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1.
Nucleic Acids Res ; 46(22): 12126-12138, 2018 12 14.
Article in English | MEDLINE | ID: mdl-30335160

ABSTRACT

The active 3D conformation of the spliceosome's catalytic U2/U6 RNA core is stabilised by a network of secondary and tertiary RNA interactions, but also depends on spliceosomal proteins for its formation. To determine the contribution towards splicing of specific RNA secondary and tertiary interactions in the U2/U6 RNA core, we introduced mutations in critical U6 nucleotides and tested their effect on splicing using a yeast in vitro U6 depletion/complementation system. Elimination of selected RNA tertiary interactions involving the U6 catalytic triad, or deletions of the bases of U6-U80 or U6-A59, had moderate to no effect on splicing, showing that the affected secondary and tertiary interactions are not required for splicing catalysis. However, removal of the base of U6-G60 of the catalytic triad completely blocked splicing, without affecting assembly of the activated spliceosome or its subsequent conversion into a B*-like complex. Our data suggest that the catalytic configuration of the RNA core that allows catalytic metal M1 binding can be maintained by Protein-RNA contacts. However, RNA stacking interactions in the U2/U6 RNA core are required for productive coordination of metal M2. The functional conformation of the U2/U6 RNA core is thus highly buffered, with overlapping contributions from RNA-RNA and Protein-RNA interactions.


Subject(s)
Nucleic Acid Conformation , RNA Splicing , RNA, Fungal/chemistry , RNA, Small Nuclear/chemistry , Spliceosomes/genetics , Binding Sites , Catalysis , Catalytic Domain , Cryoelectron Microscopy , Crystallography, X-Ray , Humans , Hydrogen Bonding , Metals/chemistry , Mutation , RNA Precursors/chemistry , RNA, Messenger/metabolism , Saccharomyces cerevisiae
2.
Genes Dev ; 31(23-24): 2416-2429, 2017 12 01.
Article in English | MEDLINE | ID: mdl-29330354

ABSTRACT

The precise function of the trimeric retention and splicing (RES) complex in pre-mRNA splicing remains unclear. Here we dissected the role of RES during the assembly and activation of yeast spliceosomes. The efficiency of pre-mRNA splicing was significantly lower in the absence of the RES protein Snu17, and the recruitment of its binding partners, Pml1 (pre-mRNA leakage protein 1) and Bud13 (bud site selection protein 13), to the spliceosome was either abolished or substantially reduced. RES was not required for the assembly of spliceosomal B complexes, but its absence hindered efficient Bact complex formation. ΔRES spliceosomes were no longer strictly dependent on Prp2 activity for their catalytic activation, suggesting that they are structurally compromised. Addition of Prp2, Spp2, and UTP to affinity-purified ΔRES B or a mixture of B/Bact complexes formed on wild-type pre-mRNA led to their disassembly. However, no substantial disassembly was observed with ΔRES spliceosomes formed on a truncated pre-mRNA that allows Prp2 binding but blocks its activity. Thus, in the absence of RES, Prp2 appears to bind prematurely, leading to the disassembly of the ΔRES B complexes to which it binds. Our data suggest that Prp2 can dismantle B complexes with an aberrant protein composition, suggesting that it may proofread the spliceosome's RNP structure prior to activation.


Subject(s)
RNA Splicing/genetics , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolism , Spliceosomes/metabolism , DEAD-box RNA Helicases/metabolism , Protein Multimerization/genetics , RNA Precursors/metabolism , Ribonucleoprotein, U2 Small Nuclear/genetics , Ribonucleoprotein, U2 Small Nuclear/metabolism , Ribonucleoprotein, U4-U6 Small Nuclear/metabolism , Spliceosomes/genetics
3.
Mol Cell ; 62(4): 603-17, 2016 05 19.
Article in English | MEDLINE | ID: mdl-27184079

ABSTRACT

Identifying pairwise RNA-RNA interactions is key to understanding how RNAs fold and interact with other RNAs inside the cell. We present a high-throughput approach, sequencing of psoralen crosslinked, ligated, and selected hybrids (SPLASH), that maps pairwise RNA interactions in vivo with high sensitivity and specificity, genome-wide. Applying SPLASH to human and yeast transcriptomes revealed the diversity and dynamics of thousands of long-range intra- and intermolecular RNA-RNA interactions. Our analysis highlighted key structural features of RNA classes, including the modular organization of mRNAs, its impact on translation and decay, and the enrichment of long-range interactions in noncoding RNAs. Additionally, intermolecular mRNA interactions were organized into network clusters and were remodeled during cellular differentiation. We also identified hundreds of known and new snoRNA-rRNA binding sites, expanding our knowledge of rRNA biogenesis. These results highlight the underexplored complexity of RNA interactomes and pave the way to better understanding how RNA organization impacts biology.


