Regulation of alternative pre-mRNA splicing by depolarization/CaMKIV

dc.contributor.authorLiu, Guodong
dc.contributor.examiningcommitteeShiu, Robert (Physiology) Amara, Francis (Biochemistry and Medical Genetics) Myal, Yvonne (Pathology) Chabot, Benoit (Université de Sherbrooke)en_US
dc.contributor.supervisorXie, Jiuyong (Physiology)en_US
dc.date.accessioned2012-12-20T22:19:27Z
dc.date.available2012-12-20T22:19:27Z
dc.date.issued2009-06-12en_US
dc.date.issued2012-06-29en_US
dc.degree.disciplinePhysiologyen_US
dc.degree.levelDoctor of Philosophy (Ph.D.)en_US
dc.description.abstractAlternative pre-mRNA splicing is often controlled by cell signals (1-3). Membrane depolarization/calcium (Ca2+) signaling controls alternative splicing of a group of genes in neurons and endocrine cells (4-9), with important implications in memory formation or secretion of hormones and neurotransmitters (10-15). However, the underlying molecular basis remains largely unknown. In rat GH3 pituitary cells, BK potassium channels control cellular electrical firing, which is critical for the release of growth hormone and prolactin. Inclusion of the STREX exon of the Slo1 gene encoding the channel α subunit is repressed by the Ca2+/calmodulin-dependent kinase IV (CaMKIV) upon depolarization (4). We isolated CaMKIV-responsive RNA elements (CaRREs) from a library of 13-nucleotide random sequences through in vivo selection in HEK293T cells. Most elements are CA-rich or A-rich, with the heterogeneous nuclear ribonucleoprotein (hnRNP) L as a binding factor. This is consistent with the finding that CA-rich elements and hnRNP L are targeted by CaMKIV in the regulation of splicing (16). In further efforts to directly link the kinase with hnRNP L, we showed that hnRNP L is essential for the full repression of STREX by depolarization and that a highly conserved CaMKIV target serine (Ser513) of L is required. Ser513 phosphorylation enhanced L binding to the STREX CaRRE1, leading to reduced binding of the constitutive factor U2AF65 to the 3’ splice site of STREX. Mutation of Ser513 abolished both activities. Therefore, hnRNP L mediates the repression of STREX by depolarization through modulation of a key step in spliceosomal assembly. We further identified hnRNP L, L-like (LL) and PTB as repressors of STREX and other depolarization-regulated exons with differential effects. Moreover, a full response of STREX to depolarization is mediated by combinations of hnRNP L and LL or PTB. Another depolarization-responsive exon, the exon 18 of the neuregulin 1 gene, is also controlled in a similar way, with the hnRNP L Ser513 required as well. This work provides the first direct link between the Ca2+ signaling and a specific serine of a regulatory splicing factor. Elucidation of the underlying molecular mechanisms would likely help us understand the fine-tuning of hormone secretion and memory formation.en_US
dc.description.noteFebruary 2013en_US
dc.identifier.citationLi, H., Liu, G., Yu, J., Cao, W., Lobo, V.G. and Xie, J. (2009) In Vivo Selection of Kinase-responsive RNA Elements Controlling Alternative Splicing. J Biol Chem, 284(24): 16191-16201en_US
dc.identifier.citationLiu, G., Razanau, A., Hai, Y., Yu, J., Sohail, M., Lobo, V.G., Chu, J., Kung, S.K. and Xie, J. (2012) A conserved serine of heterogeneous nuclear ribonucleoprotein L (hnRNP L) mediates depolarization-regulated alternative splicing of potassium channels. J Biol Chem, 287(27): 22709-22716en_US
dc.identifier.urihttp://hdl.handle.net/1993/14168
dc.language.isoengen_US
dc.publisherthe American Society for Biochemistry and Molecular Biologyen_US
dc.publisherthe American Society for Biochemistry and Molecular Biologyen_US
dc.rightsopen accessen_US
dc.subjectalternative pre-mRNA splicingen_US
dc.subjecthnRNP Len_US
dc.subjectCaMKIVen_US
dc.subjectmembrane depolarizationen_US
dc.subjectphosphorylationen_US
dc.titleRegulation of alternative pre-mRNA splicing by depolarization/CaMKIVen_US
dc.typedoctoral thesisen_US
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