The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
批准号:
9335368
负责人:
Joseph Anthony Piccirilli
金额:
$49.84万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-24 至 2018-08-31
关键词:
AchievementAddressAffectArchitectureBindingBinding SitesBiochemistryBiological AssayBiologyBypassCatalysisCatalytic DomainCatalytic RNACellsChemicalsChemistryCollaborationsCrystallizationDefectDimensionsDiseaseDockingEnzymesEukaryotaEvolutionGene ExpressionGenesGenetic TranscriptionGoalsHumanIndividualIntronsInvestigationIonsMediatingMetalsModelingMolecular GeneticsMutationNuclearPathway interactionsPlayPositioning AttributeProteinsProteomeRNARNA SplicingRegulationResolutionRoleSiteSmall Nuclear RNASpliceosomesStructureSystemTestingTranslationsWorkbasecatalystdivalent metalendonucleasehuman diseaseinorganic phosphateinsightmRNA Precursornovelpublic health relevancereconstitutionscaffoldtreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Our long-term goal is to elucidate the mechanisms by which the spliceosome catalyzes pre-mRNA splicing and in particular to define the structural and functional role of RNA and protein in catalysis. Catalysis of pre-mRNA splicing by the spliceosome is a defining feature of eukaryotes. In humans, catalysis is required to excise ten introns on average for nearly every gene, and catalysis at alternative sites expands the proteome and contributes to the complexity of higher eukaryotes. Indeed, mutations in at least 15% of human diseases result from errors in splicing. Despite this importance of pre-mRNA splicing to eukaryotic gene expression, for decades our understanding of splicing catalysis has languished, particularly in comparison to our understanding of catalysis at the two other major stages of gene expression - transcription and translation. We have not even known whether catalysis is mediated by the RNA or protein parts of the spliceosome. However, through our collaborative efforts, we have recently provided definitive evidence that the RNA parts catalyze splicing, positioning two divalent metal ions for interaction with the scissile phosphates. Strikingly, our work also establishes that the spliceosome utilizes a catalytic mechanism indistinguishable from the catalytic mechanism of self-splicing group II RNA introns, extending the parallels with the group II intron to the atomic level at the catalytic core and providing strog support for the hypothesis that these two enzymes share common evolutionary origins. Despite this advance and other achievements in the field, many fundamental questions remain. For example, how are the nucleophiles in either splicing system activated for catalysis, how does the architecture of the spliceosomal catalytic core position the reactive sites for catalysis, and what is the role of protein in mediating RNA-based catalysis? To answer these questions, we aim to test a metal cluster model for catalysis of nuclear pre-mRNA splicing, to define the architecture and dynamics of the catalytic core of the spliceosome, and to define the essential role of protein in assisting RNA-based splicing catalysis. We will accomplish these aims through a continuation of our unique and synergistic collaboration that allows for a combined approach of chemistry, biochemistry and molecular genetics. This work will transform our understanding of the roles of RNA and protein in spliceosomal catalysis, with significant implications for understanding the origins and evolution of the spliceosome.
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A conformational switch in PRP8 mediates metal ion coordination that promotes pre-mRNA exon ligation.
PRP8中的构象开关介导了促进前MRNA外显子连接的金属离子配位。
DOI:
10.1038/nsmb.2556
发表时间:
2013-06
期刊:
NATURE STRUCTURAL & MOLECULAR BIOLOGY
影响因子:
16.8
作者:
[Schellenberg, Matthew J., Wu, Tao, Ritchie, Dustin B., Fica, Sebastian, Staley, Jonathan P., Atta, Karim A., LaPointe, Paul, MacMillan, Andrew M.]
通讯作者:
MacMillan, Andrew M.
DOI:
10.1038/nsmb.3242
发表时间:
2016-06-07
期刊:
Nature structural & molecular biology
影响因子:
16.8
作者:
[Piccirilli JA, Staley JP]
通讯作者:
Staley JP
DOI:
10.1158/0008-5472.can-16-1454
发表时间:
2017-04-01
期刊:
Cancer research
影响因子:
11.2
作者:
[Sundaram KM, Zhang Y, Mitra AK, Kouadio JK, Gwin K, Kossiakoff AA, Roman BB, Lengyel E, Piccirilli JA]
通讯作者:
Piccirilli JA
DOI:
10.1021/jo4028374
发表时间:
2014-04-18
期刊:
The Journal of organic chemistry
影响因子:
--
作者:
[Li NS, Tuttle N, Staley JP, Piccirilli JA]
通讯作者:
Piccirilli JA
Synthesis, properties, and applications of oligonucleotides containing an RNA dinucleotide phosphorothiolate linkage.
