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17,054 grants matching genome editing

GRAIN LEGUMES CONSTITUTE MAJOR SOURCES OF PLANT DIETARY PROTEIN FOR HUMAN AND FEED CONSUMPTION. CURRENTLY, GENERATING NOVEL TRAITS IN THESE CROPS IS LARGELY LIMITED TO CLASSICAL MUTAGENESIS AND GENOMICS-ASSISTED BREEDING METHODS. GENE-EDITING OFFERS GREAT POTENTIAL FOR ACCELERATING CROP IMPROVEMENT THROUGH EFFICIENT AND PRECISE GENETIC MODIFICATIONS. TWO KEY TECHNOLOGICAL BARRIERS, LACK OF EFFICIENT REAGENT DELIVERY METHODS AND POOR PLANT REGENERATION RATES, HAVE IMPEDED USE OF GENE EDITING IN THESE CROPS. AGROBACTERIUM-MEDIATED TRANSFORMATION HAS BEEN THE PREFERRED METHOD TO DELIVER GENE EDITING REAGENTS IN PLANT SPECIES, BUT HAS SHOWN LITTLE SUCCESS IN GRAIN LEGUMES DUE TO THE HOST RANGE LIMITATION AND STRONG GENOTYPE-DEPENDENCY. OUR LABORATORIES HAVE BEEN DEVELOPING DIRECT DELIVERY METHODS USING BIOLISTICS OR NANOPARTICLES TO OVERCOME THESE LIMITATIONS. EFFICIENT GENE EDITING HAS BEEN ACHIEVED BY DIRECTLY DELIVERING CRISPR/CAS9 DNA OR RIBONUCLEOPROTEINS VIA THE BIOLISTIC-BASED APPROACH. MOREOVER, WE RECENTLY DEVELOPED A NEW METHOD TO IMPROVE PLANT REGENERATION USING DEVELOPMENTAL REGULATORS (DRS), SUCH AS THE BABY BOOM (BBM) AND WUSCHEL (WUS) GENES, IN SOYBEAN. IN THIS PROPOSAL, WE AIM TO EXTEND OUR DIRECT DELIVERY AND IMPROVED PLANT REGENERATION METHODS TO TWO GRAIN LEGUMES, COMMON BEAN AND CHICKPEA. BY COMBINING THESE METHODS WITH CRISPR/CAS9 REAGENTS, WE WILL EXPAND THE USE OF GENETIC TRANSFORMATION AND GENE EDITING IN GRAIN LEGUMES.

$281,184
Regents Of The University Of Minnesota · · FY2021 · National Institute of Food and Agriculture

Functional impact, mechanistic role, and targetability of ROS1 aberrations in cancer

$281,116
Monika A Davare · Oregon Health & Science University · R01 · FY2024 · CA

Mapping endogenous protein dynamics in living cells

$280,502
Bo Huang · University Of California, San Francisco · R01 · FY2020 · GM

Mapping endogenous protein dynamics in living cells

$280,502
Bo Huang · University Of California, San Francisco · R01 · FY2021 · GM

Mapping endogenous protein dynamics in living cells

$280,502
Bo Huang · University Of California, San Francisco · R01 · FY2022 · GM

Biological Core

$280,415
Carolyn Ann Worby · University Of Kentucky · P01 · FY2016 · NS

Elucidating Mechanisms of Recognition and Excision of Damaged Bases by NEIL glycosylases

$280,388
Sheila Sue David · University Of California At Davis · R01 · FY2021 · GM