Subject(s)
High-Throughput Nucleotide Sequencing/methods , RNA, Fungal/genetics , RNA, Messenger/genetics , RNA, Neoplasm/genetics , RNA, Ribosomal/genetics , RNA, Small Nucleolar/genetics , Saccharomyces cerevisiae/genetics , Transcriptome , Binding Sites , Cell Differentiation , Computational Biology , Cross-Linking Reagents/chemistry , Databases, Genetic , Embryonic Stem Cells/metabolism , Ficusin/chemistry , Gene Expression Regulation, Fungal , Gene Expression Regulation, Neoplastic , Genome-Wide Association Study , HeLa Cells , Humans , Nucleic Acid Conformation , RNA Stability , RNA, Fungal/chemistry , RNA, Fungal/metabolism , RNA, Messenger/chemistry , RNA, Messenger/metabolism , RNA, Neoplasm/chemistry , RNA, Neoplasm/metabolism , RNA, Ribosomal/chemistry , RNA, Ribosomal/metabolism , RNA, Small Nucleolar/chemistry , RNA, Small Nucleolar/metabolism , Ribosomes/genetics , Ribosomes/metabolism , Saccharomyces cerevisiae/metabolism
4.
RNA Biol ; 13(3): 320-30, 2016.
Article in English | MEDLINE | ID: mdl-26821976

ABSTRACT

A rapidly increasing number of RNA helicases are implicated in several distinct cellular processes, however, the modes of regulation of multifunctional RNA helicases and their recruitment to different target complexes have remained unknown. Here, we show that the distribution of the multifunctional DEAH-box RNA helicase Prp43 between its diverse cellular functions can be regulated by the interplay of its G-patch protein cofactors. We identify the orphan G-patch protein Cmg1 (YLR271W) as a novel cofactor of Prp43 and show that it stimulates the RNA binding and ATPase activity of the helicase. Interestingly, Cmg1 localizes to the cytoplasm and to the intermembrane space of mitochondria and its overexpression promotes apoptosis. Furthermore, our data reveal that different G-patch protein cofactors compete for interaction with Prp43. Changes in the expression levels of Prp43-interacting G-patch proteins modulate the cellular localization of Prp43 and G-patch protein overexpression causes accumulation of the helicase in the cytoplasm or nucleoplasm. Overexpression of several G-patch proteins also leads to defects in ribosome biogenesis that are consistent with withdrawal of the helicase from this pathway. Together, these findings suggest that the availability of cofactors and the sequestering of the helicase are means to regulate the activity of multifunctional RNA helicases and their distribution between different cellular processes.


Subject(s)
DEAD-box RNA Helicases/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Apoptosis , Cell Nucleus/metabolism , Cytoplasm/metabolism , Gene Expression Regulation, Fungal , Mitochondrial Membranes/metabolism , Signal Transduction
5.
Sci Rep ; 5: 11282, 2015 Jun 15.
Article in English | MEDLINE | ID: mdl-26074133

ABSTRACT

Trimethylguanosine Synthase catalyses transfer of two methyl groups to the m(7)G cap of RNA polymerase II transcribed snRNAs, snoRNAs, and telomerase RNA TLC1 to form a 2,2,7-trimethylguanosine cap. While in vitro studies indicate that Tgs1 functions as a monomer and the dimethylation of m(7)G caps is not a processive reaction, partially methylated sn(o)RNAs are typically not detected in living cells. Here we show that both yeast and human Tgs1p possess a conserved self-association property located at the N-terminus. A disruption of Tgs1 self-association led to a strong reduction of sn(o)RNA trimethylation as well as reduced nucleolar enrichment of Tgs1. Self-association of Tgs1p and its catalytic activity were also prerequisite to bypass the requirement for its accessory factor Swm2p for efficient pre-rRNA processing and snRNA trimethylation. The ability to self-associate might enable Tgs1 to efficiently dimethylate the caps of the targeted RNAs in vivo.


