SUMMARY PARAGRAPH for CEF1
About the NineTeen Complex
The nineteen complex (for prp NineTeen associated Complex and also referred to as the NTC) is a non-snRNA containing protein complex involved in splicing of nuclear RNAs via the spliceosome. It was originally isolated as a complex containing Prp19p and at least eight other proteins that complemented the splicing defect of extracts from prp19 mutant cells (3). Subsequent work has identified the genes encoding the additional members of the complex: NTC20 (4), SNT309 (5), ISY1 (4), SYF2 (6, 7), CWC2 (8), PRP46 (8), CLF1 (7, 8), CEF1 (2), and SYF1 (7, 8). The complex appears to be conserved as mammalian cells contain a functional equivalent called the Prp19/CDC5 complex composed of a similar, though not identical, set of proteins (9). The nineteen complex associates with the assembling splicesosome during or after the dissociation of the U4 snRNA, stabilizes the U5 and U6 snRNAs in the activated spliceosomal complex that is catalytic for the first step of splicing, and remains through the second step of splicing (10, 11). Following disassembly of the spliceosome, members of the nineteen complex have been found in association with the excised intron (12, 13).
The nineteen complex also appears to be involved in control of fidelity and efficiency of splicing. Mutations in isy1 suppress the relaxed fidelity of recognition of the conserved branchpoint sequence conferred by mutations in prp16, an ATP-dependent RNA helicase required for the second step of splicing, and an isy1 null mutation decreases accuracy of 3'-splice site usage (14). In addition, cells with mutations in prp45, a protein found in association with NineTeen complex members, are defective in splicing of introns with non-canonical sequences at the branchpoint or the 5' or 3' splice sites (15). Splicing efficiency of various transcripts is differentially affected by mutations in spliceosomal components, such as PRP19, suggesting that the spliceosome can distinguish between individual transcripts and possibly use these differences to specifically regulate gene expression via control of splicing (16). Interestingly, the Drosophila crooked neck protein (the homolog of CLF1) regulates glial cell differentiation by facilitating the splicing of specific target genes (17).
Mutational and genetic analysis of several nineteen complex subunits has suggested involvement in other cellular processes in addition to splicing, such as cell cycle regulation, cytoskeletal structure, DNA repair, and vesicular transport (18, 13, 1, 6, 19, 19 20). In most cases it appears that the primary defect is in splicing and the other defects are the result of failure to remove an intron from the transcript of a gene involved in that process. However Clf1p, and possibly also Prp19p, may have other direct roles in addition to splicing.
CEF1 was identified as a homolog of the S. pombe cdc5 gene encoding a Myb-related protein, which is highly conserved and found in multiple species including H. sapiens, D. melanogaster, C. elegans, A. thaliana, and S. pombe. While initial evidence suggested that the conserved cdc5 (CEF1) gene encodes a transcription factor required for expression of genes needed for the G2/M transition (1, 21 and references therein), it has been shown that that Cef1p does not act as a transcription factor for a number of genes transcribed at G2/M, and that a cef1 null in S. cerevisiae is defective in the first step of splicing (21 and references therein). Moreover, the human CDC5 protein purifies in spliceosomal complexes. Thus, it is now clear that the role of this conserved protein is in RNA splicing via the spliceosome as a member of the NineTeen Complex.
Last updated: 2009-12-11