Snu56p is Required for Mer1p-Activated Meiotic Splicing

Department of Molecular Biology, University of Medicine and Dentistry New Jersey- School of Osteopathic Medicine, Stratford, NJ 08084, USA

^* To whom correspondence should be addressed. Email: henrymf{at}umdnj.edu.

	Abstract

Alternative or regulated splicing can be applied to genes that are transcribed, but whose products may be deleterious or unnecessary to the cell. In the yeast S. cerevisiae, positive splicing regulation occurs during meiosis in which diploid cells divide to form haploid gametes. The Mer1 protein recruits the U1 snRNP to specific pre-mRNAs permitting spliceosomal assembly and splicing. The mature transcripts are required for meiotic progression, and subsequently, sporulation. We have identified a novel allele (snu56-2) of the essential U1 snRNP protein Snu56p that exhibits a sporulation defect. Using a CUP1 reporter assay and reverse transcriptase PCR, we demonstrate that this allele specifically impairs Mer1p-activated splicing. This is not a reflection of a generally deficient spliceosome as these cells splice vegetative transcripts efficiently. Furthermore, Snu56p depletion in vivo does not significantly impact mitotic splicing. Thus, its splicing function appears limited to Mer1p-activated meiosis-specific splicing. Two hybrid studies indicate that Snu56p interacts with the other two U1 snRNP factors (Mer1p and Nam8p) required for this process. Interestingly, these two proteins do not interact suggesting that Snu56p links pre-mRNA bound Mer1p to Nam8p in the U1 snRNP. This work demonstrates that the Snu56 protein is required for splicing only during meiosis.