Subject(s)
Methyltransferases/genetics , RNA Precursors/genetics , RNA, Small Nucleolar/genetics , Saccharomyces cerevisiae/genetics , Carrier Proteins/genetics , Carrier Proteins/metabolism , Escherichia coli/genetics , Escherichia coli/metabolism , Gene Expression , Guanosine/analogs & derivatives , Guanosine/biosynthesis , Humans , Methylation , Methyltransferases/chemistry , Methyltransferases/metabolism , Protein Structure, Tertiary , RNA Precursors/metabolism , RNA Splicing , RNA, Small Nucleolar/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism , Signal Transduction , Transcription, Genetic
6.
Nat Methods ; 11(10): 1064-70, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25173706

ABSTRACT

RNA-protein complexes play pivotal roles in many central biological processes. Although methods based on high-throughput sequencing have advanced our ability to identify the specific RNAs bound by a particular protein, there is a need for precise and systematic ways to identify RNA interaction sites on proteins. We have developed an experimental and computational workflow combining photo-induced cross-linking, high-resolution mass spectrometry and automated analysis of the resulting mass spectra for the identification of cross-linked peptides, cross-linking sites and the cross-linked RNA oligonucleotide moieties of such RNA-binding proteins. The workflow can be applied to any RNA-protein complex of interest or to whole proteomes. We applied the approach to human and yeast mRNA-protein complexes in vitro and in vivo, demonstrating its powerful utility by identifying 257 cross-linking sites on 124 distinct RNA-binding proteins. The open-source software pipeline developed for this purpose, RNP(xl), is available as part of the OpenMS project.


Subject(s)
Mass Spectrometry/methods , RNA-Binding Proteins/chemistry , RNA/chemistry , Amino Acids/chemistry , Automation , Binding Sites , Computer Simulation , Cross-Linking Reagents/chemistry , Fungal Proteins/chemistry , Humans , Oligonucleotides/chemistry , Peptides/chemistry , Proteome , Proteomics/methods , Software
7.
Genes Dev ; 27(4): 413-28, 2013 Feb 15.
Article in English | MEDLINE | ID: mdl-23431055

ABSTRACT

The spliceosome is a single-turnover enzyme that needs to be dismantled after catalysis to both release the mRNA and recycle small nuclear ribonucleoproteins (snRNPs) for subsequent rounds of pre-mRNA splicing. The RNP remodeling events occurring during spliceosome disassembly are poorly understood, and the composition of the released snRNPs are only roughly known. Using purified components in vitro, we generated post-catalytic spliceosomes that can be dissociated into mRNA and the intron-lariat spliceosome (ILS) by addition of the RNA helicase Prp22 plus ATP and without requiring the step 2 proteins Slu7 and Prp18. Incubation of the isolated ILS with the RNA helicase Prp43 plus Ntr1/Ntr2 and ATP generates defined spliceosomal dissociation products: the intron-lariat, U6 snRNA, a 20-25S U2 snRNP containing SF3a/b, an 18S U5 snRNP, and the "nineteen complex" associated with both the released U2 snRNP and intron-lariat RNA. Our system reproduces the entire ordered disassembly phase of the spliceosome with purified components, which defines the minimum set of agents required for this process. It enabled us to characterize the proteins of the ILS by mass spectrometry and identify the ATPase action of Prp43 as necessary and sufficient for dissociation of the ILS without the involvement of Brr2 ATPase.


Subject(s)
RNA Splicing , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolism , Spliceosomes/metabolism , DEAD-box RNA Helicases/metabolism , Introns , RNA Splicing Factors , RNA, Messenger/metabolism , RNA, Small Nuclear/metabolism , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/metabolism , Spliceosomes/chemistry
8.
FEBS Lett ; 584(15): 3299-304, 2010 Aug 04.
Article in English | MEDLINE | ID: mdl-20621096

ABSTRACT

The 5' cap trimethylation of small nuclear (snRNAs) and several nucleolar RNAs (snoRNAs) by trimethylguanosine synthase 1 (Tgs1p) is required for efficient pre-mRNA splicing. The previously uncharacterised protein Swm2p interacted with Tgs1p in yeast two-hybrid screens. In the present study we show that Swm2p interacts with the N-terminus of Tgs1p and its deletion impairs pre-mRNA splicing and pre-rRNA processing. The trimethylation of spliceosomal snRNAs and the U3 snoRNA, but not other snoRNAs, was abolished in the absence of Swm2p, indicating that Swm2p is required for a substrate-specific activity of Tgs1p.