含有RNA二核苷酸磷酸硫酸酯链接的寡核苷酸的合成,性质和应用。
DOI:
10.1021/ar200131t
发表时间:
2011-12-20
期刊:
ACCOUNTS OF CHEMICAL RESEARCH
影响因子:
18.3
作者:
[Li, Nan-Sheng, Frederiksen, John K., Piccirilli, Joseph A.]
通讯作者:
Piccirilli, Joseph A.
共 6 条
Structure and Function of Non-Coding RNA
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批准号:10623993
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项目类别:
-
资助金额:$81.31万
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财政年份:2023
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负责人:Joseph Anthony Piccirilli
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依托单位:
The VS Ribozyme: Catalytic Mechanism, Transition State Structure, and Evolution
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批准号:10305610
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项目类别:
-
资助金额:$32.31万
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财政年份:2019
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负责人:Joseph Anthony Piccirilli
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依托单位:
The VS Ribozyme: Catalytic Mechanism, Transition State Structure, and Evolution
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批准号:10582360
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项目类别:
-
资助金额:$7.57万
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财政年份:2019
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负责人:Joseph Anthony Piccirilli
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依托单位:
The VS Ribozyme: Catalytic Mechanism, Transition State Structure, and Evolution
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批准号:10061618
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项目类别:
-
资助金额:$32.31万
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财政年份:2019
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负责人:Joseph Anthony Piccirilli
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依托单位:
CHAPERONE-ASSISTED RNA CRYSTALLOGRAPHY - Resubmission 01
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批准号:8506004
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项目类别:
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资助金额:$33.13万
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财政年份:2013
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负责人:Joseph Anthony Piccirilli
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依托单位:
Chaperone-Assisted RNA Crystallography
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批准号:10058842
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项目类别:
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资助金额:$38.04万
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财政年份:2013
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负责人:Joseph Anthony Piccirilli
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依托单位:
CHAPERONE-ASSISTED RNA CRYSTALLOGRAPHY - Resubmission 01
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批准号:9037690
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项目类别:
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资助金额:$32.37万
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财政年份:2013
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负责人:Joseph Anthony Piccirilli
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依托单位:
CHAPERONE-ASSISTED RNA CRYSTALLOGRAPHY - Resubmission 01
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批准号:8643797
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项目类别:
-
资助金额:$32.37万
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财政年份:2013
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负责人:Joseph Anthony Piccirilli
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依托单位:
Chaperone-Assisted RNA Crystallography-Equipment Supplement
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批准号:9895189
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项目类别:
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资助金额:$8.6万
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财政年份:2013
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:8788330
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项目类别:
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资助金额:$54.09万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
Investigating the Catalytic Mechanism of the HDV Ribozyme
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批准号:8465171
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项目类别:
-
资助金额:$35.29万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
Investigating the Catalytic Mechanism of the HDV Ribozyme
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批准号:8663828
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项目类别:
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资助金额:$37.55万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
Investigating the Catalytic Mechanism of the HDV Ribozyme
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批准号:8074914
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项目类别:
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资助金额:$37.55万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
Investigating the Catalytic Mechanism of the HDV Ribozyme
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批准号:7785036
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项目类别:
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资助金额:$28.44万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
Investigating the Catalytic Mechanism of the HDV Ribozyme
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批准号:8277979
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项目类别:
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资助金额:$37.55万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:8324223
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项目类别:
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资助金额:$49.06万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:9276215
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项目类别:
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资助金额:$22.53万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:8912481
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项目类别:
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资助金额:$49.84万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:8535166
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项目类别:
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资助金额:$47.36万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
The Catalytic Mechanism of Nuclear Premessenger RNA Splicing by the Spliceosome
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批准号:8147769
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项目类别:
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资助金额:$48.37万
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财政年份:2010
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负责人:Joseph Anthony Piccirilli
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依托单位:
海外基金