R35GM158209
Project Grant
Overview
Grant Description
DECODING POSITIONAL EPIGENETIC MEMORY - PROJECT SUMMARY / ABSTRACT: DECODING POSITIONAL EPIGENETIC MEMORY HOX GENE EXPRESSION IS CRUCIAL FOR PATTERNING THE MAIN BODY AXIS OF ALL BILATERIAN SPECIES. IN A CLASSIC EPIGENETIC MEMORY FASHION, POSITIONAL IDENTITY IS ACQUIRED EARLY IN DEVELOPMENT AND IS INHERITED THROUGH CELL LINEAGE VIA HOX EXPRESSION. MISEXPRESSION OF EVEN A SINGLE HOX GENE CAN LEAD TO HOMEOTIC TRANSFORMATIONS OR DISEASES LIKE CANCER, MAKING STABLE AND ACCURATE HOX POSITIONAL EPIGENETIC MEMORY ESSENTIAL FOR PROPER CELL DIFFERENTIATION AND DISEASE PREVENTION. BUILDING ON A DECADE OF SEMINAL CONTRIBUTIONS TO THE FIELD, OUR RESEARCH AIMS TO DECIPHER HOW STABLE HOX POSITIONAL IDENTITY IS GENERATED. IN MAMMALS, THE HOX GENES ARE ORGANIZED INTO FOUR CHROMOSOMAL CLUSTERS, EACH CONTAINING A SUBSET OF 13 GENES WITHIN APPROXIMATELY 100 KB. POLYCOMB REPRESSIVE COMPLEXES (PRCS) DECORATE AND SUPPRESS HOX CLUSTERS IN UNDIFFERENTIATED CELLS. TRANSIENT PATTERNING SIGNALS SUCH AS RETINOIC ACID PARTITION HOX CLUSTERS INTO ACTIVE (PRC-REMOVED) AND REPRESSED (PRC-HIGH) DOMAINS AT EARLY DIFFERENTIATION STAGES, ESTABLISHING PRECISE AND STABLE BOUNDARIES THAT CONVEY POSITIONAL IDENTITY ACROSS CELL GENERATIONS. WE MADE THREE CRITICAL CONTRIBUTIONS TO THE ACCEPTED HOX POSITIONAL EPIGENETIC MEMORY MODEL. FIRST, WE IDENTIFIED THAT PATTERNING SIGNALS RESULT IN THE BINDING OF ACTIVATING TRANSCRIPTION FACTORS TO HOX CLUSTER DOMAINS. SECOND, WE DISCOVERED THAT THIS BINDING RESULTS IN PRC EVICTION FROM CTCF-ESTABLISHED CHROMATIN BOUNDARIES. LASTLY, WE DEMONSTRATED THAT THE HOX CLUSTER IS SUFFICIENT TO ESTABLISH POSITIONAL IDENTITY. IN OTHER WORDS, A 100 KB HOX CLUSTER ENGAGES WITH THE THREE ELEMENTS REQUIRED FOR POSITIONAL MEMORY: REPRESSION (PRC RECRUITMENT), ACTIVATION (SIGNALING TRANSCRIPTION FACTORS), AND BOUNDARY FORMATION (CTCF). THE ABILITY OF CTCF TO ENGAGE IN BOUNDARY FORMATION IS AN ACTIVE AREA OF RESEARCH AND THE BEST-UNDERSTOOD COMPONENT. HOWEVER, THERE IS A KNOWLEDGE GAP IN THE MECHANISMS THAT CONTROL ACTIVATION AND REPRESSION: CHALLENGE 1: ACTIVATION. THE CURRENT WORKING MODEL CANNOT EXPLAIN HOW RETINOIC ACID SIGNALING EVICTS PRC WHILE INITIATING A PROGRESSIVE COLINEAR HOX GENE TRANSCRIPTION. FURTHER, THE MODEL LACKS DEFINITIVE PROOF OF THE PHYSICAL DISTRIBUTION OF THE ACTIVATING RETINOIC ACID RECEPTOR AND CDX2 FACTORS ALONG HOX CLUSTER DOMAINS. WE WILL CHALLENGE THE HOX REGULATORY PARADIGM TO THE CORE BY BUILDING NOVEL HOX REGULATORY UNITS WITH SYNTHETIC DNA TECHNOLOGY. CHALLENGE 2: REPRESSORS. ALTHOUGH IT IS AMONG THE EARLIEST EXAMPLES OF PRC REPRESSION, THERE IS NO MECHANISTIC UNDERSTANDING OF HOW HOX CLUSTERS RECRUIT PRC IN MAMMALIAN CELLS. WITH OUR POWERFUL SYNTHETIC DNA APPROACH, WE WILL IDENTIFY THE MAMMALIAN HOX POLYCOMB RECRUITMENT ELEMENT (PRE). BY MERGING SYNTHETIC DNA, NEW GENOMIC ENGINEERING TOOLS, AND STEM CELL DIFFERENTIATION SYSTEMS, WE AIM TO UNDERSTAND POSITIONAL MEMORY THROUGH HOX CHROMATIN BOUNDARY FORMATION AND BUILD THE SMALLEST GENETIC UNIT SUFFICIENT TO ESTABLISH AND SUSTAIN POSITIONAL EPIGENETIC MEMORY.