Subject(s)
Carrier Proteins/metabolism , Gene Deletion , Methyltransferases/metabolism , RNA, Small Nuclear/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/enzymology , Cell Nucleolus/metabolism , Methylation , Methyltransferases/chemistry , Protein Binding , RNA 3' End Processing/genetics , RNA Precursors/genetics , RNA Splicing/genetics , RNA, Small Nucleolar/metabolism , Ribosome Subunits, Small, Eukaryotic/metabolism , Saccharomyces cerevisiae/cytology , Substrate Specificity
9.
Hum Mol Genet ; 18(19): 3615-25, 2009 Oct 01.
Article in English | MEDLINE | ID: mdl-19592581

ABSTRACT

Spinal muscular atrophy (SMA), a recessive genetic disease, affects lower motoneurons leading to denervation, atrophy, paralysis and in severe cases death. Reduced levels of survival motor neuron (SMN) protein cause SMA. As a first step towards generating a genetic model of SMA in zebrafish, we identified three smn mutations. Two of these alleles, smnY262stop and smnL265stop, were stop mutations that resulted in exon 7 truncation, whereas the third, smnG264D, was a missense mutation corresponding to an amino acid altered in human SMA patients. Smn protein levels were low/undetectable in homozygous mutants consistent with unstable protein products. Homozygous mutants from all three alleles were smaller and survived on the basis of maternal Smn dying during the second week of larval development. Analysis of the neuromuscular system in these mutants revealed a decrease in the synaptic vesicle protein, SV2. However, two other synaptic vesicle proteins, synaptotagmin and synaptophysin were unaffected. To address whether the SV2 decrease was due specifically to Smn in motoneurons, we tested whether expressing human SMN protein exclusively in motoneurons in smn mutants could rescue the phenotype. For this, we generated a transgenic zebrafish line with human SMN driven by the motoneuron-specific zebrafish hb9 promoter and then generated smn mutant lines carrying this transgene. We found that introducing human SMN specifically into motoneurons rescued the SV2 decrease observed in smn mutants. Our analysis indicates the requirement for Smn in motoneurons to maintain SV2 in presynaptic terminals indicating that Smn, either directly or indirectly, plays a role in presynaptic integrity.


Subject(s)
Motor Neurons/metabolism , Muscular Atrophy, Spinal/metabolism , Mutation , Neuromuscular Junction/metabolism , Survival of Motor Neuron 1 Protein/metabolism , Zebrafish/metabolism , Amino Acid Sequence , Animals , Disease Models, Animal , Humans , Molecular Sequence Data , Muscular Atrophy, Spinal/genetics , Neuromuscular Junction/genetics , Sequence Alignment , Survival of Motor Neuron 1 Protein/genetics , Synaptic Vesicles/genetics , Synaptic Vesicles/metabolism , Zebrafish/genetics , Zebrafish/growth & development
10.
Dev Neurobiol ; 68(2): 182-94, 2008 Feb 01.
Article in English | MEDLINE | ID: mdl-18000835

ABSTRACT

A paramount question in spinal muscular atrophy (SMA) research is why reduced levels of SMN, a ubiquitously expressed protein, leads to a motoneuron-specific disease. It has been hypothesized that SMN may have a dual function: a role in snRNP assembly and a novel function that affects axons. We have previously shown that decreasing Smn levels in zebrafish causes defects in motor axon outgrowth. To determine whether decreasing other components of the snRNP complex would also cause motor axon defects, we knocked down Gemin2, a SMN binding protein involved in snRNP assembly. Moderate knockdown of Gemin2 yields a large percentage of morphologically abnormal embryos with shortened trunks and overall delayed development. Examination of motor axons revealed that only embryos with abnormal body morphology had aberrant motor axons indicating that the motor axon defects are secondary to the overall body defects observed in these embryos. To directly test this, we knocked down Gemin2 specifically in motoneurons using two separate approaches and found that motor axons developed normally. Furthermore, wild-type neurons transplanted into morphologically abnormal gemin2 morphants had aberrant motor axons indicating that the motor axon defects observed when Gemin2 is decreased are secondary to the defects in body morphology. These data show that reduction of Gemin2, unlike reduction of SMN, in zebrafish embryos does not directly cause motor axon outgrowth defects. Since Gemin2 and SMN both function in snRNP biogenesis yet only SMN knockdown causes motor axon defects, these data are consistent with an additional role for SMN that is snRNP independent.


