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Regulation and Target Specificity of Human Alternative Splicing Factors SF2/ASF and Fox-1/2

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dc.contributor.advisor Tan, Wei en_US
dc.contributor.author Sun, Shuying en_US
dc.contributor.other Department of Molecular and Cellular Biology en_US
dc.date.accessioned 2012-05-15T18:07:02Z
dc.date.available 2012-05-15T18:07:02Z
dc.date.issued 1-May-10 en_US
dc.date.submitted May-10 en_US
dc.identifier Sun_grad.sunysb_0771E_10035.pdf en_US
dc.identifier.uri http://hdl.handle.net/1951/55637
dc.description.abstract Alternative splicing is a highly regulated process in eukaryotes. It greatly increases the diversity of proteins encoded by the genome, and its disruption can cause a number of genetic diseases. SF2/ASF is a prototypical serine/arginine-rich (SR) protein, with important roles in constitutive and alternative splicing and other aspects of mRNA metabolism. SFRS1 (SF2/ASF) is a potent proto-oncogene with abnormal expression in many tumors. I found that SF2/ASF negatively autoregulates its expression to maintain homeostatic levels of the protein. I characterized six SF2/ASF alternatively spliced mRNA isoforms: the major isoform encodes full-length protein, whereas the others are either retained in the nucleus or degraded by NMD. Unproductive splicing accounts for only part of the autoregulation, which occurs primarily at the translational level. The effect is specific to SF2/ASF and requires RRM2, the second of two RNA-recognition motifs. The ultraconserved 3'UTR (untranslated region) is necessary and sufficient for downregulation. SF2/ASF overexpression shifts the distribution of target mRNA towards mono-ribosomes, and translational repression is partly independent of Dicer and a 5' cap. Thus, multiple post-transcriptional and translational mechanisms are involved in fine-tuning the expression of SF2/ASF. Fox-1 and Fox-2 are brain- and muscle-specific alternative splicing factors. Their single RRM is conserved from worm to human, and specifically binds the RNA element UGCAUG. Fox-1/2 regulate alternative splicing positively or negatively in a position-dependent manner: they activate exon inclusion when binding to the downstream intron, and promote exon skipping when binding to the upstream intron. I explored the mechanisms of splicing activation and repression by Fox-1. I found that Fox-1 can enhance exon inclusion of a heterologous gene when tethered to the downstream intron by a phage MS2 hairpin/coat-protein interaction, and its C-terminal domain is sufficient for this activity. However, both the RRM and the C-terminal domain are required for exon repression when tethered to the upstream intron. I used immunoprecipitation and mass spectrometry to identify proteins that interact with the C-terminal domain of Fox-1. Characterization of several interacting candidates to elucidate their potential roles in alternative splicing regulation by Fox-1 is in progress.We also applied Solexa high-throughput mRNA sequencing to assess global changes of alternative splicing controlled by Fox-2. We generated ~110 million paired-end reads to compare target-isoform expression levels in cells expressing Fox-2 versus cells treated by RNAi to reduce Fox-2 expression. We identified about 150 high-confidence alternative exons with Fox-dependent splicing, of which 95% could be experimentally validated. Taken together, my studies provide insights about the regulatory mechanisms involving two kinds of human splicing factors, and have broad implications for post-transcriptional control of gene expression and its misregulation in disease. en_US
dc.description.sponsorship Stony Brook University Libraries. SBU Graduate School in Department of Molecular and Cellular Biology. Lawrence Martin (Dean of Graduate School). en_US
dc.format Electronic Resource en_US
dc.language.iso en_US en_US
dc.publisher The Graduate School, Stony Brook University: Stony Brook, NY. en_US
dc.subject.lcsh Biology, Molecular en_US
dc.subject.other Fox-1/2, SF2/ASF, Splicing en_US
dc.title Regulation and Target Specificity of Human Alternative Splicing Factors SF2/ASF and Fox-1/2 en_US
dc.type Dissertation en_US
dc.description.advisor Advisor(s): Adrian R. Krainer. Committee Member(s): Senthil Muthuswamy; David L. Spector; Linda Van Aelst; Rui-Ming Xu. en_US
dc.mimetype Application/PDF en_US
dc.embargo.release 5/1/12 en_US
dc.embargo.period 2 Years en_US


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