Molecular mechanisms of mammalian circadian clock function
哺乳动物生物钟功能的分子机制
基本信息
- 批准号:9980934
- 负责人:
- 金额:$ 65.8万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-08-07 至 2023-07-31
- 项目状态:已结题
- 来源:
- 关键词:ARNTL geneAutomobile DrivingBehaviorBiochemistryCardiovascular DiseasesCell physiologyCholesterol HomeostasisCircadian DysregulationCircadian RhythmsClock proteinCrystallizationCytosolDataDiabetes MellitusDietExhibitsExpression ProfilingFeedbackFutureGene ExpressionGenesGeneticGenetic TranscriptionHealthHumanJet Lag SyndromeLengthLinkLiverMalignant NeoplasmsMammalsMediator of activation proteinMental disordersMessenger RNAMetabolicMitochondriaModalityModelingMolecularMusObesityPeriodicityPhysiologyPoly(A) TailPolyadenylationPost-Transcriptional RegulationProteinsRegulationResistanceRoleStructureSystemTailTimeTranslational RegulationTriglyceride MetabolismWorkcircadiancircadian pacemakercomplex data cryptochrome 1cryptochrome 2insightnocturninprotein expressionshift worktranscription factor
项目摘要
Abstract
Circadian clocks throughout the body drive rhythmic expression of thousands of genes, resulting in
rhythms in biochemistry, physiology and behavior. Disruption of circadian clocks through genetics or
environmental perturbations such as jet lag or shift-work, can have profound negative consequences
and has been linked to obesity, diabetes, cancer, cardiovascular disease and mental illness. Our
work is focused generally on understanding the detailed molecular mechanisms of the mammalian
circadian clock machinery and the mechanisms by which these clocks control rhythmic gene
expression. According to the current model, the core part of this clock mechanism is a negative
feedback loop whereby the transcription factor heterodimer CLOCK/BMAL1 drives transcription of the
“clock” proteins PERIOD (PER) 1, PER 2, CRYPTOCHROME (CRY) 1 and CRY 2 which interact with
each other to repress the activity of CLOCK/BMAL1, and thus their own synthesis. We have solved
crystal structures for the CLOCK/BMAL1 and CRY2/PER2 complexes and these data have allowed
the identification of evolutionarily conserved functional domains throughout the proteins and revealed
additional insights into the mechanisms by which these proteins operate and set the circadian period.
Over the next five years, we will expand on this information to determine the atomic details of how
this clock keeps time. The roles of these core circadian clock transcription factors in driving rhythmic
transcription is well-documented, but recent data have demonstrated that post-transcriptional control,
although much less well understood, is also critical for normal rhythmic protein expression profiles.
One type of post-transcriptional control is regulation of mRNA poly(A) tail length, which impacts the
stability and translational regulation of mRNA. We have identified hundreds of mouse liver mRNAs
that exhibit robust circadian rhythms in the length of their poly(A) tails. In many of these cases, the
rhythmic tail lengths are the result of rhythmic cytoplasmic polyadenylation and deadenylation
rhythms and many components of the cytoplasmic polyadenylation and deadenylation machinery are
themselves under circadian control. Furthermore, the rhythmic poly(A) tails are closely correlated
with the rhythmic protein expression. Therefore, the circadian clock regulates dynamic
polyadenylation status of many mRNAs that can drive rhythmic protein expression independent of the
steady-state levels of the message. Nocturnin is a robustly rhythmic protein that removes poly(A) tails
from mRNAs. We have shown that loss of this gene in mice causes resistance to diet-induced
obesity and altered rhythms in cholesterol and triglyceride metabolism, implicating it as an important
circadian post-transcriptional mediator. Over the next five years, we will focus on identifying the
mRNA substrates of Nocturnin both in the cytosol and in the mitochondria.
摘要
项目成果
期刊论文数量(0)
专著数量(0)
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Carla B. Green其他文献
Cryptochromes
- DOI:
10.1016/j.cub.2005.09.030 - 发表时间:
2005-10-11 - 期刊:
- 影响因子:
- 作者:
Ellena van der Schalie;Carla B. Green - 通讯作者:
Carla B. Green
Carla B. Green的其他文献
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{{ truncateString('Carla B. Green', 18)}}的其他基金
Role of the circadian protein Nocturnin in modulating oxidative stress in substantia nigra dopaminergic neurons
昼夜节律蛋白Nocturnin在调节黑质多巴胺能神经元氧化应激中的作用
- 批准号:
10066683 - 财政年份:2020
- 资助金额:
$ 65.8万 - 项目类别:
Molecular mechanisms of mammalian circadian clock function
哺乳动物生物钟功能的分子机制
- 批准号:
10458088 - 财政年份:2018
- 资助金额:
$ 65.8万 - 项目类别:
Molecular mechanisms of mammalian circadian clock function
哺乳动物生物钟功能的分子机制
- 批准号:
10225593 - 财政年份:2018
- 资助金额:
$ 65.8万 - 项目类别:
Molecular mechanisms of mammalian circadian clock function
哺乳动物生物钟功能的分子机制
- 批准号:
9757788 - 财政年份:2018
- 资助金额:
$ 65.8万 - 项目类别:
Molecular mechanisms of mammalian circadian clock function
哺乳动物生物钟功能的分子机制
- 批准号:
10455876 - 财政年份:2018
- 资助金额:
$ 65.8万 - 项目类别:
Molecular mechanisms of mammalian circadian clock function - Renewal - 1
哺乳动物生物钟功能的分子机制 - 更新 - 1
- 批准号:
10623521 - 财政年份:2018
- 资助金额:
$ 65.8万 - 项目类别:
Circadian dynamics of cytoplasmic mRNA polyadenylation and deadenylation
细胞质 mRNA 多腺苷酸化和去腺苷酸化的昼夜动态
- 批准号:
9213380 - 财政年份:2016
- 资助金额:
$ 65.8万 - 项目类别:
Circadian dynamics of cytoplasmic mRNA polyadenylation and deadenylation
细胞质 mRNA 多腺苷酸化和去腺苷酸化的昼夜动态
- 批准号:
9026882 - 财政年份:2016
- 资助金额:
$ 65.8万 - 项目类别:
Circadian regulation of mitochondrial RNA polyadenylation
线粒体 RNA 多腺苷酸化的昼夜节律调节
- 批准号:
8747363 - 财政年份:2014
- 资助金额:
$ 65.8万 - 项目类别:
Circadian regulation of mitochondrial RNA polyadenylation
线粒体 RNA 多腺苷酸化的昼夜节律调节
- 批准号:
9090194 - 财政年份:2014
- 资助金额:
$ 65.8万 - 项目类别:
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