Subject(s)
Carrier Proteins/metabolism , Cyclic AMP Response Element-Binding Protein/metabolism , Growth Cones/metabolism , Motor Neurons/metabolism , Nerve Tissue Proteins/metabolism , RNA-Binding Proteins/metabolism , Zebrafish Proteins/metabolism , Zebrafish/embryology , Zebrafish/metabolism , Animals , Carrier Proteins/genetics , Cell Differentiation/genetics , Down-Regulation/genetics , Embryonic Development/physiology , Gene Expression Regulation, Developmental/genetics , Growth Cones/ultrastructure , Intracellular Signaling Peptides and Proteins , Motor Neurons/cytology , Muscle, Skeletal/growth & development , Muscle, Skeletal/innervation , RNA Interference , Ribonucleoproteins, Small Nuclear/genetics , Ribonucleoproteins, Small Nuclear/metabolism , SMN Complex Proteins , Survival of Motor Neuron 1 Protein , Zebrafish Proteins/genetics
11.
Nat Struct Mol Biol ; 14(11): 1077-83, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17934474

ABSTRACT

Prp8 protein (Prp8p) is a highly conserved pre-mRNA splicing factor and a component of spliceosomal U5 small nuclear ribonucleoproteins (snRNPs). Although it is ubiquitously expressed, mutations in the C terminus of human Prp8p cause the retina-specific disease retinitis pigmentosa (RP). The biogenesis of U5 snRNPs is poorly characterized. We present evidence for a cytoplasmic precursor U5 snRNP in yeast that lacks the mature U5 snRNP component Brr2p and depends on a nuclear localization signal in Prp8p for its efficient nuclear import. The association of Brr2p with the U5 snRNP occurs within the nucleus. RP mutations in Prp8p in yeast result in nuclear accumulation of the precursor U5 snRNP, apparently as a consequence of disrupting the interaction of Prp8p with Brr2p. We therefore propose a novel assembly pathway for U5 snRNP complexes that is disrupted by mutations that cause human RP.


Subject(s)
Ribonucleoprotein, U5 Small Nuclear/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Humans , In Situ Hybridization , Macromolecular Substances/metabolism , Mutation , Nuclear Localization Signals , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , RNA Helicases , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Repressor Proteins/genetics , Repressor Proteins/metabolism , Retinitis Pigmentosa/metabolism , Ribonucleoprotein, U4-U6 Small Nuclear , Ribonucleoprotein, U5 Small Nuclear/genetics , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/chemistry , Saccharomyces cerevisiae Proteins/genetics
12.
Nucleic Acids Res ; 35(3): 923-9, 2007.
Article in English | MEDLINE | ID: mdl-17251193

ABSTRACT

Lsm proteins are ubiquitous, multifunctional proteins that are involved in the processing and/or turnover of many, if not all, RNAs in eukaryotes. They generally interact only transiently with their substrate RNAs, in keeping with their likely roles as RNA chaperones. The spliceosomal U6 snRNA is an exception, being stably associated with the Lsm2-8 complex. The U6 snRNA is generally considered to be intrinsically nuclear but the mechanism of its nuclear retention has not been demonstrated, although La protein has been implicated. We show here that the complete Lsm2-8 complex is required for nuclear accumulation of U6 snRNA in yeast. Therefore, just as Sm proteins effect nuclear localization of the other spliceosomal snRNPs, the Lsm proteins mediate U6 snRNP localization except that nuclear retention is the likely mechanism for the U6 snRNP. La protein, which binds only transiently to the nascent U6 transcript, has a smaller, apparently indirect, effect on U6 localization that is compatible with its proposed role as a chaperone in facilitating U6 snRNP assembly.


Subject(s)
Cell Nucleus/chemistry , RNA, Small Nuclear/analysis , Ribonucleoproteins, Small Nuclear/physiology , Saccharomyces cerevisiae Proteins/physiology , Cell Nucleus/metabolism , Gene Deletion , RNA Caps/physiology , RNA, Small Nuclear/chemistry , RNA, Small Nuclear/metabolism , RNA-Binding Proteins/physiology , Ribonucleoproteins, Small Nuclear/analysis , Ribonucleoproteins, Small Nuclear/genetics , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/analysis , Saccharomyces cerevisiae Proteins/genetics , Spliceosomes/metabolism , beta Karyopherins/metabolism
13.
Mol Cell Biol ; 26(16): 6016-23, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16880513