THE DEVELOPMENT OF CRISPR-CAS9 AND RELATED TECHNOLOGIES FOR EDITING MAMMALIAN CELLS AND EMBRYOS HAS RESULTED IN UNPRECEDENTED OPPORTUNITIES FOR IMPROVING LIVESTOCK GENETICS. TO TAKE FULL ADVANTAGE OF GENE EDITING TECHNOLOGIES APPLIED TO ANIMALS SUCH AS INTROGRESSION OF ALLELES FOR IMPROVED GENETIC ADVANCE MULTIPLE EDITS ON THE SAME INDIVIDUAL ARE OFTEN REQUIRED WHICH CURRENTLY CONSTITUTES A TECHNOLOGICAL BARRIER FOR FOOD ANIMAL SPECIES. WE HAVE RECENTLY BEEN ABLE TO ISOLATE AND MAINTAIN STABLE BOVINE EMBRYONIC STEM CELLS (BESC) FULFILLING AN UNMET NEED FOR LIVESTOCK SPECIES THAT HAD BEEN PURSUED FOR THE LAST 30 YEARS. WE HAVE FURTHER OPTIMIZED THE CULTURE CONDITIONS FOR BOVINE ESCS AND EXTENDED THE TECHNOLOGY TO SHEEP AND GOAT SPECIES. ESCS REPRESENT AN IDEAL PLATFORM FOR INTRODUCING MULTIPLE GENETIC MODIFICATIONS AS THEY CAN BE CULTURED INDEFINITELY MAINTAIN GENOMIC STABILITY AND ARE AMENABLE TO SCNT/CLONING FOR PRODUCING ESC-DERIVED OFFSPRING. THE GOAL OF THE PROPOSED PROJECT IS TO DEVELOP A PLATFORM FOR EFFICIENT MULTIPLEX GENOME EDITING IN CATTLE GOAT AND SHEEP. WE WILL PURSUE THE FOLLOWING SPECIFIC OBJECTIVES: 1) TO OPTIMIZE CRISPR-CAS9 DELIVERY AND GENOME EDITING REAGENTS FOR EFFICIENT GENE DISRUPTION ALLELE INTROGRESSION AND TARGETED GENE INSERTION IN BOVINE OVINE AND CAPRINE ESCS; AND 2) TO OPTIMIZE CONDITIONS FOR MULTIPLEXED GENE EDITING IN CATTLE ESCS. OUTCOMES OF THIS PROPOSAL WILL INCLUDE STEM CELL-BASED PLATFORMS FOR RAPID AND EFFICIENT INTRODUCTION OF MULTIPLE GENOMIC MODIFICATIONS IN THREE IMPORTANT FOOD ANIMAL SPECIES.

$280,056
University Of California, Davis · · FY2020 · National Institute of Food and Agriculture

A new tool for the cell-specific identification of RNA binding protein targets

$279,984
Michael Rosbash · Brandeis University · R01 · FY2016 · DA

EAGER: Generating diploid gametes in maize

$279,922
Venkatesan Sundaresan · University Of California-Davis · · FY2025 · BIO

Mitochondria mediated intercellular metabolic coupling in bone marrow regeneration

$279,840
Jose A. Cancelas · Cincinnati Childrens Hosp Med Ctr · R01 · FY2020 · DK

Mitochondria mediated intercellular metabolic coupling in bone marrow regeneration

$279,840
Jose A. Cancelas · Cincinnati Childrens Hosp Med Ctr · R01 · FY2022 · DK

Mitochondria mediated intercellular metabolic coupling in bone marrow regeneration

$279,840
Jose A. Cancelas · Cincinnati Childrens Hosp Med Ctr · R01 · FY2021 · DK

Understanding the Healthy Gut Virome and its Role in Human Health

$279,780
Mark J Young · Montana State University - Bozeman · R01 · FY2016 · GM

Cancer Center Administration

$279,704
David M Gosky · Ohio State University · P30 · FY2024 · CA

Cancer Center Administration

$279,702
David M Gosky · Ohio State University · P30 · FY2023 · CA

Cancer Center Administration

$279,702
David M Gosky · Ohio State University · P30 · FY2021 · CA

Cancer Center Administration

$279,702
David M Gosky · Ohio State University · P30 · FY2022 · CA

Genome Editing Testing Section

$279,537
Cathleen M Lutz · Jackson Laboratory · U42 · FY2019 · OD

MECHANISM OF INTERFERON ACTION

$279,537
University Of California Santa Barbara · R01 · FY2001 · AI

MECHANISM OF INTERFERON ACTION

$279,534
University Of California Santa Barbara · R01 · FY2000 · AI

New tools for the characterization of gene predictions in prokaryote genomes: app

$279,470
Luciano Brocchieri · University Of Florida · R01 · FY2011 · GM

Disease Models and Mechanisms Core

$279,288
Stefan Somlo · Yale University · P30 · FY2019 · DK

Triggering Innate Immunity in Tumor Cells to Overcome Resistance to Immunotherapy

$279,077
Jeffrey J. Ishizuka · Yale University · K08 · FY2021 · CA

Triggering Innate Immunity in Tumor Cells to Overcome Resistance to Immunotherapy

$279,077
Jeffrey J. Ishizuka · Yale University · K08 · FY2020 · CA