(00)00214-2


806

True

11163187

Jens Lykke-Andersen
University of Colorado Contact Us  |   Legal & Trademarks  |  Privacy