ABSTRACT

The Ntr1 and Ntr2 proteins of Saccharomyces cerevisiae have been reported to interact with proteins involved in pre-mRNA splicing, but their roles in the splicing process are unknown. We show here that they associate with a postsplicing complex containing the excised intron and the spliceosomal U2, U5, and U6 snRNAs, supporting a link with a late stage in the pre-mRNA splicing process. Extract from cells that had been metabolically depleted of Ntr1 has low splicing activity and accumulates the excised intron. Also, the level of U4/U6 di-snRNP is increased but those of the free U5 and U6 snRNPs are decreased in Ntr1-depleted extract, and increased levels of U2 and decreased levels of U4 are found associated with the U5 snRNP protein Prp8. These results suggest a requirement for Ntr1 for turnover of the excised intron complex and recycling of snRNPs. Ntr1 interacts directly or indirectly with the intron release factor Prp43 and is required for its association with the excised intron. We propose that Ntr1 promotes release of excised introns from splicing complexes by acting as a spliceosome receptor or RNA-targeting factor for Prp43, possibly assisted by the Ntr2 protein.


Subject(s)
RNA Helicases/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Spliceosomes/metabolism , DEAD-box RNA Helicases , Introns/genetics , Protein Binding , RNA Splicing/genetics , Ribonucleoproteins, Small Nuclear/metabolism , Saccharomyces cerevisiae/genetics
14.
RNA ; 12(2): 198-205, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16373487

ABSTRACT

We describe a novel approach to characterize the functional domains of a protein in vivo. This involves the use of a custom-built Tn5-based transposon that causes the expression of a target gene as two contiguous polypeptides. When used as a genetic screen to dissect the budding yeast PRP8 gene, this showed that Prp8 protein could be dissected into three distinct pairs of functional polypeptides. Thus, four functional domains can be defined in the 2413-residue Prp8 protein, with boundaries in the regions of amino acids 394-443, 770, and 2170-2179. The central region of the protein was resistant to dissection by this approach, suggesting that it represents one large functional unit. The dissected constructs allowed investigation of factors that associate strongly with the N- or the C-terminal Prp8 protein fragments. Thus, the U5 snRNP protein Snu114p associates with Prp8p in the region 437-770, whereas fragmenting Prp8p at residue 2173 destabilizes its association with Aar2p.


Subject(s)
Saccharomyces cerevisiae Proteins/chemistry , Saccharomyces cerevisiae Proteins/metabolism , Base Sequence , Binding Sites , DNA Transposable Elements , Molecular Sequence Data , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , Protein Engineering/methods , Protein Interaction Mapping , Protein Structure, Tertiary , Recombinant Proteins/genetics , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Ribonucleoprotein, U4-U6 Small Nuclear , Ribonucleoprotein, U5 Small Nuclear , Saccharomyces cerevisiae Proteins/genetics , Saccharomyces cerevisiae Proteins/isolation & purification
15.
Biomaterials ; 24(13): 2405-12, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12699678

ABSTRACT

Prolonged delivery of neurotrophic proteins to the target tissue is valuable in the treatment of various disorders of the nervous system. We have tested in this study whether sustained release of nerve growth factor (NGF) within nerve guide conduits (NGCs), a device used to repair injured nerves, would augment peripheral nerve regeneration. NGF-containing polymeric microspheres fabricated from a biodegradable poly(phosphoester) (PPE) polymer were loaded into silicone or PPE conduits to provide for prolonged, site-specific delivery of NGF. The conduits were used to bridge a 10 mm gap in a rat sciatic nerve model. Three months after implantation, morphological analysis revealed higher values of fiber diameter, fiber population and fiber density and lower G-ratio at the distal end of regenerated nerve cables collected from NGF microsphere-loaded silicone conduits, as compared with those from control conduits loaded with either saline alone, BSA microspheres, or NGF protein without microencapsulation. Beneficial effects on fiber diameter, G-ratio and fiber density were also observed in the permeable PPE NGCs. Thus, the results confirm a long-term promoting effect of exogenous NGF on morphological regeneration of peripheral nerves. The tissue-engineering approach reported in this study of incorporation of a microsphere protein release system into NGCs holds potential for improved functional recovery in patients whose injured nerves are reconstructed by entubulation.


Subject(s)
Absorbable Implants , Drug Implants/administration & dosage , Nanotechnology/methods , Nerve Growth Factor/administration & dosage , Nerve Regeneration/drug effects , Sciatic Nerve/drug effects , Sciatic Nerve/physiology , Animals , Coated Materials, Biocompatible/chemical synthesis , Drug Implants/chemical synthesis , Male , Materials Testing , Microspheres , Nanotechnology/instrumentation , Nerve Regeneration/physiology , Particle Size , Peripheral Nerves/cytology , Peripheral Nerves/drug effects , Peripheral Nerves/physiology , Rats , Rats, Wistar , Sciatic Nerve/cytology
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