Awardee
Funding Goals
THE NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES (NIGMS) SUPPORTS BASIC RESEARCH THAT INCREASES OUR UNDERSTANDING OF BIOLOGICAL PROCESSES AND LAYS THE FOUNDATION FOR ADVANCES IN DISEASE DIAGNOSIS, TREATMENT, AND PREVENTION. NIGMS ALSO SUPPORTS RESEARCH IN SPECIFIC CLINICAL AREAS THAT AFFECT MULTIPLE ORGAN SYSTEMS: ANESTHESIOLOGY AND PERI-OPERATIVE PAIN, CLINICAL PHARMACOLOGY ?COMMON TO MULTIPLE DRUGS AND TREATMENTS, AND INJURY, CRITICAL ILLNESS, SEPSIS, AND WOUND HEALING.? NIGMS-FUNDED SCIENTISTS INVESTIGATE HOW LIVING SYSTEMS WORK AT A RANGE OF LEVELSFROM MOLECULES AND CELLS TO TISSUES AND ORGANSIN RESEARCH ORGANISMS, HUMANS, AND POPULATIONS. ADDITIONALLY, TO ENSURE THE VITALITY AND CONTINUED PRODUCTIVITY OF THE RESEARCH ENTERPRISE, NIGMS PROVIDES LEADERSHIP IN SUPPORTING THE TRAINING OF THE NEXT GENERATION OF SCIENTISTS, ENHANCING THE DIVERSITY OF THE SCIENTIFIC WORKFORCE, AND DEVELOPING RESEARCH CAPACITY THROUGHOUT THE COUNTRY.
Grant Program (CFDA)
Place of Performance
New York
United States
Geographic Scope
State-Wide
New York University was awarded
Deciphering Stable HOX Positional Epigenetic Memory
Project Grant R35GM158209
worth $3,125,817
from the HHS Office of the Assistant Secretary for Financial Resources in August 2025 with work to be completed primarily in New York United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.859 Biomedical Research and Research Training.
The Project Grant was awarded through grant opportunity Maximizing Investigators' Research Award (R35 - Clinical Trial Optional).
Status
(Ongoing)
Last Modified 8/20/25
Period of Performance
8/5/25
Start Date
7/31/29
End Date
Funding Split
$3.1M
Federal Obligation
$0.0
Non-Federal Obligation
$3.1M
Total Obligated
Activity Timeline
Additional Detail
Award ID FAIN
R35GM158209
SAI Number
R35GM158209-4179408443
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NS00 NIH National Institute of General Medical Sciences
Funding Office
75AM00 ASFR OFFICE OF THE ASSISTANT SECRETARY FOR FINANCIAL RESOURCES
Awardee UEI
M5SZJ6VHUHN8
Awardee CAGE
3D476
Performance District
NY-90
Senators
Kirsten Gillibrand
Charles Schumer
Charles Schumer
Modified: 8/20/25