Potential Role of Compass H3K4 Methyltransferase Complexes in Environmental Circadian-Alignment
Project Number5R16GM146703-03
Contact PI/Project LeaderDUONG, HAO
Awardee OrganizationMOREHOUSE SCHOOL OF MEDICINE
Description
Abstract Text
Summary/Abstract
Environmental-Circadian Disruption such as shiftwork and Jetlag imposes major risk on
human health in the U.S. and abroad. It increases the risk of many metabolic and cardiovascular
disorders and cancers and effects over 16% of the U.S. workforce. Yet, the molecular
underpinnings of this process remain unclear.
In a proteomic analysis of proteins interacting with Cry1, we identified 10 components of
COMPASS complexes. These enzymatic complexes regulate gene transcription by catalyzing
the addition of methyl groups to lysine 4 of histone 3 (H3K4mes) of local chromatin. Interestingly,
these chromatin marks respond to environmental circadian entrainment information such as
light, temperature or nutrients. They also happen in a circadian rhythmic manner and modulate
DNA methylation, a determinant of gene transcription and disease development. Furthermore,
functional perturbations of various COMPASS components were also implicated in pathological
conditions associated with disharmony of environmental and circadian cycles such as breast
cancer and obesity. We thus hypothesize that COMPASS complexes play a key role in
environmental-circadian alignment. Under environmental-circadian alignment condition,
COMPASS complexes are recruited by Cry1 to rhythmically methylate local H3K4s, which prevent
recruitment of DNA methyltransferases resulting in perturbations of DNA methylation and
expression of core clock gene(s). This methylation cascade modulates the circadian pattern of
gene expression, ensuring alignment of the circadian system with daily environmental cycles. The
methylation cascade fails to initiate when internal circadian system mis-aligns with external
environmental cycles, leading to perturbation of the homeostatic state of cells and development
of disorders. We will investigate this hypothesis by pursuing the following initial aims: 1: To
characterize circadian Cry1::COMPASS interaction; Aim 2: To investigate the role of COMPASS
complexes in methylation of core clock genes; Aim 3: To study the effects of environmental-
circadian disruption on COMPASS function.
The results of this project might unveil the molecular mechanism of a fundamental biological
process: synchronization of daily internal physiological rhythms with external environmental cycles.
They might also illuminate the nuts and bolts of disorders associated with shiftwork.
Public Health Relevance Statement
Narrative
This project aims to decipher potential role of a class of histone methyltransferases,
COMPASS H3K4 methyltransferases, in environmental-circadian alignment. If successful, the
results will unveil the molecular mechanism of a fundamental biological process, i.e. how
organisms synchronize daily internal circadian rhythms with external environmental cycles. It
will also lay the foundation for therapeutic avenues for conditions associated with shiftwork, a
type of environmental circadian disruption, such as obesity and cancers.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AccelerationBiological ProcessCarcinogensCardiovascular DiseasesCellsChromatinChromatin Remodeling FactorCircadian DysregulationCircadian RhythmsCircadian gene expressionClassificationClock proteinCo-ImmunoprecipitationsComplexDNA MethylationDNA Modification MethylasesDependenceDeveloping CountriesDevelopmentDiseaseEatingEnsureFoundationsFundingGene Expression ProfileGenesGeneticGenetic TranscriptionGoalsGrantHealthHistonesHospitalsHumanIndustrializationIndustryInternational Agency for Research on CancerJet Lag SyndromeKnockout MiceLeisuresLightLysineMalignant Breast NeoplasmMalignant NeoplasmsMetabolic DiseasesMethodsMethylationMethyltransferaseModelingMolecularMolecular GeneticsMultienzyme ComplexesNutrientObesityOrganismPathologicPathway interactionsPatternPeriodicityPhysiologicalPlayPositioning AttributeProbabilityProcessProtein AnalysisProteomeProteomicsPublicationsRNA InterferenceReportingRiskRoleScheduleSleepSolidSpecificityStimulusSystemSystems IntegrationTemperatureTestingTherapeuticTimeUrbanizationWorkcareerchromatin immunoprecipitationcircadiancircadian biologycircadian pacemakerdisadvantaged backgroundexperimental studyhistone methyltransferasemethyl groupmouse geneticsmouse modelnext generationpreventrecruitshift workstatisticstraining opportunitytransmission process
No Sub Projects information available for 5R16GM146703-03
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R16GM146703-03
Patents
No Patents information available for 5R16GM146703-03
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5R16GM146703-03
Clinical Studies
No Clinical Studies information available for 5R16GM146703-03
News and More
Related News Releases
No news release information available for 5R16GM146703-03
History
No Historical information available for 5R16GM146703-03
Similar Projects
No Similar Projects information available for 5R16GM146703-03