The DECD box putative ATPase Sub2p is an early mRNA export factor

Current Biology

Volumn 11, Issue 21, 2001, Pages 1711-1715

  Jensen, Torben Heick ^a   Boulay, Jocelyne ^b   Rosbash, Michael ^a   Libri, Domenico ^b  

^a BRANDEIS UNIVERSITY   (United States)

^b CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

SACCHAROMYCES CEREVISIAE;

EID: 0035975969     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(01)00529-2     Document Type: Article

References (16)

1. U2AF65 recruits a novel human DEAD box protein required for the U2 snRNP-branchpoint interaction
2. Deletion of MUD2, the yeast homolog of U2AF65, can bypass the requirement for Sub2, an essential spliceosomal ATPase
3. Multiple roles for the yeast SUB2/yUAP56 gene in splicing
4. Identification and characterization of yUAP/Sub2p, a yeast homolog of the essential human pre-mRNA splicing factor hUAP56
5. Quality control of mRNA 3′-end processing is linked to the nuclear exosome
6. Pre-mRNA processing factors are required for nuclear export
7. A block to nuclear export in Saccharomyces cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription
8. Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair
9. DNA repair gene RAD3 of S. cerevisiae is essential for transcription by RNA polymerase II
10. Pre-mRNA splicing and mRNA export linked by direct interactions between UAP56 and Aly
11. Splicing factor Sub2 is required for nuclear mRNA export through its interaction with Yra1p
12. Aly, a context-dependent coactivator of LEF-1 and AML-1, is required for TCR alpha enhancer function
13. Messenger RNAs are recruited for nuclear export during transcription
14. Novel RING finger proteins Air1p and Air2p, interact with Hmt1p and inhibit the arginine methylation of Npl3p
15. A nuclear 3′-5′ exonuclease involved in mRNA degradation interacts with Poly(A) polymerase and the hnRNA protein Npl3p
16. New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae