Identifying genetic code reassignments in nucleotide sequence databases
Identifying genetic code reassignments in nucleotide sequence databases
批准号:
9907623
负责人:
Yekaterina Shulgina
金额:
$3.22万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-12-16 至 2021-12-15
关键词:
AccidentsAddressAmino Acid SequenceAmino Acid Sequence DatabasesAmino AcidsBase SequenceBiologicalCandida albicansChargeCodon NucleotidesCommunicationComputer AnalysisComputing MethodologiesDNADNA SequenceDataData SetDevelopmentEnsureEnvironmentEvolutionFreezingGenbankGenesGenetic CodeGenetic ModelsGenetic VariationGenomeHomologous ProteinHumanLaboratoriesLifeMass Spectrum AnalysisMetagenomicsMethodsMitochondriaModernizationMycoplasma pneumoniaeNatureNorthern BlottingOralOrganismPeptide Sequence DeterminationProcessProteinsProteomeProteomicsResearch PersonnelResearch TrainingScienceTertiary Protein StructureTestingTrainingTransfer RNATransfer RNA AminoacylationTranslatingTranslationsTreesUpdateWritingYeastscareercomparativecomputerized toolscontigexperimental studyfollow-upgenetic predictorsgenetic variantgenome annotationin silicolaboratory equipmentmolecular sequence databasenovelopen sourcepathogenic bacteriapressureprogramsskills
中文摘要
项目摘要
在其他生物体中的生物学发现告诉我们人类的功能
基因,因为能够比较同源蛋白质序列。最近努力
序列更大的物种多样性进行比较分析,主要是在
DNA水平和蛋白质序列随后在计算机上翻译,假设一些
遗传密码然而,目前还没有选择正确的遗传密码的知情方法
对于新测序的生物体,这对于预测蛋白质的正确翻译至关重要
序列的随着越来越多的生物体被测序,使用变异遗传密码的物种
继续被发现,这表明可能有一个隐藏的替代遗传多样性,
生命之树上的密码
目的1提出建立一个计算工具来预测遗传密码所使用的
单从核苷酸序列来看。这将填补基因组中关键的缺失步骤,
注释管道,并将确保蛋白质序列数据库的准确性,
主要由预测的蛋白质序列组成。在目标2中,计算工具将
用于推断所有公开可用的基因组的遗传密码使用,并验证任何新的
通过计算分析tRNA基因的遗传密码,实验证实tRNA
通过北方印迹表达,并通过蛋白质组学证实改变的密码子翻译
质谱分析法来在目标3中,将使用替代遗传密码的最新分布
解决该领域长期存在的关于遗传密码如何被认为是
进化
本研究培训计划旨在为PI作为独立研究员的职业生涯做好准备。
跨学科研究者。培训环境将是一个合作的环境。
计算实验室,可以使用实验台和共享实验室设备来完成
提出的实验。培训计划还将包括发展科学
沟通技巧,包括口头报告和写作。
英文摘要
Project Summary Abstract
Biological discoveries made in other organisms tell us about the functions of human
genes because of the ability to compare homologous protein sequences. Recent efforts to
sequence a greater diversity of species for comparative analysis have been primarily done on
the DNA level, and protein sequences are subsequently translated in silico assuming some
genetic code. However, there is currently no informed way of selecting the correct genetic code
for a newly sequenced organism, which is critical for the correct translation of predicted protein
sequences. As more diverse organisms are sequenced, species using variant genetic codes
continue to be found, suggesting that there may be a hidden diversity of alternative genetic
codes across the tree of life.
Aim 1 proposes building a computational tool to predict the genetic code used by an
organism from nucleotide sequence alone. This would fill in a critical missing step in genome
annotation pipelines and would ensure the accuracy of protein sequence databases, which are
predominantly composed of predicted protein sequences. In aim 2, the computational tool will
be used to infer the genetic code usage of all publicly available genomes and validate any new
genetic codes by computational analysis of tRNA genes, experimental confirmation of tRNA
expression via Northern blotting, and confirmation of altered codon translation via proteomic
mass spectrometry. In aim 3, the updated distribution of alternative genetic codes will be used
to address long-standing hypotheses in the field about how the genetic code is thought to
evolve.
This research training plan is intended to prepare the PI for a career as an independent
and interdisciplinary researcher. The training environment will be in a collaborative
computational laboratory, with access to a lab bench and shared lab equipment to do the
proposed experiments. The training plan will also include development of science
communication skills, including oral presentations and writing.
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