Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Medicago truncatula transformation using root explants.

Cynthia Crane1, Richard A Dixon, Zeng-Yu Wang

  • 1Forage Improvement Division, The Samuel Roberts Noble Foundation, Ardmore, OK, USA.

Methods in Molecular Biology (Clifton, N.J.)
|September 22, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Age-dependent epigenetic control of flavonoid metabolism underlies chemical defenses in ancient Ginkgo biloba.

The Plant cell·2026
Same author

Reply to: an assessment of the cytochrome P450 2-hydroxyisoflavanone synthase (2-HIS) crystal structure.

Communications biology·2026
Same author

Genome-wide association study (GWAS) and transcriptome analysis reveal new candidate genes for leaf size in alfalfa.

BMC plant biology·2026
Same author

Genome-Wide Identification and Transcriptomic Analysis of <i>MYB</i> Transcription Factors in Seashore Paspalum Under Salt Stress.

International journal of molecular sciences·2026
Same author

Global Transcriptome Analysis Reveals the Molecular Mechanism Underlying Seed Physical Dormancy Formation in <i>Medicago sativa</i>.

Genes·2025
Same author

ANTHOCYANIDIN REDUCTASE promotes physical dormancy in Medicago truncatula seeds.

Plant physiology·2025
Same journal

Mapping the 3D Chromosome Organization of a Biosynthetic Gene Cluster by Capture Hi-C (CHi-C).

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Mapping the 3D Chromosome Organization of Streptomyces by Hi-C.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

CUT&Tag Epigenomic Profiling of Biosynthetic Gene Clusters in Arabidopsis thaliana.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Rhizobium rhizogenes-Mediated Hairy Root Transformation Protocol for Lotus japonicus and Other Legumes.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Characterization of Bioactive Saponins from Sea Cucumbers.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Methods for Functional Validation of Terpenoid Metabolic Clusters in Nicotiana benthamiana and Aspergillus oryzae.

Methods in molecular biology (Clifton, N.J.)·2026
See all related articles

This study presents an efficient Agrobacterium tumefaciens-mediated transformation protocol for Medicago truncatula roots. This method facilitates functional genomic studies and the recovery of fertile transgenic plants, advancing legume research.

Area of Science:

  • Plant Biology
  • Molecular Biology
  • Genetics

Background:

  • Medicago truncatula is a model legume extensively used for studying root endosymbiotic associations.
  • Understanding symbiotic interactions like nodulation and mycorrhizal colonization is crucial for plant science.
  • Efficient genetic transformation methods are essential for functional genomic studies in model plants.

Purpose of the Study:

  • To describe an efficient Agrobacterium tumefaciens-mediated transformation protocol for Medicago truncatula roots.
  • To enable the generation of transgenic Medicago truncatula plants for functional genomic analysis.
  • To provide a method adaptable for recovering fertile transgenic plants from transformed hairy roots.

Main Methods:

  • Agrobacterium tumefaciens-mediated transformation of Medicago truncatula roots.

Related Experiment Videos

  • Development of a protocol for generating transgenic hairy roots.
  • Adaptation of the protocol for the recovery of fertile transgenic plants.
  • Main Results:

    • An efficient system for generating transgenic Medicago truncatula plants from roots was established.
    • The protocol facilitates Agrobacterium tumefaciens-mediated transformation.
    • The method is adaptable for producing fertile transgenic offspring.

    Conclusions:

    • The described protocol offers an efficient route for genetic modification of Medicago truncatula.
    • This advancement supports functional genomic studies in legumes.
    • The protocol is valuable for producing transgenic Medicago truncatula for research purposes.